Association analyses of candidate single nucleotide polymorphisms on reproductive traits in swine
The ability to identify young females with superior reproduction would have a large economic impact on commercial swine production. Previous studies have discovered SNP associated with economically important traits such as litter size, growth rate, and feed intake. The objective of this study was to...
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description | The ability to identify young females with superior reproduction would have a large economic impact on commercial swine production. Previous studies have discovered SNP associated with economically important traits such as litter size, growth rate, and feed intake. The objective of this study was to test for association of candidate SNP with sow prolificacy reproductive traits in gilts of a Landrace-Duroc-Yorkshire composite population. Association analyses regressed additive (A), dominant (D), and imprinting (I) SNP effects on each trait with an animal model. A carnitine palmitoyltransferase 1A SNP and a glycogen synthase 1 SNP were associated with age at puberty (AP; D = 10 d; P = 0. 0037 and A = 3.8 d; P = 0.0078, respectively). Four IGF2 SNP were associated with AP as well, having additive or dominant effects (3.2 to 5.8 d; P [less-than or equal to] 0.0052). Two mannosidase 2B2 SNP and 2 prolactin receptor (PRLR) SNP were also associated with AP. Solute carrier 22, subfamily member 5 SNP was weakly associated with AP (D = 3.9 d; P < 0.10). Polymorphisms within glycogen synthase 1 and protein kinase AMP-activated, gamma 3 noncatalytic subunit had associations with ovulation rate. Estrogen receptor (ESR) 1, ESR2, PPAR γ coactivator 1, and IGFBP3 SNP were significantly associated with weaning-to-estrus interval. Two PRLR SNP were associated with total number of piglets born (A = 0.57 piglets; P = 0.0095 and D = 0.61 piglets; P = 0.0016, respectively). A SNP within PRLR was also associated with number of piglets born alive (D = 0.61; P = 0.0016). The PPAR γ coactivator 1 SNP was associated with total number of piglets born (D = 0.38 piglets; P = 0.0391) and number of piglets born alive (D = 0.53 piglets; P = 0.0032). The SNP within ESR1 (A = 0.65 piglets; P = 0.0950), ESR2 (A = -0.33 piglets; P = 0.0176), IGF2 SNP (A = -0.26 piglets; P = 0.0032), and IGFBP3 SNP (D = 0.35 piglets; P = 0.0683) were associated with number of piglets born dead. A leptin SNP was associated with mummified fetuses (D = 0.09 piglets; P = 0.0978). Many of the SNP analyzed in this study are from genes involved in regulation of metabolism, suggesting that there is an important link between physiological events associated with reproduction and energy utilization. Furthermore, these production and growth trait SNP may serve to assist in selection of young females for superior reproductive performance. |
doi_str_mv | 10.2527/jas.2009-1985 |
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Previous studies have discovered SNP associated with economically important traits such as litter size, growth rate, and feed intake. The objective of this study was to test for association of candidate SNP with sow prolificacy reproductive traits in gilts of a Landrace-Duroc-Yorkshire composite population. Association analyses regressed additive (A), dominant (D), and imprinting (I) SNP effects on each trait with an animal model. A carnitine palmitoyltransferase 1A SNP and a glycogen synthase 1 SNP were associated with age at puberty (AP; D = 10 d; P = 0. 0037 and A = 3.8 d; P = 0.0078, respectively). Four IGF2 SNP were associated with AP as well, having additive or dominant effects (3.2 to 5.8 d; P [less-than or equal to] 0.0052). Two mannosidase 2B2 SNP and 2 prolactin receptor (PRLR) SNP were also associated with AP. Solute carrier 22, subfamily member 5 SNP was weakly associated with AP (D = 3.9 d; P < 0.10). Polymorphisms within glycogen synthase 1 and protein kinase AMP-activated, gamma 3 noncatalytic subunit had associations with ovulation rate. Estrogen receptor (ESR) 1, ESR2, PPAR γ coactivator 1, and IGFBP3 SNP were significantly associated with weaning-to-estrus interval. Two PRLR SNP were associated with total number of piglets born (A = 0.57 piglets; P = 0.0095 and D = 0.61 piglets; P = 0.0016, respectively). A SNP within PRLR was also associated with number of piglets born alive (D = 0.61; P = 0.0016). The PPAR γ coactivator 1 SNP was associated with total number of piglets born (D = 0.38 piglets; P = 0.0391) and number of piglets born alive (D = 0.53 piglets; P = 0.0032). The SNP within ESR1 (A = 0.65 piglets; P = 0.0950), ESR2 (A = -0.33 piglets; P = 0.0176), IGF2 SNP (A = -0.26 piglets; P = 0.0032), and IGFBP3 SNP (D = 0.35 piglets; P = 0.0683) were associated with number of piglets born dead. A leptin SNP was associated with mummified fetuses (D = 0.09 piglets; P = 0.0978). Many of the SNP analyzed in this study are from genes involved in regulation of metabolism, suggesting that there is an important link between physiological events associated with reproduction and energy utilization. Furthermore, these production and growth trait SNP may serve to assist in selection of young females for superior reproductive performance.</description><identifier>ISSN: 0021-8812</identifier><identifier>EISSN: 1525-3163</identifier><identifier>DOI: 10.2527/jas.2009-1985</identifier><identifier>PMID: 19749016</identifier><language>eng</language><publisher>Champaign, IL: American Society of Animal Science</publisher><subject>additive gene effects ; Animal productions ; animal proteins ; animal reproduction ; Animals ; Biological and medical sciences ; DNA ; dominance (genetics) ; energy metabolism ; fecundity ; feed intake ; Female ; female fertility ; fetal death ; fetus ; Fundamental and applied biological sciences. Psychology ; genes ; genetic variation ; genomic imprinting ; Genotype ; Litter Size ; Male ; Odds Ratio ; Ovulation ; Parity ; piglets ; Polymorphism, Single Nucleotide ; Pregnancy ; Reproduction - genetics ; Sexual Maturation ; single nucleotide polymorphism ; sows ; swine ; Swine - genetics ; Swine - physiology ; Terrestrial animal productions ; Vertebrates</subject><ispartof>Journal of animal science, 2010, Vol.88 (1), p.1-15</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22332437$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19749016$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rempel, L.A</creatorcontrib><creatorcontrib>Nonneman, D.J</creatorcontrib><creatorcontrib>Wise, T.H</creatorcontrib><creatorcontrib>Erkens, T</creatorcontrib><creatorcontrib>Peelman, L.J</creatorcontrib><creatorcontrib>Rohrer, G.A</creatorcontrib><title>Association analyses of candidate single nucleotide polymorphisms on reproductive traits in swine</title><title>Journal of animal science</title><addtitle>J Anim Sci</addtitle><description>The ability to identify young females with superior reproduction would have a large economic impact on commercial swine production. Previous studies have discovered SNP associated with economically important traits such as litter size, growth rate, and feed intake. The objective of this study was to test for association of candidate SNP with sow prolificacy reproductive traits in gilts of a Landrace-Duroc-Yorkshire composite population. Association analyses regressed additive (A), dominant (D), and imprinting (I) SNP effects on each trait with an animal model. A carnitine palmitoyltransferase 1A SNP and a glycogen synthase 1 SNP were associated with age at puberty (AP; D = 10 d; P = 0. 0037 and A = 3.8 d; P = 0.0078, respectively). Four IGF2 SNP were associated with AP as well, having additive or dominant effects (3.2 to 5.8 d; P [less-than or equal to] 0.0052). Two mannosidase 2B2 SNP and 2 prolactin receptor (PRLR) SNP were also associated with AP. Solute carrier 22, subfamily member 5 SNP was weakly associated with AP (D = 3.9 d; P < 0.10). Polymorphisms within glycogen synthase 1 and protein kinase AMP-activated, gamma 3 noncatalytic subunit had associations with ovulation rate. Estrogen receptor (ESR) 1, ESR2, PPAR γ coactivator 1, and IGFBP3 SNP were significantly associated with weaning-to-estrus interval. Two PRLR SNP were associated with total number of piglets born (A = 0.57 piglets; P = 0.0095 and D = 0.61 piglets; P = 0.0016, respectively). A SNP within PRLR was also associated with number of piglets born alive (D = 0.61; P = 0.0016). The PPAR γ coactivator 1 SNP was associated with total number of piglets born (D = 0.38 piglets; P = 0.0391) and number