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集胞藻PCC 6803中cAMP和cGMP信号成分的基因组调查

Genomic survey of cAMP and cGMP signalling components in the cyanobacterium Synechocystis PCC 6803.

作者信息

Ochoa de Alda Jesús A G, Houmard Jean

机构信息

Dynamique des Membranes Végétales, Complexes Protéines-Pigments, CNRS UMR 8543, Ecole Normale Supérieure, 46 rue d'Ulm 75230 Paris Cedex 05, France1.

出版信息

Microbiology (Reading). 2000 Dec;146 Pt 12:3183-3194. doi: 10.1099/00221287-146-12-3183.

Abstract

Cyanobacteria modulate intracellular levels of cAMP and cGMP in response to environmental conditions (light, nutrients and pH). In an attempt to identify components of the cAMP and cGMP signalling pathways in Synechocystis PCC 6803, the authors screened its complete genome sequence by using bioinformatic tools and data from sequence-function studies performed on both eukaryotic and prokaryotic cAMP/cGMP-dependent proteins. Sll1624 and Slr2100 were tentatively assigned as being two putative cyclic nucleotide phosphodiesterases. Five proteins were identified as having all the determinants required to be cyclic nucleotide receptors, two of them being probably more specific for cGMP (an element of two-component regulatory systems - Slr2104 - and a putative cyclic-nucleotide-gated cation channel - Slr1575), the three others being probably more specific for cAMP: (i) a protein of unidentified function (Slr0842); (ii) a putative cyclic-nucleotide-modulated permease (Slr0593), previously annotated as a kinase A regulatory subunit; and (iii) a putative transcription factor (CRP-SYN: =Sll1371), which possesses cAMP- and DNA-binding determinants homologous to those of the cAMP receptor protein of Escherichia coli (CRP-EC:). This homology, together with the presence in Synechocystis of CRP-EC:-like binding sites upstream of crp, cya1, slr1575, and several genes encoding enzymes involved in transport and metabolism, strongly suggests that CRP-SYN: is a global regulator.

摘要

蓝细菌会根据环境条件(光照、营养物质和pH值)调节细胞内cAMP和cGMP的水平。为了鉴定集胞藻PCC 6803中cAMP和cGMP信号通路的组成成分,作者利用生物信息学工具以及对真核和原核cAMP/cGMP依赖性蛋白进行的序列功能研究数据,对其完整基因组序列进行了筛选。Sll1624和Slr2100被初步认定为两个假定的环核苷酸磷酸二酯酶。鉴定出五种蛋白具有作为环核苷酸受体所需的所有决定因素,其中两种可能对cGMP更具特异性(双组分调节系统的一个元件——Slr2104——和一个假定的环核苷酸门控阳离子通道——Slr1575),另外三种可能对cAMP更具特异性:(i)一种功能未知的蛋白(Slr0842);(ii)一种假定的环核苷酸调节通透酶(Slr0593),先前被注释为激酶A调节亚基;(iii)一种假定的转录因子(CRP-SYN:=Sll1371),它具有与大肠杆菌cAMP受体蛋白(CRP-EC)同源的cAMP和DNA结合决定因素。这种同源性,以及在集胞藻中crp、cya1、slr1575上游存在类似CRP-EC的结合位点,以及几个编码参与运输和代谢的酶的基因,强烈表明CRP-SYN是一种全局调节因子。

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