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果蝇双胸复合体的分子遗传学:腹部B区的顺式调控

The molecular genetics of the bithorax complex of Drosophila: cis-regulation in the Abdominal-B domain.

作者信息

Celniker S E, Sharma S, Keelan D J, Lewis E B

机构信息

Division of Biology, California Institute of Technology, Pasadena 91125.

出版信息

EMBO J. 1990 Dec;9(13):4277-86. doi: 10.1002/j.1460-2075.1990.tb07876.x.

Abstract

In Drosophila the Abdominal-B (Abd-B) domain of the bithorax complex (BX-C) spans over 100 kb and is responsible for specifying the identities of adult abdominal segments five (A5) to nine (A9), inclusive, and correspondingly, neuromeres 10-14 of the embryonic central nervous system. The domain consists of a region coding for two proteins, ABD-BI (54 kd) and ABD-BII (36 kd) and cis-regulatory regions extending from infra-abdominal-5 (iab-5) to iab-9, inclusive. We have used a monoclonal anti-ABD-B antibody to infer that mutants in iab-8 eliminate the expression of ABD-BI in neuromeres 10-13, inclusive, and that mutants in iab-9 eliminate expression of ABD-BII in neuromere 14. ABD-B expression is also analyzed in homozygotes for (i) loss-of-function mutants involving the iab-5, iab-6 and iab-7 regions, (ii) gain-of-function mutants Miscadastral pigmentation (Mcp) and Superabdominal (Sab), and (iii) a trans-regulator, Polycomb (Pc). ABD-B expression along the antero-posterior axis is colinear with the chromosomal order of the cis-regulatory regions. The behavior of rearrangement-associated iab-6 and iab-7 mutants suggests that the enhancer-like region, iab-5, and possibly also iab-6, may be shared between the abd-A and Abd-B domains. Such sharing is proposed as a factor that tends to keep gene complexes intact during evolution.

摘要

在果蝇中,双胸复合体(BX-C)的腹部B(Abd-B)结构域跨度超过100 kb,负责指定成年腹部第5节(A5)至第9节(A9)(包括第5节和第9节)的身份,相应地,也负责指定胚胎中枢神经系统神经节10 - 14的身份。该结构域由一个编码两种蛋白质的区域组成,即ABD-BI(54 kd)和ABD-BII(36 kd),以及从腹下-5(iab-5)延伸至iab-9(包括iab-5和iab-9)的顺式调控区域。我们使用一种抗ABD-B单克隆抗体推断,iab-8中的突变会消除神经节10至13(包括神经节10和神经节13)中ABD-BI的表达,而iab-9中的突变会消除神经节14中ABD-BII的表达。还在以下纯合子中分析了ABD-B的表达:(i)涉及iab-5、iab-6和iab-7区域的功能丧失突变体;(ii)功能获得突变体杂散色素沉着(Mcp)和超腹部(Sab);(iii)一种反式调节因子多梳蛋白(Pc)。沿前后轴的ABD-B表达与顺式调控区域的染色体顺序共线性。与重排相关的iab-6和iab-7突变体的行为表明,增强子样区域iab-5,可能还有iab-6,可能在abd-A和Abd-B结构域之间共享。这种共享被认为是在进化过程中倾向于保持基因复合体完整的一个因素。

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