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候选基因Clock定位于虹鳟鱼一个强大的产卵时间数量性状基因座区域。

The candidate gene, Clock, localizes to a strong spawning time quantitative trait locus region in rainbow trout.

作者信息

Leder E H, Danzmann R G, Ferguson M M

机构信息

Department of Integrative Biology, University of Guelph, Guelph, Ontario, Canada N1G 2W1.

出版信息

J Hered. 2006 Jan-Feb;97(1):74-80. doi: 10.1093/jhered/esj004. Epub 2006 Jan 11.

Abstract

We applied a candidate gene mapping approach to an existing quantitative trait loci (QTL) data set for spawning date in rainbow trout (Oncorynchus mykiss) to ascertain whether these genes could potentially account for any observed QTL effects. Several genes were chosen for their known or suspected roles in reproduction, circadian, or circannual timing, including salmon-type gonadotropin-releasing hormone 3A and 3B (GnRH3A and GnRH3B), Clock, Period1, and arylalkylamine N-acetlytransferase-1 and -2 (AANAT-1 and AANAT-2). Genes were sequenced, and polymorphisms were identified in parents of two rainbow trout mapping families, one of which was used previously to detect spawn timing QTL. Interval mapping was used to identify associations between genetic markers and spawning date effects. Using a genetic map that was updated with 574 genetic markers (775 total), we found evidence for 11 significant or suggestive QTL regions. Most QTL were only localized within one of the parents; however, a strong QTL region was identified in both female and male parents on linkage group RT-8 that explained 20% and 50% of trait variance, respectively. The Clock gene mapped to this region. Period1 mapped to a region in the female parent associated with a marginal effect (P = .056) on spawn timing. Other candidate genes were not associated with significant QTL effects.

摘要

我们将候选基因定位方法应用于现有的虹鳟(Oncorynchus mykiss)产卵日期数量性状基因座(QTL)数据集,以确定这些基因是否可能解释任何观察到的QTL效应。选择了几个在生殖、昼夜节律或年节律定时方面具有已知或疑似作用的基因,包括鲑鱼型促性腺激素释放激素3A和3B(GnRH3A和GnRH3B)、Clock、Period1以及芳基烷基胺N - 乙酰基转移酶 - 1和 - 2(AANAT - 1和AANAT - 2)。对基因进行了测序,并在两个虹鳟作图家系的亲本中鉴定出多态性,其中一个家系先前已用于检测产卵时间QTL。区间作图用于识别遗传标记与产卵日期效应之间的关联。使用一个更新后包含574个遗传标记(共775个)的遗传图谱,我们发现了11个显著或提示性QTL区域的证据。大多数QTL仅定位在一个亲本中;然而,在连锁群RT - 8的雌性和雄性亲本中都鉴定出一个强QTL区域,分别解释了性状变异的20%和50%。Clock基因定位到该区域。Period1定位到雌性亲本中与产卵时间的边缘效应(P = 0.056)相关的一个区域。其他候选基因与显著的QTL效应无关。

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