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肿瘤头-1基因座影响黑腹果蝇表皮的刚毛数量。

The tumorous-head-1 locus affects bristle number of the Drosophila melanogaster cuticle.

作者信息

Packert G, Kuhn D T

机构信息

Department of Biology, University of Central Florida, Orlando 32816-0990, USA.

出版信息

Genetics. 1998 Feb;148(2):743-52. doi: 10.1093/genetics/148.2.743.

DOI:10.1093/genetics/148.2.743
PMID:9504921
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1459811/
Abstract

The tuh-1 maternal effect locus contains two naturally occurring isoalleles, tuh-1h and tuh-1g. Until recently there has been no possibility to distinguish between the tuh-lh and the tuh-1g maternal effects other than evaluating their effect on the Bithorax-Complex (BXC) Abdominal B (Abd-B) mutant tuh-3. However, in this report we identify a bristle phenotype associated with the tuh-1 locus that has very interesting evolutionary implications. Females homozygous for tuh-1h always produce adult offspring with more bristles than females homozygous or heterozygous for tuh-1g. The effect is global. Increased bristle number occurs in the head, the thorax, and the anterior and posterior abdomen. Females totally deficient for the tuh-1 gene produce offspring with high bristle number. Thus, the bristle phenotype results from the absence of the maternally contributed tuh-1g factor. Genetic evidence shows that the bristle phenotype is caused by the tuh-1 locus and that tuh-1h is completely recessive to tuh-1g. The tuh-1 locus is located at the euchromatin-beta-heterochromatin junction near the centromere of the X chromosome and deficiency analysis places the locus between the lethal genes extra organs (eo) and lethal B20 (lB20). The variance in bristle number attributable to the tuh-1 locus in nature is approximately 10.1%, an indication that the bristle phenotype is most likely a neutral, pleiotrophic side effect of tuh-1.

摘要

tuh-1母体效应基因座包含两个天然存在的异等位基因,tuh-1h和tuh-1g。直到最近,除了评估它们对双胸复合体(BXC)腹部B(Abd-B)突变体tuh-3的影响外,还没有可能区分tuh-1h和tuh-1g的母体效应。然而,在本报告中,我们鉴定出一种与tuh-1基因座相关的刚毛表型,它具有非常有趣的进化意义。tuh-1h纯合雌性产生的成年后代的刚毛总是比tuh-1g纯合或杂合雌性产生的成年后代更多。这种影响是全身性的。头部、胸部以及腹部前后部的刚毛数量都增加。tuh-1基因完全缺失的雌性产生的后代刚毛数量很高。因此,刚毛表型是由于母体贡献的tuh-1g因子缺失所致。遗传证据表明,刚毛表型是由tuh-1基因座引起的,并且tuh-1h对tuh-1g完全隐性。tuh-1基因座位于X染色体着丝粒附近的常染色质-β-异染色质交界处,缺失分析将该基因座定位在致死基因额外器官(eo)和致死B20(lB20)之间。在自然条件下,归因于tuh-1基因座的刚毛数量变异约为10.1%,这表明刚毛表型很可能是tuh-1的一种中性、多效性副作用。

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