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初级性别决定机制的关键方面在果蝇属中是保守的。

Key aspects of the primary sex determination mechanism are conserved across the genus Drosophila.

作者信息

Erickson J W, Cline T W

机构信息

Department of Molecular and Cell Biology, Division of Genetics, University of California, Berkeley, CA 94720-3204, USA.

出版信息

Development. 1998 Aug;125(16):3259-68. doi: 10.1242/dev.125.16.3259.

Abstract

In D. melanogaster, a set of 'X:A numerator genes', which includes sisterlessA (sisA), determines sex by controlling the transcription of Sex-lethal (Sxl). We characterized sisA from D. pseudoobscura and D. virilis and studied the timing of sisA and Sxl expression with single cell-cycle resolution in D. virilis, both to guide structure-function studies of sisA and to help understand sex determination evolution. We found that D. virilis sisA shares 58% amino acid identity with its melanogaster ortholog. The identities confirm sisA as an atypical bZIP transcription factor. Although virilis sisA can substitute for melanogaster sisA, the protein is not fully functional in a heterologous context. The putative sisA regulatory sequence CAGGTAG is a potential 'numerator box,' since it is shared with the other strong X:A numerator gene, sisB, and its target, SxlPe. Temporal and spatial features of sisA and SxlPe expression are strikingly conserved, including rapid onset and cessation of transcription in somatic nuclei, early cessation of sisA transcription in budding pole cells and persistent high-level sisA expression in yolk nuclei. Expression of sisA and Sxl is as tightly coupled in virilis as it is in melanogaster. Taken together, these data indicate that the same primary sex determination mechanism exists throughout the genus Drosophila.

摘要

在黑腹果蝇中,一组“X:A 分子基因”,包括无姐妹 A(sisA),通过控制性致死基因(Sxl)的转录来决定性别。我们对拟暗果蝇和粗壮果蝇的 sisA 进行了表征,并在粗壮果蝇中以单细胞周期分辨率研究了 sisA 和 Sxl 的表达时间,这既有助于指导 sisA 的结构功能研究,也有助于理解性别决定的进化。我们发现粗壮果蝇的 sisA 与其黑腹果蝇直系同源基因具有 58%的氨基酸同一性。这些同一性证实 sisA 是一种非典型的 bZIP 转录因子。虽然粗壮果蝇的 sisA 可以替代黑腹果蝇的 sisA,但该蛋白在异源环境中并不完全功能正常。推测的 sisA 调控序列 CAGGTAG 是一个潜在的“分子框”,因为它与另一个强大的 X:A 分子基因 sisB 及其靶标 SxlPe 共享。sisA 和 SxlPe 表达的时间和空间特征显著保守,包括体细胞核中转录的快速起始和终止、出芽极细胞中 sisA 转录的早期终止以及卵黄核中 sisA 的持续高水平表达。sisA 和 Sxl 的表达在粗壮果蝇中与在黑腹果蝇中一样紧密耦合。综上所述,这些数据表明整个果蝇属存在相同的初级性别决定机制。

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