Estimates of marker effects for measures of milk flow in the Italian brown Swiss dairy cattle population
© Gray et al.; licensee BioMed Central Ltd. 2012
Received: 20 February 2012
Accepted: 5 October 2012
Published: 23 October 2012
Milkability is a complex trait that is characterized by milk flow traits including average milk flow rate, maximum milk flow rate and total milking time. Milkability has long been recognized as an economically important trait that can be improved through selection. By improving milkability, management costs of milking decrease through reduced labor and improved efficiency of the automatic milking system, which has been identified as an important factor affecting net profit. The objective of this study was to identify markers associated with electronically measured milk flow traits, in the Italian Brown Swiss population that could potentially improve selection based on genomic predictions.
Sires (n = 1351) of cows with milk flow information were genotyped for 33,074 single nucleotide polymorphism (SNP) markers distributed across 29 Bos taurus autosomes (BTA). Among the six milk flow traits collected, ascending time, time of plateau, descending time, total milking time, maximum milk flow and average milk flow, there were 6,929 (time of plateau) to 14,585 (maximum milk flow) significant SNP markers identified for each trait across all BTA. Unique regions were found for each of the 6 traits providing evidence that each individual milk flow trait offers distinct genetic information about milk flow. This study was also successful in identifying functional processes and genes associated with SNPs that influences milk flow.
In addition to verifying the presence of previously identified milking speed quantitative trait loci (QTL) within the Italian Brown Swiss population, this study revealed a number of genomic regions associated with milk flow traits that have never been reported as milking speed QTL. While several of these regions were not associated with a known gene or QTL, a number of regions were associated with QTL that have been formerly reported as regions associated with somatic cell count, somatic cell score and udder morphometrics. This provides further evidence of the complexity of milk flow traits and the underlying relationship it has with other economically important traits for dairy cattle. Improved understanding of the overall milking pattern will aid in identification of cows with lower management costs and improved udder health.
KeywordsMilk flow GWAS Milkability
In dairy cattle, traits influencing efficiency of production can be characterized as production or functional traits. Traits classified as functional, increase efficiency by reducing costs of inputs. Milkability, health, fertility, feed efficiency and calving ease all belong to this group of functional, cost-saving traits .
Milkability has long been recognized as an economically important trait that can be improved through selection [4, 5]. By improving milkability, management costs of milking decrease through reduced labor and improved efficiency of the automatic milking system , which has been identified as an important factor affecting net profit .
In 2005, the Italian Brown Breeders Association (ANARB) made an update to their selection index (TMI) to include milking speed measured as AVGF. However, milking speed is unfavorably correlated with other economically important traits, particularly somatic cell score (SCS, r=0.46) . Therefore with the inclusion of milking speed in the selection index, SCS was also included with a slight negative weight in the TMI. This negative weight was introduced in the TMI to offset the predicted consequence that an increase in milking speed could potentially increase SCS resulting in a possible increase of mastitis .
Gray et al.  showed that a combination of milk flow parameters describing the overall patterns of milk removal would be an advantageous selection strategy for improved milkability, when compared to use of a single variable such as AVGF. Traits previously shown to be unfavorably correlated  with milking speed (SCS, udder score) could respond favorably to selection by including both milking flow and milking time measures in a sub-index with appropriate weights .
By exploiting the advances in molecular genetics and bioinformatics tools an increased understanding of milk flow traits on a molecular level could be achieved. Development of dense SNP marker panels has provided an opportunity to perform genome wide association studies (GWAS) to determine biological differences that exist in an animal’s genetic makeup .
Molecular genetic markers that are associated with phenotypic variation of complex traits, provide information that may be utilized through marker assisted selection  or genomic selection . Using information available from markers in selection can increase the accuracy and efficiency of a breeding program when compared to traditional breeding schemes .
Only a few quantitative trait loci (QTL) have previously been associated with milkability traits, namely milking speed measured on a subjective scale [13, 14]. These milking speed markers explain a fraction of the genetic variance associated with milk flow traits. It is likely that there are more genomic regions associated with milkability traits that have not been unveiled and some of these include genes, regulatory regions or some other sequence of DNA that behaves differently due to a single mutation causing a change in biological mechanisms associated with milk flow. Implementation of a GWAS using a dense 50k marker panel will aid in the discovery of unidentified QTL regions for milking speed traits. Significant markers could potentially represent causative mutations within previously identified genes, functional RNAs or regulatory regions, or more likely are not causative by themselves but in sufficient linkage disequilibrium (LD) to pick up the effect of the nearby causative factor. Identification of candidate gene regions could lead to a better understanding of the biological mechanisms that control milking flow in dairy cattle. Furthermore, differences in the number of identified regions and size of effects for individual SNPs can shed some light on the genetic architecture of milk flow related traits. The objective of this study was to identify SNP markers associated with milk flow traits including total milking time (TMT), ascending time (AT), time of plateau (TP), descending time (DT), maximum milk flow (MMF) and average milk flow (AVGF) by GWAS. As a result chromosomal regions would be identified that could include QTLs for milkability traits that can potentially improve selection based on genomic predictions.
