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盘基网柄菌早期发育基因在信号转导突变体中的调控

Regulation of Dictyostelium early development genes in signal transduction mutants.

作者信息

Wu L, Hansen D, Franke J, Kessin R H, Podgorski G J

机构信息

Department of Anatomy and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.

出版信息

Dev Biol. 1995 Sep;171(1):149-58. doi: 10.1006/dbio.1995.1267.

Abstract

The secreted cyclic nucleotide phosphodiesterase (PDE) and its glycoprotein inhibitor (PDI) are among the first genes expressed when Dictyostelium amoebae begin their development. We used a series of mutants with defects in signal transduction to ask whether cAMP receptors 1 and 3, G alpha2, G beta, adenylyl cyclase (ACA), or the protein kinase A catalytic subunit (PKAcat) are required for the initial appearance or later regulation of the PDE and the PDI transcripts. The PDE gene produces a 1.9-kb transcript during vegetative growth and then a 2.4-kb transcript during the early hours of development. Regulation of the 2.4-kb transcript in CAR1, G alpha2, G beta, and ACA mutants is similar to that of isogenic parental strains, although its level is reduced in strains that carry the CAR1 mutation. CAR1/CAR3 double mutants also produce less PDE transcript, but the PDE gene remains inducible by cAMP. The PKAcat mutant produces the 2.4-kb PDE transcript, but in this mutant the vegetative transcript is retained in development. CAR1 and CAR3 are not required for transcription of the PDI gene, but deleting CAR1 leads to overproduction of the PDI transcript. Induction or repression of the PDI gene does not require G alpha2, G beta, or ACA. PKAcat is required for synthesis of the PDI transcript. The results suggest a two-stage regulation of these early genes through a G alpha2/G beta-independent mechanism and an absolute dependence of PDI on the PKAcat.

摘要

分泌型环核苷酸磷酸二酯酶(PDE)及其糖蛋白抑制剂(PDI)是盘基网柄菌变形虫开始发育时最早表达的基因之一。我们使用了一系列信号转导有缺陷的突变体,来探究cAMP受体1和3、Gα2、Gβ、腺苷酸环化酶(ACA)或蛋白激酶A催化亚基(PKAcat)对于PDE和PDI转录本的初始出现或后期调控是否是必需的。PDE基因在营养生长期间产生一个1.9 kb的转录本,然后在发育早期产生一个2.4 kb的转录本。在CAR1、Gα2、Gβ和ACA突变体中,2.4 kb转录本的调控与同基因亲本菌株相似,尽管在携带CAR1突变的菌株中其水平有所降低。CAR1/CAR3双突变体也产生较少的PDE转录本,但PDE基因仍可被cAMP诱导。PKAcat突变体产生2.4 kb的PDE转录本,但在这个突变体中,营养期转录本在发育过程中得以保留。PDI基因的转录不需要CAR1和CAR3,但缺失CAR1会导致PDI转录本的过量产生。PDI基因的诱导或抑制不需要Gα2、Gβ或ACA。PKAcat是PDI转录本合成所必需的。结果表明,这些早期基因通过一种不依赖Gα2/Gβ的机制进行两阶段调控,并且PDI绝对依赖于PKAcat。

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