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小鼠刺鼠毛色基因座的分子标记

Molecular markers for the agouti coat color locus of the mouse.

作者信息

Lovett M, Cheng Z Y, Lamela E M, Yokoi T, Epstein C J

出版信息

Genetics. 1987 Apr;115(4):747-54. doi: 10.1093/genetics/115.4.747.

Abstract

The agouti (a) coat color locus of the mouse acts within the microenvironment of the hair follicle to control the relative amount and distribution of yellow and black pigment in the coat hairs. Over 18 different mutations with complex dominance relationships have been described at this locus. The lethal yellow (Ay) mutation is the top dominant of this series and is uniquely associated with an endogenous provirus, Emv-15, in three highly inbred strains. However, we report here that it is unlikely that the provirus itself causes the Ay-associated alteration in coat color, since one strain of mice (YBR-Ay/a) lacks the provirus but still retains a yellow coat color. Using single-copy mouse DNA sequences from the regions flanking Emv-15 we have detected three patterns of restriction fragment length polymorphisms (RFLPs) within this region that can be used as molecular markers for different agouti locus alleles: a wild-type agouti (A) pattern, a pattern which generally cosegregates with the nonagouti (a) mutation, and a pattern which is specific to Emv-15. We have used these RFLPs and a panel of 28 recombinant inbred mouse strains to determine the genetic linkage of these sequences with the agouti locus and have found complete concordance between the two (95% confidence limit of 0.00 to 3.79 centimorgans). We have also physically mapped these sequences by in situ hybridization to band H1 of chromosome 2, thus directly confirming previous assignments of the location of the agouti locus.

摘要

小鼠的刺鼠(a)毛色位点在毛囊的微环境中起作用,以控制被毛中黄色和黑色色素的相对含量及分布。该位点已发现超过18种具有复杂显性关系的不同突变。致死黄色(Ay)突变是该系列中最显性的突变,并且在三个高度近交系中与内源性前病毒Emv - 15独特相关。然而,我们在此报告,前病毒本身不太可能导致与Ay相关的毛色改变,因为一种小鼠品系(YBR - Ay/a)缺乏该前病毒,但仍保留黄色被毛。利用Emv - 15侧翼区域的单拷贝小鼠DNA序列,我们在该区域检测到三种限制性片段长度多态性(RFLP)模式,可作为不同刺鼠位点等位基因的分子标记:野生型刺鼠(A)模式、通常与非刺鼠(a)突变共分离的模式以及Emv - 15特有的模式。我们利用这些RFLP和一组28个重组近交小鼠品系来确定这些序列与刺鼠位点的遗传连锁关系,发现两者完全一致(9

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