Results and discussion
Summary of heritabilities and reliabilities of estimated breeding values
Reliability of EBV
0.11 ± 0.009
0.02 ± 0.006
0.32 ± 0.016
0.05 ± 0.007
0.42 ± 0.016
0.29 ± 0.014
Summary of markers with largest effects (p < 0.001) including the number of regions and number of chromosomes that they are found in
# of BTA2
# of regions
Combined absolute effect3
Combined relative variance
Among all of the QTL previously mapped in the bovine genome only a few have been identified for milking speed (MSPD) measured on a subjective scale. There are a total of 14 MSPD QTL across 12 BTA identified among Holstein [14–16], Normande , Montbeliarde  and Finnish Ayrshire  dairy breeds. However, there have been no MSPD QTL reported for Brown Swiss. Nevertheless, significant markers identified from this study were located within all previously identified MSPD QTL within other breeds [14–17].
Udder morphometric traits (UT) (teat placement (TPL), udder attachment (UA), udder cleft (UC), udder composite index (UCI), udder depth (UDPTH), udder height (UHT) and udder width (UWDT)) are associated with milk flow traits . It is understood that milk flow may be highly influenced by size, shape and overall confirmation of the udder . Reduced milking performance has been recognized to be associated with larger or slacker teats as well and is influential in change of milking speed and time . For this study all udder morphometric QTL were categorized as a single trait referred to as UT.
Other QTL potentially associated with milk flow are mammary health indicator traits (clinical mastitis (CM), somatic cell count (SCC) and somatic cell score (SCS)). Since most mammary infections are caused by bacterial invasion of the mammary gland through the teat canal cows with larger teat canals are more susceptible to mammary infections. Larger teat canals also increases MMF  and increases in MMF may result in an increased incidence of clinical mastitis. Both SCC and SCS have a positive genetic correlation with milk flow  and are considered to be indicator traits for clinical mastitis, therefore QTL for all three traits (SCC, SCS and CM) were considered in the analysis.
There is an unfavorable relationship between production traits (i.e. milk yield (MY) and 305 day lactation milk yield MY305) and milking time  thus QTL for these traits could possibly be co-located with significant markers for milk flow traits. Numerous milk yield QTL (MY, MY305, etc.) have been previously identified across the bovine genome in several breeds. Only MY QTL previously identified for Brown Swiss were here considered .
Ascending time (AT)
There were 9,425 SNP marker effects that were significantly different from 0 (outside the 95% C.I.). Markers with the largest effect (n = 100) identified 79 distinct regions. Among these regions 41 were within QTL related to milk flow previously identified, including mastitis, udder and milk production QTL. Four of these regions located in BTA4 (70.7 to 70.9 Mb), BTA7 (52.9 to 56.5 Mb, 81.6 Mb) and BTA23 (21.3 to 23.7 Mb) were within previous MSPD QTL. The variance explained by these single regions was 0.123%, 0.06%, 0.05%, and 0.05% of the total genomic variance for AT, respectively. MSPD QTL that were previously identified in Holstein, French dairy cattle (Holstein, Normande and Montbeliarde) and Finnish Ayrshire mapped within BTA7 (35.9 – 106 Mb) , BTA23 (19.4-28.0 Mb)  and BTA4 (57.0 – 75.3 Mb) . The largest marker effect (0.06 s) for AT (Hapmap38595-BTA-36915, 44.2 Mb) was located within a region on BTA15 (39.4 – 44.2 Mb) and explained 0.42% of the additive variance. UT (40.1 – 47.9 Mb)  and SCS (39.1 – 41.1 Mb)  QTL also mapped to this region on BTA15.
Time at plateau (TP)
Time at plateau (TP) had the least number of effects that were significantly different from 0 (outside the 95% C.I.) at 6,929 markers across the entire genome. Among the 100 largest effects for TP there were 78 regions of which 41 were within QTL previously identified for traits associated with milking production traits. Two of these regions located in BTA6 (118.6 Mb) and BTA23 (35.5 to 38.2 Mb) were within MSPD QTL previously identified for French dairy cattle and Holstein on BTA6 (99.2 – 113 Mb)  and BTA23 (19.4-36.7 Mb) , respectively. The markers associated with MSPD QTL on BTA6 and BTA23 explained 0.06% and 0.21% of the genomic variance, respectively. The largest marker effect (0.18 s) was located on BTA25 (ARS-BFGL-NGS-114447, 40.8 Mb) explaining 0.12% of additive variance for TP. This marker mapped within SCS, UT (39.1 – 41.1 Mb) and MY (32.9 – 43.9 Mb) [14, 24] QTL previously identified.
Descending time (DT)
Descending time (DT) had 13,590 markers significantly different from 0 (outside the 95% C.I.). The 100 markers with largest effects identified 76 regions of which 36 were within QTL of interest. Descending time had the largest number of regions mapping within MSPD QTL. Three regions located in BTA7 (81.6 Mb, 93.1 to 93.3 Mb and 102.9 Mb) explaining a total of 0.23% of the genomic variance were within the MSPD QTL reported to be on BTA7 (35.9 – 106 Mb)  and another three regions located in BTA4 (70.7 to 70.9), BTA19 (52.3 Mb) and BTA23 (20.0 – 23.0) were within MSPD QTL explaining 0.11%, 0.06% and 0.05% of the total genomic variance, respectively. These QTL were previously identified on BTA4 (57.0 – 75.3 Mb) , BTA19 (51.5 – 53.5 Mb)  and BTA23 (19.4-36.7.0 Mb) . The largest effect for DT (0.66 s) was the same marker that was largest for TMT, MMF and AVGF (Hapmap27408-BTA-143963, BTA6, 42.5 Mb) and explained 0.19% of the total genomic variance for DT. This marker was within 3 QTL identified in Holstein-Friesian including CM (26.7 – 65.9 Mb)  SCS (41.4 – 43.4 Mb) , and UT (34.6 – 44.2 Mb) .
