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Ribosomal protein insufficiency and the minute syndrome in Drosophila: a dose-response relationship.

机译:果蝇中的核糖体蛋白不足和微小综合症:剂量反应关系。

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摘要

Minutes comprise > 50 phenotypically similar mutations scattered throughout the genome of Drosophila, many of which are identified as mutations in ribosomal protein (rp) genes. Common traits of the Minute phenotype are short and thin bristles, slow development, and recessive lethality. By mobilizing a P element inserted in the 5' UTR of M(3)95A, the gene encoding ribosomal protein S3 (RPS3), we have generated two homozygous viable heteroalleles that are partial revertants with respect to the Minute phenotype. Molecular characterization revealed both alleles to be imprecise excisions, leaving 40 and 110 bp, respectively, at the P-element insertion site. The weaker allele (40 bp insert) is associated with a approximately 15% decrease in RPS3 mRNA abundance and displays a moderate Minute phenotype. In the stronger allele (110 bp insert) RPS3 mRNA levels are reduced by approximately 60%, resulting in an extreme Minute phenotype that includes many morphological abnormalities as well as sterility in both males and females due to disruption of early gametogenesis. The results show that there is a correlation between reduced RPS3 mRNA levels and the severity of the Minute phenotype, in which faulty differentiation of somatic tissues and arrest of gametogenesis represent the extreme case. That heteroalleles in M(3)95A can mimic the phenotypic variations that exist between different Minute/rp-gene mutations strongly suggests that all phenotypes primarily are caused by reductions in maximum protein synthesis rates, but that the sensitivity for reduced levels of the individual rp-gene products is different.
机译:分钟包括果蝇全基因组中散布的> 50个表型相似的突变,其中许多被鉴定为核糖体蛋白(rp)基因中的突变。分钟表型的共同特征是鬃毛短而细,发育缓慢和隐性杀伤力。通过动员插入编码核糖体蛋白S3(RPS3)的基因M(3)95A的5'UTR中的P元素,我们产生了两个纯合的活杂种等位基因,它们是关于Minute表型的部分回复。分子表征揭示两个等位基因都是不精确的切除,分别在P元素插入位点留下40和110 bp。较弱的等位基因(40 bp插入片段)与RPS3 mRNA丰度降低约15%相关,并表现出中等的Minute表型。在较强的等位基因(插入片段为110 bp)中,RPS3 mRNA水平降低了约60%,导致极端的分钟表型,其中包括许多形态异常以及由于早期配子发生的中断而导致的雄性和雌性不育。结果表明,降低的RPS3 mRNA水平与Minute表型的严重程度之间存在相关性,其中体细胞组织的错误分化和配子发生的停止代表了极端情况。 M(3)95A中的杂等位基因可以模拟不同Minute / rp基因突变之间存在的表型变异,这强烈表明所有表型主要是由最大蛋白质合成速率的降低引起的,但是对于降低单个rp水平的敏感性基因产品是不同的。

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