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BTA7 上生育力 QTL 的精细定位及其与以色列荷斯坦牛中 CNV 的关联。

Fine Mapping of a QTL for Fertility on BTA7 and Its Association With a CNV in the Israeli Holsteins.

出版信息

G3 (Bethesda). 2011 Jun;1(1):65-74. doi: 10.1534/g3.111.000299. Epub 2011 Jun 1.

Abstract

A quantitative trait locus (QTL) affecting female fertility, scored as the inverse of the number of inseminations to conception, on Bos taurus chromosome 7 was detected by a daughter design analysis of the Israeli Holstein population (P < 0.0003). Sires of five of the 10 families analyzed were heterozygous for the QTL. The 95% confidence interval of the QTL spans 27 cM from the centromere. Seven hundred and four SNP markers on the Illumina BovineSNP50 BeadChip within the QTL confidence interval were tested for concordance. A single SNP, NGS-58779, was heterozygous for all the five QTL heterozygous patriarchs, and homozygous for the remaining five QTL homozygous sires. A significant effect on fertility was associated with this marker in the sample of 900 sires genotyped (P < 10(-6)). Haplotype phase was the same for four of the five segregating sires. Thus concordance was obtained in nine of the ten families. We identified a common haplotype region associated with the rare and economically favorable allele of the SNP, spanning 270 kbp on BTA7 upstream to 4.72 Mbp. Eleven genes found in the common haplotype region should be considered as positional candidates for the identification of the causative quantitative trait nucleotide. Copy number variation was found in one of these genes, KIAA1683. Four gene variants were identified, but only the number of copies of a specific variant (V(1)) was significantly associated with breeding values of sires for fertility.

摘要

一个影响雌性生育力的数量性状基因座(QTL),以授精次数的倒数来衡量,通过对以色列荷斯坦牛群体的女儿设计分析检测到(P<0.0003)。在分析的 10 个家系中,有 5 个家系的雄性为该 QTL 的杂合子。QTL 的 95%置信区间跨越着丝粒的 27cM。在 QTL 置信区间内的 Illumina BovineSNP50 BeadChip 上的 704 个 SNP 标记用于检测一致性。一个 SNP,NGS-58779,在所有 5 个 QTL 杂合子雄性中都是杂合子,而在其余 5 个 QTL 纯合子雄性中是纯合子。在 900 个已测交雄性样本中,该标记与生育力显著相关(P<10(-6))。在 5 个分离雄性中,有 4 个的单倍型相位相同。因此,在 10 个家系中有 9 个获得了一致性。我们确定了一个与 SNP 稀有和经济有利等位基因相关的常见单倍型区域,跨越 BTA7 上游的 270kbp 到 4.72Mbp。在常见单倍型区域中发现的 11 个基因应被视为鉴定引起数量性状核苷酸的候选基因。在其中一个基因 KIAA1683 中发现了拷贝数变异。鉴定出 4 个基因变体,但只有特定变体(V(1))的拷贝数与雄性的繁殖值与生育力显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d2/3276122/8db02186e2a9/65f1.jpg

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