Total milking time (TMT)
Total milking time is essentially a combination of AT, TP and DT. There were 11,612 markers across all 29 BTA with predicted effects that were significantly different from 0 (outside the 95% C.I.) for TMT. The 100 largest markers effect were located in 77 distinct regions of which 37 with at least one marker within a previously identified QTL for traits associated with milk flow. Among these regions, there were 4 regions in BTA7 (52.9 to 56.5 Mb), BTA8 (55 Mb) and BTA23 (21.3 – 23.7 Mb and 35.5 to 38.2 Mb) within QTL previously identified for MSPD in Holstein, French dairy cattle and Finnish Ayrshire which explained 0.06%, 0.05%, 0.07% and 0.05% of the genomic variance for TMT, respectively. These QTL were also among other milking flow related QTL that were previously identified within BTA7 (35.9 – 106 Mb) , BTA8 (20.0 - 55.1 Mb)  and BTA23 (19.4-28.0 Mb)  including SCS, MY, CM and UT. Similar to DT the marker with the largest effect (0.84 s) which explained 0.21% of genomic variance for TMT was on BTA6 (Hapmap27408-BTA-143963, 42.5 Mb).
Maximum milk flow (MMF)
Maximum milk flow (MMF) had the largest number of significant SNPs (14,585). There were 75 regions harboring the 100 largest markers for MMF. Of these regions 34 mapped within previously discovered QTL. Three of these regions on BTA4 (70.7 to 70.9), BTA7 (81.6 Mb) and BTA23 (21.3 to 23.7 Mb) explaining 0.12%, 0.04%, 0.07% of the genomic variance for MMF mapped within MSPD QTL on BTA4 (57.0 – 75.3 Mb) , BTA7 (35.9 – 106 Mb)  and BTA23 (19.4-36.7 Mb) . The largest absolute effect (0.011 kg/min) was identified on BTA6 (Hapmap27408-BTA-143963, 42.5 Mb) and explained 0.22% of genomic variance for MMF similarly to TMT and DT.
Average milk flow (AVGF)
Average milk flow (AVGF) had 14,178 significant markers across the entire genome. Among the 100 markers with largest effects there were 77 regions of which 33 within QTL of interest. Regions on BTA7 (81.6 Mb) and BTA23 (21.3 to 23.7 Mb) explained 0.05% and 0.06% of genomic variance for AVGF and were within two MSPD QTL (35.9 – 106 Mb)  (19.4-36.7 Mb)  on BTA7 and BTA23, respectively. The marker with the largest effect (0.006 kg/min) was also the same marker identified as having the largest effect for TMT, DT and MMF on BTA6 (Hapmap27408-BTA-143963, 42.5 Mb) and explained 0.23% of the genomic variance for AVGF.
Common markers among milk flow traits
As mentioned above the largest effect for TMT, DT, MMF and AVGF was a single marker (Hapmap27408-BTA-143963, 42.5 Mb) on BTA6 which was within a QTL rich region of 3 QTL for CM (26.7 – 65.9 Mb)  SCS (41.4 – 43.4 Mb) , and UT (34.6 – 44.2 Mb) . Although this marker was not the largest effect for AT and TP it was within the top 40 largest effects. Further investigation within a 5 Mb region on each side of this marker revealed no annotated genes with obvious connection to milk flow.
While there were several common SNPs identified among the 100 with largest effect for each of the traits, additional unique SNPs were identified for each of the milk flow traits with TP having the most unique markers. This indicates that while milk flow traits show a medium to large genetic correlation  there might be regions of the genome that are uniquely associated with each trait.
A large number of markers identified for milk flow traits were in regions where QTL for MSPD, MY, SCC, SCS, UT and CM, were previously found (Additional file 1: Table S1), indicating that milking time is a complex trait that either incorporates many factors, influences several other traits or a combination of both. Although associations between milking speed, SCS, and clinical mastitis incidence has been somewhat controversial, it is generally accepted that fast milking whether measured subjectively [16, 27] or electronically [28, 29] is associated with higher levels of SCS. One possible explanation for this biological correlation could be the result of increased teat sphincter diameter . This could result in an increase in milk flow and subsequently allow more pathogens to enter the mammary gland causing infection of the udder.
Finding markers within QTL associated with udder morphometric traits was expected. It has been reported that udder morphometric traits including increased udder size and teat size tend to negatively influence the efficiency of the milking machine therefore increasing the amount of time it takes to milk [18, 30].
Complexity of milk flow traits
Markers within each milk flow trait were sorted based on their absolute effect for the given trait of interest. Markers were isolated from the complete panel in subsets of 25, 50, 300, 3,000 and 10,000 SNPs with the largest effect. Genomic breeding values and genomic variances were then obtained from these subsets of markers.
Figure 3B depicts the proportion of the correlation coefficient depicted in 3A recovered by EBVs predicted from phenotypic data and DGVs obtained from subsets of markers with the largest effects for each of the milk flow traits, namely 25, 50, 300, 3,000 and 10,000 SNPs. In the figure correlation coefficient between EBVs and DGV predicted from 25 markers ranged from 0.13 to 0.33 which explains 19% to 46% of the correlation between EBV and DGV predicted using all of the markers, as illustrated in Figure 3A. There appeared to be two traits, AT and DT, for which panels of 25 markers captured twice as much correlation than, TMT, TP, MMF and AVGF. While it is possible that this may be the result of the markers capturing QTL with larger effects this is unlikely due to the low heritability that was estimated for these traits. The large proportion of the correlation explained within AT and DT is most likely the result of poor reliability for EBV obtained from phenotypic data. Poor reliable estimates of EBVs resulted in a lower overall correlation between the EBV and DGV (Figure 3A). Given that the correlation is lower in general it is possible that a smaller number of markers would explain a larger proportion of the correlation.
