Location: Reproduction Research2009 Annual Report
1a. Objectives (from AD-416)
Objective 1: Develop genetic tests which can be used as tools to improve selection in commercial swine populations for important production traits. Objective 2: Determine interactions among traits, parental origin of alleles, loci and/or environment to better understand the basis of genetic correlations, inheritance of complex traits and to more accurately formulate selection plans in swine. Objective 3: Utilize the knowledge gained from objective 2 and from USMARC collaborators in conjunction with the swine genome sequence to identify the causative genes underlying QTL.
1b. Approach (from AD-416)
The goal of this research is to ensure US swine producers are a competitive source of pork products by providing the genetic information necessary to maintain superior production levels. The approach will use genetic markers and genomic technologies to understand how the genome regulates animal performance and determine the molecular basis behind non-additive genetic effects. Availability of the draft swine genome sequence will allow continuation of research on genomic regions affecting components of reproductive performance, growth, and carcass quality to move faster and more efficiently. Future studies will include a broader list of phenotypes including metabolic parameters to understand nutrient utilization, animal disposition and incidence of disease during natural outbreaks in the population. This project will use genomic approaches in combination with extensively phenotyped swine populations to identify genetic markers associated with production traits and understand these complex biological processes. Our approach will be to conduct genome-wide QTL scans and then fine map these QTL and develop SNP markers in tight linkage with the causative polymorphisms. QTL scans will be conducted in subsets of the USMARC BX swine population that have been extensively phenotyped for a wide variety of traits. This will permit a more complete biological understanding of each QTL region. Follow-up studies on QTL will be conducted in the BX population on larger groups of animals that may be phenotyped for a specific set of traits. Standard QTL analyses will first be conducted followed by statistical models to identify components to nonadditive genetic variation affecting performance such as intra-locus (dominance and imprinting) and inter-locus (epistatic) interactions. These analyses will also yield valuable information about pleiotropic effects to understand the molecular bases of genetic correlations. A high density SNP map (5-20 SNP/cM) will be developed for the studied regions and genotyped across additional generations of BX animals to fine map QTL. Significant SNP markers developed from these approaches will be evaluated in additional commercially relevant lines of pig to ensure their applicability in commercial pigs. Markers that exhibit useful predictive genetic information will be disseminated to the swine industry. Finally with all of the genetic and phenotypic knowledge in hand, we should be well-equipped to determine the causative gene for some QTL and greatly improve our understanding of the physiological effects of these QTL. A precise location of the causative gene as predicted from fine mapping studies, knowledge about different biological pathways affected from the extensively phenotyped population and knowledge about the genes located in the region from the swine genome sequence should allow selection of positional candidate gene to study for causative variation. These studies will be supplemented with functional genomic and marker-assisted animal experimentation.
3. Progress Report
Due to a critical vacancy in personnel, we have not completed the QTL scans that were planned. However, significant progress has been made towards our stated objectives and some of the results obtained are in the process of being transferred to commercial swine production. While we were unable to conduct high density single nucleotide polymorphism (SNP) genotyping in quantitative trait loci (QTL) regions identified, we have conducted high density genotyping in the BX population (a Landrace-Duroc-Yorkshire composite population) for QTL regions identified in other populations. Targeted regions include QTL affecting pork palatability, female reproduction and sow longevity. Analyses of these targeted regions included fitting effects for intra-locus allelic interactions when possible. For pork quality, we have obtained approximately 1,500 samples from commercial pigs with detailed pork palatability data. These samples are being used in conjunction with our 1,200 sampled animals from previous studies to develop genetic markers for tenderness suitable for industry use. Our primary focus has been on measures of tenderness. These samples have been genotyped for approximately 100 SNP markers located in QTL regions. The most intriguing results are for markers within the calpastatin gene. These markers have been consistently associated with tenderness in all populations. Eighteen genes and a few other regions of the genome have been investigated for associations with female reproductive performance in over 1,000 BX sows. Markers were selected from regions previously reported to influence female reproduction with either genome scans or candidate gene approaches. Published markers along with novel markers were developed within previously reported genes and evaluated for significant associations with female reproductive performance. While genes involved in signaling or synthesis of reproductive hormones were frequently tested in the literature, our results indicate that genes affecting energy metabolism are also quite important, especially for rebreeding performance traits. In an attempt to conduct genome-wide association analyses, we collected data necessary to develop a high throughput SNP genotyping platform for commercial swine. A total of 115,572 markers were discovered and location in the swine genome determined. These markers were discovered by comparing over 5 million sequences with an average length of 232 bases. The sequences represented 421,060 segments of the pig genome. The location of each marker was predicted by comparing the segment to the sequence of the entire pig genome. The novel markers were combined with other publicly available markers to select the best set of markers for a commercial genotyping chip. These efforts resulted in approximately 60,000 genetic markers evenly spaced across the genome simultaneously assayed in a single reaction. After the genotyping platform was developed, in cooperation with Illumina, Inc. (see project report for 5438-31000-083-06S), we began genotyping 2,976 animals in the BX population with a broad range of phenotypic data for genome-wide association analyses.
1. Development of a high density SNP genotyping platform for commercial pigs. Technological advances have now made it possible to assay tens of thousands of genetic markers (single nucleotide polymorphisms or SNP) in a single reaction using a SNP chip. Before a commercially available SNP chip could be made, a sufficient number (approximately 500,000) of SNP markers were needed to ensure that the final chip contained useful markers evenly spaced across the genome. Scientists at USMARC contributed 115,572 novel SNP to combine with other publicly available markers and participated in SNP validation and chip design. Scientists at USMARC also contributed DNA samples for preliminary assessment of the SNP chip. The Illumina Porcine 60K SNP Chip was commercially released in February 2009 and is currently being used by many research labs and swine breeding companies around the world for genomic analyses in swine. This represents a significant advancement in genomic technologies for the swine industry.
2. Identification of predictive markers for pork tenderness. The identification of predictive DNA markers for pork quality would allow U.S. pork producers and breeders to more quickly and efficiently select genetically superior animals for production of consistent, high quality meat. Pork tenderness is a highly heritable trait and several chromosomal regions have been identified that are associated with differences in tenderness; one resides on chromosome 2 and contains the calpastatin gene. One hundred thirty genetic markers near the calpastatin gene were evaluated for association with instrumental shear force, an objective measure of pork tenderness. Five markers were identified that were consistently associated with shear force across four different populations of industry-relevant pigs. Two DNA sequence differences evaluated were associated with differences in the ability to bind nuclear proteins potentially altering calpastatin gene expression and were associated with differences in shear force. These SNPs are predictive of pork tenderness in industry populations and may be responsible for the differences in calpastatin gene expression which affects pork tenderness.
3. Determination of microRNA expression profiles during swine muscle development. MicroRNA, which are small non-coding RNA molecules, are known to play a key role in gene regulation. To evaluate the role of microRNA in skeletal muscle growth of the fetal pig, microRNAs were measured at three stages of gestation including: primary muscle fiber development (day 60), secondary muscle fiber development (day 90), and 10 days prior to birth (day 105). Adult muscle was also evaluated to compare muscle at a mature stage of growth to rapidly growing muscle. The relative abundance of approximately 40 microRNAs was determined in developing muscle tissue. In addition, 12 novel pig microRNA sequences were discovered. The knowledge of microRNAs present during muscle development provides clues to the regulation of muscle growth in swine, and will yield opportunities for improving pork production.
Kuehn, L.A., Nonneman, D.J., Klindt, J.M., Wise, T.H. 2009. Genetic relationships of body composition, serum leptin, and age at puberty in gilts. Journal of Animal Science. 87(2):477-483.