of piglets born alive (D = 0.53 piglets; P = 0.0032). The SNP within ESR1 (A = 0.65 piglets; P = 0.0950), ESR2 (A = -0.33 piglets; P = 0.0176), IGF2 SNP (A = -0.26 piglets; P = 0.0032), and IGFBP3 SNP (D = 0.35 piglets; P = 0.0683) were associated with number of piglets born dead. A leptin SNP was associated with mummified fetuses (D = 0.09 piglets; P = 0.0978). Many of the SNP analyzed in this study are from genes involved in regulation of metabolism, suggesting that there is an important link between physiological events associated with reproduction and energy utilization. Furthermore, these production and growth trait SNP may serve to assist in selection of young females for superior reproductive performance.</description><subject>additive gene effects</subject><subject>Animal productions</subject><subject>animal proteins</subject><subject>animal reproduction</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>DNA</subject><subject>dominance (genetics)</subject><subject>energy metabolism</subject><subject>fecundity</subject><subject>feed intake</subject><subject>Female</subject><subject>female fertility</subject><subject>fetal death</subject><subject>fetus</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>genes</subject><subject>genetic variation</subject><subject>genomic imprinting</subject><subject>Genotype</subject><subject>Litter Size</subject><subject>Male</subject><subject>Odds Ratio</subject><subject>Ovulation</subject><subject>Parity</subject><subject>piglets</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Pregnancy</subject><subject>Reproduction - genetics</subject><subject>Sexual Maturation</subject><subject>single nucleotide polymorphism</subject><subject>sows</subject><subject>swine</subject><subject>Swine - genetics</subject><subject>Swine - physiology</subject><subject>Terrestrial animal productions</subject><subject>Vertebrates</subject><issn>0021-8812</issn><issn>1525-3163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo90c9rFDEUB_Agit1Wj141IOJpan5sJpljKVqFggftObzJvOymZJI1mWnZ_97Arp7e5cOX73uPkHecXQsl9JdHqNeCsaHjg1EvyIYroTrJe_mSbBgTvDOGiwtyWesjY1yoQb0mF3zQ24HxfkPgptbsAiwhJwoJ4rFipdlTB2kKEyxIa0i7iDStLmJewoT0kONxzuWwD3VuONGCh5Kn1S3hCelSICyVhkTrc0j4hrzyECu-Pc8r8vDt6-_b7939z7sftzf3nReDWDocFXdGSbOFUSmQjvWKTd57LQ0KiWbUrveC4TT2gEIAU1q0FXjbGwyM8op8PuW2Kn9WrIudQ3UYIyTMa7Vayp6ZLVNNvj_LdZxxsocSZihH--8qDXw6A6gOoi-QXKj_nRBSiq3UzX08uX3Y7Z9DQVtniLHFctv-Yozlljf14aQ8ZAu70pIefrXqknHNtRik_AuokohM</recordid><startdate>2010</startdate><enddate>2010</enddate><creator>Rempel, L.A</creator><creator>Nonneman, D.J</creator><creator>Wise, T.H</creator><creator>Erkens, T</creator><creator>Peelman, L.J</creator><creator>Rohrer, G.A</creator><general>American Society of Animal Science</general><general>Am Soc Animal Sci</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>2010</creationdate><title>Association analyses of candidate single nucleotide polymorphisms on reproductive traits in swine</title><author>Rempel, L.A ; Nonneman, D.J ; Wise, T.H ; Erkens, T ; Peelman, L.J ; Rohrer, G.A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f292t-eb51c85384ab55a3c0650dfff738e23e8b7c6f20edb6ae22a05720161198a8ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>additive gene effects</topic><topic>Animal productions</topic><topic>animal proteins</topic><topic>animal reproduction</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>DNA</topic><topic>dominance (genetics)</topic><topic>energy metabolism</topic><topic>fecundity</topic><topic>feed intake</topic><topic>Female</topic><topic>female fertility</topic><topic>fetal death</topic><topic>fetus</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>genes</topic><topic>genetic variation</topic><topic>genomic imprinting</topic><topic>Genotype</topic><topic>Litter Size</topic><topic>Male</topic><topic>Odds Ratio</topic><topic>Ovulation</topic><topic>Parity</topic><topic>piglets</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Pregnancy</topic><topic>Reproduction - genetics</topic><topic>Sexual Maturation</topic><topic>single nucleotide polymorphism</topic><topic>sows</topic><topic>swine</topic><topic>Swine - genetics</topic><topic>Swine - physiology</topic><topic>Terrestrial animal