Among the other traits, with moderate heritabilities, breeding values obtained from 25 markers captured approximately one-fifth of the overall correlation. Increasing the number of markers from 25 to 3000 increased the correlation with approximately 0.45 for all traits. Correlations between EBVs and DGVs predicted from more than 3000 markers plateaued revealing a non-linear relationship between correlations estimated from differing number of markers, contrary to what would be expected under a pure polygenic architecture. This offers possible evidence for the presence of moderate size QTL, associated with milk flow.
Proportion of genomic variance that can be explained with different number of markers with largest effects
# of markers
Number of markers within genes or regulatory region and the proportion of variation that can be explained by markers within genes
Number of markers with largest effects
All significant markers
Total number of Markers within Gene or Regulatory Region
Proportion of Variation explained from Markers within genes and regulatory regions
DGVs were predicted from significant marker effects within coding regions (DGVgene), and were compared to DGVs predicted from all significant markers (DGVsig) without respect to whether they were in a coding region or not. The median proportions DGVsig that can be explained by DGVgene were 0.35, 0.39, 0.73, 0.20, 0.43 and 0.34 for TMT, AT, TP, DT, MMF and AVGF, respectively. Time at plateau was the only trait where markers within coding regions explained a larger proportion of the breeding value than markers within non-coding regions. Significant markers for TP within genes had larger effects than the remaining significant markers suggesting that the set of markers used in this study may have in fact identified genes that influence TP.
Functional processes associated to SNP affecting milk flow
Within the mammary gland, milk is initially secreted into small sacs called alveoli, from which it is ejected during milking . Mammary alveoli are surrounded by smooth muscle (myoepithelial) cells , which are a prominent target cell for oxytocin . Oxytocin stimulates contraction of myoepithelial cells, causing milk to be ejected into the ducts and cisterns . Smooth muscle contractions in vertebrates are initiated by an increase in intracellular calcium . In turns the intracellular calcium binds with calmodulin, which then binds and activates myosin light-chain kinase . The calcium-calmodulin-myosin light-chain kinase complex phosphorylates myosin initiating contraction and activating the myosin ATPase . By selecting the 1,000 markers with largest effects in AT, TP, DT, TMT, MMF and AVGF a total of 452 unique genes were identified using the R package FunctSNP. Performing a functional annotation through DAVID , calmodulin-binding was the most significant functional category identified through sp_pir_keywords (nominal P - Value of 7.3E-3). A further search of the universal protein database  identified the ADCY (adenilate cyclase) gene (BTA4 76869665.76969459), a gene implicated in calmodulin induced events and calcium signaling pathway . Furthermore, a significant KEGG pathway (nominal P - Value of 1.2E-2) was identified with 11 genes related to the calcium-signaling pathway (Additional file 3: Figure S1). Among these genes was the 5-hydroxytryptamine receptor 2A HTR2A, (BTA12 16823524.16889281) a serotonin receptor. Serotonin is a biogenic amine that is synthesized both in the enteric nervous system and the central nervous system  and the serotonergic system is involved in the regulation of oxytocin release . Results the current GWAS are only suggestive and further investigation should be carried out to confirm or rule out our findings, but the current study identified potential areas for future studies targeted at particular pathways that include genes that may influence milk flow.
In this study we have identified significant markers for six milk flow traits. There was an average of 11,720 markers significant for each of the milk flow traits assessed with a majority of markers having a small effect. These traits should be considered polygenic; however, we were able to collocate 10 regions with largest effects to seven QTL previously identified for milking speed. Each trait had significant markers that were in same region as MY and udder confirmation QTL. Phenotypic and genetic relationships between milking speed and mastitis, or its indicator traits, have been controversial, among the largest marker effects for each of the milk flow traits, there was an association with udder health QTL (SCC, SCS, or clinical mastitis) and milking speed QTL. Other significant regions for each of the traits were also identified but did not appear to be near any previously associated QTL or annotated gene requiring additional investigation to determine if these regions capture additional information that would be beneficial in understanding the biological mechanisms involved in milk flow.
Genetic improvement of milk flow using genomic tools has yet to be implemented. Whole genome selection methods should be considered as an alternative to using traditional selection methods or even considering the use of a subset of significant markers. This study verified that milk flow traits are complex and by including all information available from a SNP marker panel for all six milk flow traits in a selection index, milk flow pattern is taken into account on a genomic level, therefore it can be more advantageous in improving selection strategy. Incorporating all traits should decrease milk time while controlling for milk yield as well as control for clinical mastitis and its indicator traits of SCC and SCS and also other traits associated with udder size through indirect correlated response to selection in Italian Brown Swiss.
Data for this study were provided by ANARB and included information spanning a 12 year period (1997 to 2008).
