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果蝇致死(1)盘状大蛋白-1致癌基因的分子克隆。

Molecular cloning of the lethal(1)discs large-1 oncogene of Drosophila.

作者信息

Woods D F, Bryant P J

机构信息

Developmental Biology Center, University of California, Irvine 92717.

出版信息

Dev Biol. 1989 Jul;134(1):222-35. doi: 10.1016/0012-1606(89)90092-4.

Abstract

We present a genetic, developmental and molecular analysis of lethal(1)discs large-1[l(1)d.lg-1; Stewart et al., 1972], an oncogene of Drosophila. Mutations in this gene cause the imaginal discs to grow by cell proliferation beyond their normal final size, transform into solid tumors, fuse with one another and the brain, and lose their ability to differentiate. The oncogene represents the only known complementation group between two deficiency breakpoints, and 15 recessive lethal alleles are available. Cloning of the DNA between the two deficiency breakpoints defines a region of 45 +/- 2 kb. The l(1)d.lg-1 transcription unit is identified by both qualitative and quantitative effects of several l(1)d.lg-1 mutations on the RNA transcripts and by the presence of a DNA insert in one of the l(1)d.lg-1 alleles. It gives rise to at least five different transcripts ranging in size from 1.9 to 6.0 kb. Three other transcription units are present within this region, two 5' to the l(1)d.lg-1 gene and one at the 3' end. A near full-length cDNA from one of the larger transcripts of l(1)d.lg-1 has homology to genomic DNA spanning over 20 kb. A developmental profile of l(1)d.lg-1 transcription is presented. We discuss how mutations in this gene could disrupt epithelial structure and how this might be related to the excessive cell proliferation and interdisc fusion that is observed. We also compare this gene with another recessive oncogene of Drosophila, lethal(2)giant larvae, that has been cloned and characterized.

摘要

我们对果蝇的一个癌基因致死(1)盘大-1 [l(1)d.lg-1;Stewart等人,1972]进行了遗传、发育和分子分析。该基因的突变导致成虫盘通过细胞增殖生长超过其正常最终大小,转化为实体瘤,相互融合并与大脑融合,并丧失其分化能力。该癌基因是两个缺失断点之间唯一已知的互补群,有15个隐性致死等位基因可用。两个缺失断点之间的DNA克隆确定了一个45±2 kb的区域。通过几个l(1)d.lg-1突变对RNA转录本的定性和定量影响以及一个l(1)d.lg-1等位基因中存在DNA插入来鉴定l(1)d.lg-1转录单位。它产生至少五种不同大小的转录本,范围从1.9到6.0 kb。该区域内还存在另外三个转录单位,两个在l(1)d.lg-1基因的5'端,一个在3'端。来自l(1)d.lg-1较大转录本之一的近全长cDNA与跨越20 kb以上的基因组DNA具有同源性。给出了l(l)d.lg-1转录的发育概况。我们讨论了该基因中的突变如何破坏上皮结构以及这可能如何与观察到的过度细胞增殖和盘间融合相关。我们还将该基因与果蝇的另一个隐性癌基因致死(2)巨幼虫进行了比较,该基因已被克隆和表征。

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