GenPhySE, Université de Toulouse, INRA, ENVT, 31326, Castanet-Tolosan, France.
INRA PEAT, 37380, Tours, France.
Genet Sel Evol. 2019 Apr 15;51(1):12. doi: 10.1186/s12711-019-0458-6.
In quail, two feather colour phenotypes i.e. fawn-2/beige and yellow are associated with the ASIP locus. The aim of our study was to characterize the structural modifications within this locus that explain the yellow mutation (large deletion) and the fawn-2/beige mutation (assumed to be caused by a different structural modification).
For the yellow phenotype, we identified a complex mutation that involves a 141,162-bp long deletion. For the fawn-2/beige phenotype, we identified a 71-kb tandem duplication that comprises one unchanged copy of ASIP and one copy present in the ITCH-ASIP fusion gene, which leads to a transcript coding for a normal ASIP protein. Although this agrees with previous reports that reported an increased level of ASIP transcripts in the skin of mutant animals, we show that in the skin from fawn-2/beige embryos, this level is higher than expected with a simple duplication of the ASIP gene. Thus, we hypothesize that the 5' region of the ITCH-ASIP fusion gene leads to a higher transcription level than the 5' region of the ASIP gene.
We were able to conclude that the fawn-2 and beige phenotypes are caused by the same allele at the ASIP locus. Both of the associated mutations fawn-2/beige and yellow lead to the formation of a fusion gene, which encodes a transcript for the ASIP protein. In both cases, transcription of ASIP depends on the promoter of a different gene, which includes alternative up-regulating sequences. However, we cannot exclude the possibility that the loss of the 5' region of the ASIP gene itself has additional impacts, especially for the fawn-2/beige mutation. In addition, in several other species including mammals, the existence of other dominant gain-of-function structural modifications that are localized upstream of the ASIP coding sequences has been reported, which supports our hypothesis that repressors in the 5' region of ASIP are absent in the fawn-2/beige mutant.
在鹌鹑中,两种羽毛颜色表型即 fawn-2/beige 和 yellow 与 ASIP 基因座相关。我们研究的目的是描述解释黄色突变(大片段缺失)和 fawn-2/beige 突变(假定由不同的结构修饰引起)的该基因座内的结构修饰。
对于黄色表型,我们鉴定出涉及 141162bp 长缺失的复杂突变。对于 fawn-2/beige 表型,我们鉴定出一个 71kb 的串联重复,其中包含一个未改变的 ASIP 拷贝和一个位于 ITCH-ASIP 融合基因中的拷贝,导致编码正常 ASIP 蛋白的转录本。虽然这与先前报道的在突变动物皮肤中 ASIP 转录本水平增加的报道一致,但我们表明在 fawn-2/beige 胚胎的皮肤中,该水平高于预期的 ASIP 基因简单重复。因此,我们假设 ITCH-ASIP 融合基因的 5' 区域导致比 ASIP 基因的 5' 区域更高的转录水平。
我们能够得出结论,fawn-2 和 beige 表型是由 ASIP 基因座上的相同等位基因引起的。两种相关的突变 fawn-2/beige 和 yellow 均导致融合基因的形成,该融合基因编码 ASIP 蛋白的转录本。在这两种情况下,ASIP 的转录均依赖于不同基因的启动子,其中包含替代的上调序列。然而,我们不能排除 ASIP 基因本身的 5' 区域丢失可能会有其他影响的可能性,尤其是对于 fawn-2/beige 突变。此外,在包括哺乳动物在内的其他几种物种中,已经报道了其他位于 ASIP 编码序列上游的显性获得性功能结构修饰的存在,这支持我们的假设,即 fawn-2/beige 突变体中不存在 ASIP 5' 区域的抑制物。