Description of traits and animals
The dataset included 37,213 cows, daughters of 2,361 sires and 30,231 dams with pedigree information spanning seven generations. Milking release was measured once for each cow using a portable milk flow recorder (LactoCorder, WMB AG, Balgach, Switzerland). Milk flow characteristics were detected every 0.7 s and saved at intervals of 2.8 s. Milk flow was divided into six phases: 1) AT, period spanning milk flow greater than 0.5 kg/min until TP; 2) TP, period of steady milk flow; 3) DT, period from the end of TP until milk flow below 0.2 kg/min; 4) overmilking time, period between milk flow below 0.2 kg/min and group removal; 5) stripping time, period at end of milking, with milk flow greater than 0.2 kg/min and lasting for at least 4.2 s; and 6) overmilking time after stripping, period after stripping between a milk flow below 0.2 kg/min and the group removal after stripping time (Figure 2). The overall sum of all the periods corresponds to TMT. Additionally, MMF was recorded as the maximum flow preceding TP. The six traits investigated in this study were: TMT, AT, TP, DT, MMF and average milk flow (AVGF). A complete description of editing and collection procedures for these traits can be found in Gray et al. .
There were 1351 bulls genotyped from the Italian Brown Swiss population that had direct relationship ties with cows that have measurements of milk flow. Average progeny size for the bulls in the dataset was 28 ± 2.6 daughters with milk flow measurements available for analysis. Breeding values for the genotyped bulls were estimated using a multivariate 6-trait animal model similar to the model described in Gray et al. . Breeding values were then de-regressed free from parental averages .
Number of markers per chromosome
Number of markers
Markers within coding regions were flagged, in an effort to identify the proportion of significant markers that may target functional mutations within annotated genes.
We extracted coordinates for coding regions from the GFF3 file for Bos taurus assembly Btau 4.0 file  (http://www.ensembl.org, Btau_4.0; April 2010), 500 kb upstream and downstream of each gene were taken as regulatory regions.
SNP association tests
Shrinkage is often employed in QTL mapping when the number of markers to test is much larger than the individual observations . Briefly shrinkage methods work by forcing some of the marker effects with trivial effects to 0. Different approaches for shrinking are available allowing fitting all markers simultaneously. Although not necessarily often these methods are implemented in a Bayesian version, which effectively, allows more flexibility in the strength, with which each marker is pushed toward 0. In the Bayesian-LASSO a double exponential prior is assigned to SNP variances . Alternatively, inverted χ2 priors can be used . Here we report on a GWAS for milk flow traits using regression through Bayesian LASSO.
Where y represents de-regressed breeding values, μ represents a mean; Si is the random polygenic effect for the sires was fitted to prevent spurious associations due to population structure and had variance estimated from the data (Aσ2s) with A representing the expected (based on pedigree) relationship matrix among the sires  with a SNP genotype of the ith sire represented as x i (−1, 0, and 1); β represents the regression coefficient for the SNP or the allele substitution effect and eij is the random residual (Iσ2e) for each observation. A Gibbs sampling algorithm for all traits was implemented in R (R Development core Team 2009). For each analysis a single chain of 100,000 iterations was run with a burn-in period of 30,000 iterations. Although values for the λ shrinkage parameter can be sampled within each chain from their gamma prior distribution, in the final analysis we fixed the values of lambda based on the average of 5 shorter exploratory chains, which were run for each trait (50,000 iterations). Values of the λ parameters were similar across traits ranging from 21 for TMT, to 37 for AT.
For all analyses, thinning was applied and samples were stored every 30 iterations. Convergence of each chain was assessed both by visual inspection of the trace and the use of estimates of effective sample size for variances obtained through the coda package in R . Inferences on the parameters were made from the mean of the posterior samples after burn-in.
An alternative method commonly referred to as Bayes Cπ  in which explicit model selection is employed and the proportion of markers with null effect is estimated from the data was employed to support the results obtained from the permutation method described above. Both methods attained similar results with an estimate of π (the proportion of null markers) ranging from 59% to 67% in the Bayes Cπ analysis in line with the reshuffling approach (data not shown).
Shrinkage mapping is an efficient tool for whole genomic evaluations due to its scalability to large sets of markers, when compared to interval mapping LA  or LDLA analyses [51, 52]. In several Bayesian shrinkage analyses no explicit model selection is performed and the equivalent result is obtained implicitly through the shrinkage process. As a result detection of QTL is performed by visual inspection of the resulting Manhattan plot. Formal methods of testing marker significance can also be used employing a posterior likelihood ratio test for the model with and without a particular marker included . Alternatively non-parametric methods based on data shuffling can be employed. In the current study a permutation within chain was employed as proposed by Che and Xu . Briefly, in their permutation strategy, at every h iteration of the current Markov chain the data is shuffled, where 1 < h < L with L being the length of the Markov Chain. For h =L permutation is equivalent to across chain permutation, while h=1 implies permutation in each iteration. The reshuffled chain then provides the 0.25 α × 100% and the (1–0.25 α) × 100% percentiles used as critical values for the analysis . The within chain permutation is a strategy to obtain the posterior of the markers effect (regression coefficients) under the null model. While conceptually the method is no different from across chain permutation, the number of chains needed for the analysis is reduced to two. After an exploratory investigation, the permutation parameter h was set to 3 for the current analysis. Permutated marker effects were obtained from the posterior means of a 250,000 iteration chain.
Evaluation of markers for prediction
Number of animals in discovery and prediction data set
Total milking time
Time of plateau
Maximum milk flow
Average milk flow
Correlations were estimated between the EBV and DGV for each of the traits within the prediction set to demonstrate the association between breeding values obtained from marker effects and the best estimate of the true breeding values. There is a correlation between additive genetic variance σ2g and genomic variance σ2g with the latter proportional to the first. For the LASSO model employed in this investigation the relationship is as follow . In our analysis the posterior mean of each SNP effect was used to obtain genomic merit of individuals. Then the proportion of total genomic variance explained by subset of markers was obtained similarly to what proposed by Peters et al. . Specifically, the overall genomic variance was obtained as the variance of the estimated DGVs, and the variance of subset of markers was obtained as the variance of DGVS calculated from the specific subset employed.
