Muñoz Gloria, Ovilo Cristina, Estellé Jordi, Silió Luis, Fernández Almudena, Rodriguez Carmen
Departamento de Mejora Genética Animal, SGIT-INIA, 28040 Madrid, Spain.
Genet Sel Evol. 2007 Mar-Apr;39(2):195-206. doi: 10.1186/1297-9686-39-2-195. Epub 2007 Feb 17.
The objective of this study was to search for polymorphisms in the coding region of the estrogen receptors 1 and 2 (ESR1 and ESR2) and to analyze the effects of these variants and the well known intronic ESR1 PvuII polymorphism on litter size in a Chinese-European pig line. We identified five silent single nucleotide polymorphisms (SNP) in the ESR1 cDNA: c.669T > C (exon 3), c.1227C > T (exon 5), c.1452C > T (exon 7), c.1665T > C and c.1755A > G (exon 8). One pair of these SNP (c.1665T > C and c.1755A > G) co-segregated in the analyzed line, and the SNP c.669T > C showed the same segregation pattern as the PvuII polymorphism. These polymorphisms were tested in this study, although the c.1452C > T SNP within exon 7 was not analyzed due to its low informativeness. In the ESR2 cDNA, one missense SNP was found within exon 5, which caused an amino acid substitution in the coded protein: "c.949G > A (p.Val317Met)" and was tested on sow litter size. Information on 1622 litter records from 408 genotyped sows was analyzed to determine whether these SNP influenced the total number of piglets born (TNB) or the number of born alive (NBA). The polymorphisms ESR1: [ PvuII; c.669T > C] , ESR1: [ c.1665T > C; c.1755A > G] and ESR2: c.949G > A showed no statistically significant association with litter size. However, the ESR1: c.1227T allele was significantly associated with TNB. The additive substitution effect was estimated to be 0.40 piglets born per litter (P < 0.03), and no dominance effects were observed. This SNP could be useful in assisted selection for litter size in some pig lines, as a new genetic marker in linkage disequilibrium with the causative mutation.
本研究的目的是寻找雌激素受体1和2(ESR1和ESR2)编码区的多态性,并分析这些变异以及著名的ESR1内含子PvuII多态性对中欧猪系产仔数的影响。我们在ESR1 cDNA中鉴定出五个沉默单核苷酸多态性(SNP):c.669T>C(外显子3)、c.1227C>T(外显子5)、c.1452C>T(外显子7)、c.1665T>C和c.1755A>G(外显子8)。其中一对SNP(c.1665T>C和c.1755A>G)在分析的猪系中共同分离,SNP c.669T>C显示出与PvuII多态性相同的分离模式。尽管外显子7中的c.1452C>T SNP因信息性低未进行分析,但本研究对这些多态性进行了检测。在ESR2 cDNA中,在外显子5内发现一个错义SNP,导致编码蛋白中的氨基酸替换:“c.949G>A(p.Val317Met)”,并对母猪产仔数进行了检测。分析了来自408头基因分型母猪的1622窝产仔记录信息,以确定这些SNP是否影响产仔总数(TNB)或存活仔猪数(NBA)。ESR1多态性:[PvuII;c.669T>C]、ESR1:[c.1665T>C;c.1755A>G]和ESR2:c.949G>A与产仔数无统计学显著关联。然而,ESR1:c.1227T等位基因与TNB显著相关。估计加性替换效应为每窝产仔0.40头仔猪(P<0.03),未观察到显性效应。作为与致病突变处于连锁不平衡状态的新遗传标记,该SNP在某些猪系的产仔数辅助选择中可能有用。