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黑腹果蝇的原始突变体:嘧啶营养缺陷型细胞系的分离与鉴定

Rudimentary mutants ofDrosophila melanogaster : Isolation and characterization of pyrimidine auxotrophic cell lines.

作者信息

Regenass Urs, Bernhard Hans Peter

机构信息

Department of Cell Biology, Biozentrum, University of Basel, Klingelbergstr. 70, CH-4056, Basel, Switzerland.

出版信息

Wilehm Roux Arch Dev Biol. 1979 Jun;187(2):167-177. doi: 10.1007/BF00848269.

Abstract

The X-linkedrudimentary (r) mutants ofDrosophila melanogaster are pyrimidine auxotrophs and require exogenous pyrimidines (Nørby, 1970; Falk, 1976). We have established a set ofrudimentary cell lines that are derived from embryos, homozygous for eitherr orr . The enzymatic activities of the pyrimidine synthesizing enzymes were measured in the mutant lines. We have further investigated the nutritional requirements of the mutant cells in vitro by using a pyrimidine free culture medium.Ther cell lines were found to express 3-7%dihydroorotase (DHOase) activity as compared to a wildtype cell line. Reducedaspartate transcarbamylase (ATCase) activity was measured in somer cell lines whereas wildtypecarbamylphosphate synthetase (CPSase) activity is expressed in allr cell lines. Ther cell line expresses wildtype activity ofDHOase andCPSase. ATCase activity was found to be reduced to 10% of the wildtype activity.The mutant cell lines do not proliferate in pyrimidine free minimal medium and cell proliferation is obtained by the addition of crude RNA. Proliferation of ther cells is restored by the supplementation of the minimal medium withdihydroorotate whereas proliferation of ther cells is restored by supplementation with eitherdihydroorotate orcarbamylaspartate.The results demonstrate that therudimentary phenotypesr andr are expressed at the cellular level and that the two mutant cell types behave as cellular pyrimidine auxotrophs in vitro.

摘要

果蝇黑腹果蝇的X连锁发育不全(r)突变体是嘧啶营养缺陷型,需要外源性嘧啶(诺比,1970;福尔克,1976)。我们建立了一组发育不全细胞系,这些细胞系来源于纯合子r或r的胚胎。在突变细胞系中测量了嘧啶合成酶的酶活性。我们进一步使用无嘧啶培养基在体外研究了突变细胞的营养需求。与野生型细胞系相比,发现r细胞系表达3 - 7%的二氢乳清酸酶(DHOase)活性。在一些r细胞系中测量到天冬氨酸转氨甲酰酶(ATCase)活性降低,而所有r细胞系均表达野生型氨甲酰磷酸合成酶(CPSase)活性。r细胞系表达DHOase和CPSase的野生型活性。发现ATCase活性降低至野生型活性的10%。突变细胞系在无嘧啶基本培养基中不增殖,通过添加粗RNA可实现细胞增殖。通过在基本培养基中添加二氢乳清酸可恢复r细胞的增殖,而通过添加二氢乳清酸或氨甲酰天冬氨酸可恢复r细胞的增殖。结果表明,发育不全表型r和r在细胞水平上表达,并且这两种突变细胞类型在体外表现为细胞嘧啶营养缺陷型。

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