Functional annotation pathways search and the identification of potential candidate genes were performed through DAVID . Identification of unique genes was perfomed on the bovine assembly Btau_4.0 (http://www.ensembl.org, Btau_4.0; Nov 2011) using the R package FunctSNP.
The research leading to these results has received funding from the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement no. 222664 (“Quantomics”). This article reflects only the author’s views and the European Community is not liable for any use that may be made of the information contained herein. MD was supported by Austrian Science Fund (FWF): project number L403-B11 to Christian Schlötterer.
- Groen AF, Steine T, Colleau JJ, Pedersen J, Pribyl J, Reinsch N: Economic values in dairy cattle breeding, with special reference to functional traits. Report of an EAAP working group. Livest Prod Sci. 1997, 49: 1-21. 10.1016/S0301-6226(97)00041-9.View ArticleGoogle Scholar
- Gade S, Stamer E, Junge W, Kalm E: Estimates of genetic parameters for milkability from automatic milking. Livest Sci. 2006, 104: 135-146. 10.1016/j.livsci.2006.04.003.View ArticleGoogle Scholar
- Gray KA, Vacirca F, Bagnato A, Samore AB, Rossoni A, Maltecca C: Genetic evaluations for measures of the milk-flow curve in the Italian Brown Swiss population. J Dairy Sci. 2011, 94: 960-970. 10.3168/jds.2009-2759.View ArticlePubMedGoogle Scholar
- Bruckmaier R, Rothenanger E, Blum J: Milking characteristics in dairy cows of different breeds from different farms and during the course of lactation. J Anim Breed Genet. 1995, 112: 293-302. 10.1111/j.1439-0388.1995.tb00569.x.View ArticleGoogle Scholar
- Miller RH, Pearson RE, Weinland BT, Fulton LA: Genetic parameters of several measures of milk flow-rate and milking time. J Dairy Sci. 1976, 59: 957-964. 10.3168/jds.S0022-0302(76)84304-4.View ArticlePubMedGoogle Scholar
- Meyer K, Burnside EB: Scope for a subjective assessment of milking speed. J Dairy Sci. 1987, 70: 1061-1068. 10.3168/jds.S0022-0302(87)80112-1.View ArticleGoogle Scholar
- Ghiroldi S, Nicoletti C, Santus E, Rossoni A, Bagnato A: ITE: the new selection index for the italian brown swiss. Proc Int Meet Uppsala, Sweden Interbull Bulletin. 2005, 33: 222-226.Google Scholar
- VanRaden PM: Efficient methods to compute genomic predictions. J Dairy Sci. 2008, 91: 4414-4423. 10.3168/jds.2007-0980.View ArticlePubMedGoogle Scholar
- Matukumalli LK, Lawley CT, Schnabel RD, Taylor JF, Allan MF, Heaton MP, O’Connell J, Moore SS, Smith TPL, Sonstegard TS, Van Tassell CP: Development and characterization of a high density SNP genotyping assay for cattle. PLoS One. 2009, 4 (4): e5350-10.1371/journal.pone.0005350.PubMed CentralView ArticlePubMedGoogle Scholar
- Dekkers JCM: Commercial application of marker- and gene-assisted selection in livestock: strategies and lessons. J Anim Sci. 2004, 82: E313-E328.PubMedGoogle Scholar
- Goddard ME, Hayes BJ: Mapping genes for complex traits in domestic animals and their use in breeding programmes. Nat Rev Genet. 2009, 10: 381-391. 10.1038/nrg2575.View ArticlePubMedGoogle Scholar
- VanRaden PM, Van Tassell CP, Wiggans GR, Sonstegard TS, Schnabel RD, Taylor JF, Schenkel FS: Invited review: reliability of genomic predictions for North American Holstein bull. J Dairy Sci. 2009, 92: 16-24. 10.3168/jds.2008-1514.View ArticlePubMedGoogle Scholar
- Hiendleder S, Thomsen H, Reinsch N, Bennewitz J, Leyhe-Horn B, Looft C, Xu N, Medjugorac I, Russ I, Kuhn C, et al: Mapping of QTL for body conformation and behavior in cattle. J Hered. 2003, 94: 496-506. 10.1093/jhered/esg090.View ArticlePubMedGoogle Scholar
- Schrooten C, Bink MCAM, Bovenhuis H: Whole genome scan to detect chromosomal regions affecting multiple traits in dairy cattle. J Dairy Sci. 2004, 87: 3550-3560. 10.3168/jds.S0022-0302(04)73492-X.View ArticlePubMedGoogle Scholar
- Schrooten C, Bovenhuis H, Coppieters W, Van Arendonk JAM: Whole genome scan to detect quantitative trait loci for conformation and functional traits in dairy cattle. J Dairy Sci. 2000, 83: 795-806. 10.3168/jds.S0022-0302(00)74942-3.View ArticlePubMedGoogle Scholar
- Boichard D, Grohs C, Bourgeois F, Cerqueira F, Faugeras R, Neau A, Rupp R, Amigues Y, Boscher MY, Leveziel H: Detection of genes influencing economic traits in three French dairy cattle breeds. Genet Sel Evol. 2003, 35: 77-101. 10.1186/1297-9686-35-1-77.PubMed CentralView ArticlePubMedGoogle Scholar
