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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >GENETIC AND DEVELOPMENTAL ANALYSIS OF A TEMPERATURE-SENSITIVE MINUTE MUTATION OF DROSOPHILA MELANOGASTER
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GENETIC AND DEVELOPMENTAL ANALYSIS OF A TEMPERATURE-SENSITIVE MINUTE MUTATION OF DROSOPHILA MELANOGASTER

机译:黑腹果蝇温度敏感性微小突变的遗传和发育分析

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摘要

A temperature-sensitive (ts) third chromosome Minute (M) mutation, designated Q-III, has been recovered and characterized. Q-III heterozygotes raised at 29" exhibit all of the dominant traits of M mutants including small bristles, rough eyes, prolonged development, reduced viability 2nd interactions with several unrelated mutations. Q-III homozygotes raised at 29° are lethal; death occurs primarily during the first larval instar. When raised at 22°, Q-Ill heterozygotes are phenotypically normal and Q-III homozygotes display moderate M traits. In addition, Q-III elicits ts sterility and maternal-effect lethality. As it true of M lesions, the dominant traits of Q-111 are not expressed in triploid females raised at 29°. Complementation tests suggest that Q-III is a ts allele of M(3)LS4, which is located in 3L near the centromere.——Reciprocal temperature-shift experiments revealed that the temperature-sensitive period (TSP) of Q-111 lethality is polyphasic, extending from the first instar to the latter half of pupation. Heat-pulse experiments further resolved this into two post-embryonic TSPs: one occurring during the latter half of the second larval instar, and the other extending from the larval/pupal boundary to the second half of pupation. In addition, heat pulses elicited a large number of striking adult phenotypes in Q-III individuals. These included pattern alterations such as deficiencies and duplications and cther morphological defects in structures produced by the eye-antennal, leg, wing and genital imaginal discs and the abdominal histoblasts. Each defect or pattern alteration is associated with a specific TSP during development.——We favor the interpretation that most of the major Q-III defects, particularly the structural duplications and deficiencies, result from temperature-induced cell death in mitotically active imaginal anlagen, while the small macrochaete phene probably results from the direct effects of Q-III on bristle synthesis. The hypothesis that the Q-III locus specifices a component required for protein synthesis is discussed, and it is concluded that this hypothesis can account for the pleiotropy of Q-III, and that perhaps it can be extended to M loci in general.
机译:温度敏感(ts)的第三染色体分钟(M)突变,称为Q-III,已被回收并鉴定。在29“处生长的Q-III杂合子表现出M突变体的所有显性特征,包括刚毛,眼睛粗糙,发育延长,存活力降低与一些无关突变的第二次相互作用。在29°升高的Q-III纯合子具有致命性;主要发生死亡。在第一个幼虫期时,Q-III杂合子在表型上是正常的,Q-III纯合子表现出中等的M特性,此外,Q-III引起不育和母性杀伤力。 ,在29°升高的三倍体雌性中没有表达Q-111的优势性状,互补性测试表明Q-III是M(3)LS4的ts等位基因,位于等位点附近3L。移位实验表明,Q-111致死率的温度敏感期(TSP)是多相的,从化star期开始到化p后期,热脉冲实验进一步将其分解为两个胚后TSP:一个发生在热休克期。环回第二个幼虫龄期的后半部,另一个从幼虫/ pu的边界延伸到化up的后半部。另外,热脉冲在Q-III个体中引起大量惊人的成年表型。这些包括图案变化,例如眼,肾,椎间盘,生殖器的假想椎间盘和腹部成纤维细胞产生的结构的缺陷和重复,以及其他形态的缺陷。在开发过程中,每种缺陷或模式的改变都与特定的TSP有关。——我们赞成这样一种解释,即大多数主要的Q-III缺陷,特别是结构重复和缺陷,是由有丝分裂活跃的想象中的胶原蛋白中温度诱导的细胞死亡引起的,而小的长毛象可能是Q-III对刷毛合成的直接影响。讨论了Q-III基因座特异于蛋白质合成所需成分的假说,并得出结论,该假说可以解释Q-III的多效性,并且也许可以将其扩展到M位点。

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