productions</topic><topic>Vertebrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rempel, L.A</creatorcontrib><creatorcontrib>Nonneman, D.J</creatorcontrib><creatorcontrib>Wise, T.H</creatorcontrib><creatorcontrib>Erkens, T</creatorcontrib><creatorcontrib>Peelman, L.J</creatorcontrib><creatorcontrib>Rohrer, G.A</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of animal science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rempel, L.A</au><au>Nonneman, D.J</au><au>Wise, T.H</au><au>Erkens, T</au><au>Peelman, L.J</au><au>Rohrer, G.A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association analyses of candidate single nucleotide polymorphisms on reproductive traits in swine</atitle><jtitle>Journal of animal science</jtitle><addtitle>J Anim Sci</addtitle><date>2010</date><risdate>2010</risdate><volume>88</volume><issue>1</issue><spage>1</spage><epage>15</epage><pages>1-15</pages><issn>0021-8812</issn><eissn>1525-3163</eissn><abstract>The ability to identify young females with superior reproduction would have a large economic impact on commercial swine production. Previous studies have discovered SNP associated with economically important traits such as litter size, growth rate, and feed intake. The objective of this study was to test for association of candidate SNP with sow prolificacy reproductive traits in gilts of a Landrace-Duroc-Yorkshire composite population. Association analyses regressed additive (A), dominant (D), and imprinting (I) SNP effects on each trait with an animal model. A carnitine palmitoyltransferase 1A SNP and a glycogen synthase 1 SNP were associated with age at puberty (AP; D = 10 d; P = 0. 0037 and A = 3.8 d; P = 0.0078, respectively). Four IGF2 SNP were associated with AP as well, having additive or dominant effects (3.2 to 5.8 d; P [less-than or equal to] 0.0052). Two mannosidase 2B2 SNP and 2 prolactin receptor (PRLR) SNP were also associated with AP. Solute carrier 22, subfamily member 5 SNP was weakly associated with AP (D = 3.9 d; P < 0.10). Polymorphisms within glycogen synthase 1 and protein kinase AMP-activated, gamma 3 noncatalytic subunit had associations with ovulation rate. Estrogen receptor (ESR) 1, ESR2, PPAR γ coactivator 1, and IGFBP3 SNP were significantly associated with weaning-to-estrus interval. Two PRLR SNP were associated with total number of piglets born (A = 0.57 piglets; P = 0.0095 and D = 0.61 piglets; P = 0.0016, respectively). A SNP within PRLR was also associated with number of piglets born alive (D = 0.61; P = 0.0016). The PPAR γ coactivator 1 SNP was associated with total number of piglets born (D = 0.38 piglets; P = 0.0391) and number of piglets born alive (D = 0.53 piglets; P = 0.0032). The SNP within ESR1 (A = 0.65 piglets; P = 0.0950), ESR2 (A = -0.33 piglets; P = 0.0176), IGF2 SNP (A = -0.26 piglets; P = 0.0032), and IGFBP3 SNP (D = 0.35 piglets; P = 0.0683) were associated with number of piglets born dead. A leptin SNP was associated with mummified fetuses (D = 0.09 piglets; P = 0.0978). Many of the SNP analyzed in this study are from genes involved in regulation of metabolism, suggesting that there is an important link between physiological events associated with reproduction and energy utilization. Furthermore, these production and growth trait SNP may serve to assist in selection of young females for superior reproductive performance.</abstract><cop>Champaign, IL</cop><pub>American Society of Animal Science</pub><pmid>19749016</pmid><doi>10.2527/jas.2009-1985</doi><tpages>15</tpages></addata></record> |
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subjects | additive gene effects Animal productions animal proteins animal reproduction Animals Biological and medical sciences DNA dominance (genetics) energy metabolism fecundity feed intake Female female fertility fetal death fetus Fundamental and applied biological sciences. Psychology genes genetic variation genomic imprinting Genotype Litter Size Male Odds Ratio Ovulation Parity piglets Polymorphism, Single Nucleotide Pregnancy Reproduction - genetics Sexual Maturation single nucleotide polymorphism sows swine Swine - genetics Swine - physiology Terrestrial animal productions Vertebrates |
title | Association analyses of candidate single nucleotide polymorphisms on reproductive traits in swine |
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