- Elo KT, Vilkki J, de Koning D-J, Velmala RJ, Mäki-Tanila AV: A quantitative trait locus for live weight maps to bovine Chromosome 23. Mamm Genome. 1999, 10: 831-835. 10.1007/s003359901098.View ArticlePubMedGoogle Scholar
- Robert WB, McDaniel BT: Relationships of udder conformation with labor and machine inputs to milk harvest in dairy cattle. J Dairy Sci. 1979, 62: 475-485. 10.3168/jds.S0022-0302(79)83269-5.View ArticleGoogle Scholar
- Grindal RJ, Hillerton JE: Influence of milk flow-rate on new intramammary infection in dairy-cows. J Dairy Res. 1991, 58: 263-268. 10.1017/S0022029900029848.View ArticlePubMedGoogle Scholar
- Appleman RD: Quantifying the genetic effects on the anatomy of the streak canal. In Proc. 6th Int. Conf. Cattle Di. 1970, 104:Google Scholar
- Bagnato A, Schiavini F, Rossoni A, Maltecca C, Dolezal M, Medugorac I, Solkner J, Russo V, Fontanesi L, Friedmann A, et al: Quantitative trait loci affecting milk yield and protein percentage in a three-country Brown Swiss population. J Dairy Sci. 2008, 91: 767-783. 10.3168/jds.2007-0507.View ArticlePubMedGoogle Scholar
- Ashwell MS, Heyen DW, Sonstegard TS, Van Tassell CP, Da Y, VanRaden PM, Ron M, Weller JI, Lewin HA: Detection of quantitative trait loci affecting milk production, health, and reproductive traits in holstein cattle. J Dairy Sci. 2004, 87: 468-475. 10.3168/jds.S0022-0302(04)73186-0.View ArticlePubMedGoogle Scholar
- Rupp R, Boichard D: Genetics of resistance to mastitis in dairy cattle. Vet Res. 2003, 34: 671-688. 10.1051/vetres:2003020.View ArticlePubMedGoogle Scholar
- Harder B, Bennewitz J, Reinsch N, Thaller G, Thomsen H, Kühn C, Schwerin M, Erhardt G, Förster M, Reinhardt F, Kalm E: Mapping of quantitative trait loci for lactation persistency traits in German Holstein dairy cattle. J Anim Breed Genet. 2006, 123: 89-96. 10.1111/j.1439-0388.2006.00577.x.View ArticlePubMedGoogle Scholar
- Klungland H, Sabry A, Heringstad B, Olsen HG, Gomez-Raya L, Våge DI, Olsaker I, Ødegård J, Klemetsdal G, Schulman N: Quantitative trait loci affecting clinical mastitis and somatic cell count in dairy cattle. Mamm Genome. 2001, 12: 837-842. 10.1007/s00335001-2081-3.View ArticlePubMedGoogle Scholar
- Daetwyler HD, Schenkel FS, Sargolzaei M, Robinson JA: A genome scan to detect quantitative trait loci for economically important traits in Holstein cattle using two methods and a dense single nucleotide polymorphism map. J Dairy Sci. 2008, 91: 3225-3236. 10.3168/jds.2007-0333.View ArticlePubMedGoogle Scholar
- Lund MS, Guldbrandtsen B, Buitenhuis AJ, Thomsen B, Bendixen C: Detection of quantitative trait loci in Danish Holstein cattle affecting clinical mastitis, somatic cell score, udder conformation traits, and assessment of associated effects on milk yield. J Dairy Sci. 2008, 91: 4028-4036. 10.3168/jds.2007-0290.View ArticlePubMedGoogle Scholar
- Samore AB, Groen AF, Boettcher PJ, Jamrozik J, Canavesi F, Bagnato A: Genetic correlation patterns between somatic cell score and protein yield in the Italian Holstein-Friesian population. J Dairy Sci. 2008, 91: 4013-4021. 10.3168/jds.2007-0718.View ArticlePubMedGoogle Scholar
- Zwald NR, Weigel KA, Chang YM, Welper RD, Clay JS: Genetic evaluation of dairy sires for milking duration using electronically recorded milking times of their daughters. J Dairy Sci. 2005, 88: 1192-1198. 10.3168/jds.S0022-0302(05)72785-5.View ArticlePubMedGoogle Scholar
- White J, Vinson W: Relationships among udder characteristics, milk yield, and nonyield traits. J Dairy Sci. 1975, 58: 729-738. 10.3168/jds.S0022-0302(75)84635-2.View ArticleGoogle Scholar
- Schennink A, Stoop WM, Visker M, Heck JML, Bovenhuis H, Van Der Poel JJ, Van Valenberg HJF, Van Arendonk JAM: DGAT1 underlies large genetic variation in milk fat composition of dairy cows. Anim Genet. 2007, 38: 467-473. 10.1111/j.1365-2052.2007.01635.x.View ArticlePubMedGoogle Scholar
- Hayes BJ, Pryce J, Chamberlain AJ, Bowman PJ, Goddard ME: Genetic architecture of complex traits and accuracy of genomic prediction: coat colour, milk-Fat percentage, and type in holstein cattle as contrasting model traits. PLoS Genet. 2010, 6: e1001139-10.1371/journal.pgen.1001139.PubMed CentralView ArticlePubMedGoogle Scholar
- Bruckmaier RM, Blum JW: Oxytocin release and milk removal in ruminants. J Dairy Sci. 1998, 81: 939-949. 10.3168/jds.S0022-0302(98)75654-1.View ArticlePubMedGoogle Scholar
- Bruckmaier RM, Hilger M: Milk ejection in dairy cows at different degrees of udder filling. J Dairy Res. 2001, 68: 369-376.View ArticlePubMedGoogle Scholar
