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果蝇中dco基因突变导致的间隙连接通讯缺陷与成虫盘过度生长和退化相关。

Defective gap-junctional communication associated with imaginal disc overgrowth and degeneration caused by mutations of the dco gene in Drosophila.

作者信息

Jursnich V A, Fraser S E, Held L I, Ryerse J, Bryant P J

机构信息

Developmental Biology Center, University of California, Irvine 92717.

出版信息

Dev Biol. 1990 Aug;140(2):413-29. doi: 10.1016/0012-1606(90)90090-6.

Abstract

The lethal(3)discs overgrown (dco) locus of Drosophila melanogaster, located on the third chromosome at cytogenetic position 100A5,6-100B1,2, is necessary for normal development and growth control in the imaginal discs of the larva. Three recessive lethal alleles (dco2, dco3, and dco18) in heteroallelic combinations and one allele (dco3) when homozygous cause the imaginal discs to continue to grow beyond the normal disc-intrinsic limit during an extended larval period. Some degeneration also occurs in the overgrowing discs. The discs overgrow even when transplanted early in their development into wild-type hosts, whereas normal discs stop growth at about the normal final size under such conditions, indicating that the overgrowth is a disc-autonomous effect of the mutations. During overgrowth the imaginal discs retain their single-layered epithelial structure except near regions of degeneration, and they differentiate into disc-appropriate but abnormal adult structures when transplanted into wild-type larval hosts. When the mutant larvae are reared under certain conditions a small percentage develop to the pharate adult stage, and these animals show a characteristic syndrome of abnormalities including swollen leg segments with many extra bristles, small or missing eyes, duplicated antennae and palpi, and separated vesicles of cuticle. A fourth recessive lethal allele (dcole88), when homozygous or in heteroallelic combination with the overgrowth alleles, causes the imaginal discs to degenerate, producing a "discless" phenotype. Gap junction-mediated communication was assayed by observing the intercellular transfer of injected fluorescein complexon (dye coupling). Dye coupling in the imaginal discs of the dco genotypes that cause overgrowth was dramatically reduced at 4 days after egg laying (AEL) compared with wild-type controls. Coupling was more normal although still significantly reduced at 7-8 and 12-14 days AEL. In c43hs1, another disc overgrowth mutant, the imaginal disc cells also showed very reduced dye coupling at 4 days and incomplete coupling at 9 days. In contrast, discs from wild-type larvae, two other imaginal disc overgrowth mutants, and a cell death mutant showed extensive dye coupling at all stages tested. Electron microscopic morphometry revealed a reduction in gap-junction length per unit lateral plasma membrane length in dco3/dco18 and c43hs1 wing discs, although not in dco2/dco3, compared with wild-type wing discs. The results suggest that gap-junctional cell communication may be involved in the cell interactions that limit cell proliferation in vivo.

摘要

黑腹果蝇的致死(3)盘过度生长(dco)基因座位于第三染色体的细胞遗传学位置100A5,6 - 100B1,2,对于幼虫成虫盘的正常发育和生长控制是必需的。三个隐性致死等位基因(dco2、dco3和dco18)以杂合等位基因组合形式存在,以及一个等位基因(dco3)纯合时,会导致成虫盘在延长的幼虫期内持续生长超过正常的盘内在生长极限。在过度生长的盘中也会发生一些退化。即使在发育早期将这些盘移植到野生型宿主体内,它们仍会过度生长,而正常盘在这种情况下会在接近正常最终大小时停止生长,这表明过度生长是突变的盘自主效应。在过度生长期间,成虫盘除了在退化区域附近外,保留其单层上皮结构,并且当移植到野生型幼虫宿主体内时,它们会分化为与盘相应但异常的成虫结构。当突变幼虫在特定条件下饲养时,一小部分会发育到准成虫阶段,这些动物表现出一种特征性的异常综合征,包括腿部节段肿胀且有许多额外刚毛、眼睛小或缺失、触角和触须重复以及表皮小泡分离。第四个隐性致死等位基因(dcole88),纯合或与过度生长等位基因以杂合等位基因组合形式存在时,会导致成虫盘退化,产生“无盘”表型。通过观察注射的荧光素络合物的细胞间转移(染料偶联)来检测间隙连接介导的通讯。与野生型对照相比,导致过度生长的dco基因型成虫盘中的染料偶联在产卵后4天(AEL)显著减少。在7 - 8天和12 - 14天AEL时,偶联更为正常,尽管仍显著减少。在另一个盘过度生长突变体c43hs1中,成虫盘细胞在4天时染料偶联也非常减少,在9天时偶联不完全。相比之下,野生型幼虫的盘、另外两个成虫盘过度生长突变体的盘以及一个细胞死亡突变体的盘在所有测试阶段都显示出广泛的染料偶联。电子显微镜形态计量学显示,与野生型翅盘相比,dco3/dco18和c43hs1翅盘中单位侧向质膜长度的间隙连接长度减少,尽管dco2/dco3中没有减少。结果表明,间隙连接介导的细胞通讯可能参与了体内限制细胞增殖的细胞相互作用。

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