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黑腹果蝇中不能飞行突变体的分离与鉴定

Isolation and characterization of flightless mutants in Drosophila melanogaster.

作者信息

Koana T, Hotta Y

出版信息

J Embryol Exp Morphol. 1978 Jun;45:123-43.

PMID:97355
Abstract

Since animal behaviour is executed through neuronal circuits including sensory receptors and muscle, genes vital for their development and differentiation must be found among mutants having behavioural anomaly. After mutagenesis with ethyl methanesulphonate (EMS), we screened for X-linked flightless mutants of Drosophila melanogaster by using column-type flight tester. Approximately 10(4) individuals were screened and 21 mutant genes were isolated. Chromosomal mapping and complementation experiments revealed that they belong to 15 cistrons randomly located on X chromosome, three cistrons having more than two alleles. Two of the isolated mutants (fltO2 and fltH, which are recessive both behaviourally and morphologically) were analysed with the mosaic fate mapping technique, and both were found to have their primary foci in mesodermal region of blastoderm, suggesting that the genes exert their primary effect in indirect flight muscle. Electronmicroscopic studies on the muscles from four alleles of the fltO2 cistron revealed an abnormality in myofibrillar arrangement. A possible deficit within Z-band components is discussed in relation to wings-up B mutants. The indirect flight muscle of flltH was also examined, and it was found that sarcomere length and diameter of myofibrils were abnormal. It was postulated that a possible factor which controls size of myofibrils is defective in this mutant. These examples indicate the advantage of combining ultrastructural examination with genetic mosaic mapping technique.

摘要

由于动物行为是通过包括感觉感受器和肌肉在内的神经回路来执行的,因此在具有行为异常的突变体中必定能找到对其发育和分化至关重要的基因。在用甲磺酸乙酯(EMS)诱变后,我们使用柱式飞行测试仪筛选了黑腹果蝇的X连锁不能飞行突变体。大约筛选了10⁴个个体,并分离出21个突变基因。染色体定位和互补实验表明,它们属于随机位于X染色体上的15个顺反子,其中三个顺反子有两个以上的等位基因。对分离出的两个突变体(fltO2和fltH,它们在行为和形态上均为隐性)采用镶嵌命运图谱技术进行了分析,发现二者的主要病灶都在胚盘的中胚层区域,这表明这些基因在间接飞行肌中发挥主要作用。对fltO2顺反子的四个等位基因的肌肉进行的电子显微镜研究揭示了肌原纤维排列异常。结合翅膀上举B突变体讨论了Z带成分中可能存在的缺陷。还对flltH的间接飞行肌进行了检查,发现肌原纤维的肌节长度和直径异常。据推测,该突变体中一个控制肌原纤维大小的可能因子存在缺陷。这些例子表明了将超微结构检查与遗传镶嵌图谱技术相结合的优势。

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