- Bruckmaier RM, Blum JW: Simultaneous recording of oxytocin release, milk ejection and milk flow during milking of dairy cows with and without prestimulation. J Dairy Res. 1996, 63: 201-208. 10.1017/S0022029900031708.View ArticlePubMedGoogle Scholar
- Jiang H, Stephens NL: Calcium and smooth muscle contraction. Mol Cell Biochem. 1994, 135: 1-9. 10.1007/BF00925956.View ArticlePubMedGoogle Scholar
- Goodswen SJ, Gondro C, Watson-Haigh NS, Kadarmideen HN: FunctSNP: an R package to link SNPs to functional knowledge and dbAutoMaker: a suite of perl scripts to build SNP databases. BMC Bioinforma. 2010, 11: 311-10.1186/1471-2105-11-311.View ArticleGoogle Scholar
- Huang DW, Sherman BT, Zheng X, Yang J, Imamichi T, Stephens R, Lempicki RA: Current protocols in bioinformatics. Extracting biological meaning from large gene lists with DAVID. John Wiley & Sons, Inc; 2002.Google Scholar
- Universal protein database. [http://www.uniprot.org]
- Ross EM, Gilman AG: Biochemical properties of hormone-sensitive adenylate cyclase. Annu Rev Biochem. 1980, 49: 533-564. 10.1146/annurev.bi.49.070180.002533.View ArticlePubMedGoogle Scholar
- Lam DD, Garfield AS, Marston OJ, Shaw J, Heisler LK: Brain serotonin system in the coordination of food intake and body weight. Pharmacol Biochem Behav. 2010, 97: 84-91. 10.1016/j.pbb.2010.09.003.View ArticlePubMedGoogle Scholar
- Yoshida M, Takayanagi Y, Inoue K, Kimura T, Young LJ, Onaka T, Nishimori K: Evidence that oxytocin exerts anxiolytic effects via oxytocin receptor expressed in serotonergic neurons in mice. J Neurosci. 2009, 29: 2259-2271. 10.1523/JNEUROSCI.5593-08.2009.View ArticlePubMedGoogle Scholar
- Garrick DJ, Taylor JF, Fernando RL: Deregressing estimated breeding values and weighting information for genomic regression analyses. Genet Sel Evol. 2009, 41: 55-10.1186/1297-9686-41-55.PubMed CentralView ArticlePubMedGoogle Scholar
- BovineGenome.org: The bovine genome database. [https://genomes.arc.georgetown.edu/drupal/bovine/?q=download_chromosome_gff3]
- Yi N, Xu S: Bayesian LASSO for quantitative trait loci mapping. Genetics. 2008, 179: 1045-10.1534/genetics.107.085589.PubMed CentralView ArticlePubMedGoogle Scholar
- De los Campos G, Naya H, Gianola D, Crossa J, Legarra A, Manfredi E, Weigel K, Cotes JM: Predicting quantitative traits with regression models for dense molecular markers and pedigree. Genetics. 2009, 182: 375-385. 10.1534/genetics.109.101501.PubMed CentralView ArticlePubMedGoogle Scholar
- Cleveland M, Forni S, Deeb N, Maltecca C: Genomic breeding value prediction using three Bayesian methods and application to reduced density marker panels. BMC Proc. 2010, 4: S6-10.1186/1753-6561-4-S1-S6.PubMed CentralView ArticlePubMedGoogle Scholar
- Plummer M, Best N, Cowles K, Vines K: CODE: convergence diagnosis and output analysis for MCMC. R News. 2006, 6: 7-11.Google Scholar
- Habier D, Fernando R, Kizilkaya K, Garrick D: Extension of the bayesian alphabet for genomic selection. BMC Bioinforma. 2011, 12: 186-10.1186/1471-2105-12-186.View ArticleGoogle Scholar
- Jansen RC: Interval mapping of multiple quantitative trait loci. Genetics. 1993, 135: 205.PubMed CentralPubMedGoogle Scholar
- Farnir F, Grisart B, Coppieters W, Riquet J, Berzi P, Cambisano N, Karim L, Mni M, Moisio S, Simon P: Simultaneous mining of linkage and linkage disequilibrium to fine map quantitative trait loci in outbred half-sib pedigrees: revisiting the location of a quantitative trait locus with major effect on milk production on bovine chromosome 14. Genetics. 2002, 161: 275.PubMed CentralPubMedGoogle Scholar
- Zhao HH, Fernando RL, Dekkers JCM: Power and precision of alternate methods for linkage disequilibrium mapping of quantitative trait loci. Genetics. 1975, 2007: 175.Google Scholar
- Maltecca C, Gray KA, Weigel KA, Cassady JP, Ashwell M: A genome-wide association study of direct gestation length in US Holstein and Italian Brown populations. Anim Genet. 2011, 42: 585-591. 10.1111/j.1365-2052.2011.02188.x.View ArticlePubMedGoogle Scholar
- Che X, Xu S: Significance test and genome selection in Bayesian shrinkage analysis. Int J Plant Genomics. 2010, 2010: 10.1155/2010/893206.Google Scholar
- Peters SO, Kizilkaya K, Garrick DJ, Fernando RL, Reecy JM, Weaber RL, Silver GA, Thomas MG: Bayesian genome wide association analyses of growth and yearling ultrasound measures of carcass traits in Brangus heifers. J Anim Sci. 2012, 10.2527/jas.2011-4507.Google Scholar
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