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Deduced product of the stage 0 sporulation gene spo0F shares homology with the Spo0A, OmpR, and SfrA proteins.

作者信息

Trach K A, Chapman J W, Piggot P J, Hoch J A

出版信息

Proc Natl Acad Sci U S A. 1985 Nov;82(21):7260-4. doi: 10.1073/pnas.82.21.7260.

DOI:10.1073/pnas.82.21.7260
PMID:2997779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC390829/
Abstract

The location of the stage 0 sporulation locus spo0F has been determined on a cloned fragment of Bacillus subtilis DNA. The spo0F gene and surrounding region was sequenced and was shown to code for a protein of Mr 14,286. The amino acid sequence of this deduced protein was 56% homologous to the amino-terminal domain of the spo0A gene product. The molecular weight of the Spo0F protein was approximately half that of the Spo0A protein, and its sequence was homologous to the amino-terminal half of the Spo0A protein. This same portion of the Spo0A protein showed ancestral relationship to the OmpR and SfrA regulatory proteins of Escherichia coli. Mutations in any of the genes encoding these proteins in either organism are highly pleiotropic and result in alterations in the regulation of membrane components, suggesting that they may have related roles in both organisms and that the stage 0 sporulation defect of spo0A and spo0F mutants is an indirect consequence of this regulatory system.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f50/390829/f7bfdb67fc6b/pnas00361-0115-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f50/390829/050667b30db2/pnas00361-0114-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f50/390829/f7bfdb67fc6b/pnas00361-0115-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f50/390829/050667b30db2/pnas00361-0114-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f50/390829/f7bfdb67fc6b/pnas00361-0115-a.jpg

相似文献

1
Deduced product of the stage 0 sporulation gene spo0F shares homology with the Spo0A, OmpR, and SfrA proteins.
Proc Natl Acad Sci U S A. 1985 Nov;82(21):7260-4. doi: 10.1073/pnas.82.21.7260.
2
Characterization of the spo0A locus and its deduced product.spo0A基因座及其推导产物的特征分析。
Proc Natl Acad Sci U S A. 1985 May;82(9):2647-51. doi: 10.1073/pnas.82.9.2647.
3
Characterization of the gene for a protein kinase which phosphorylates the sporulation-regulatory proteins Spo0A and Spo0F of Bacillus subtilis.对一种蛋白激酶基因的特性研究,该蛋白激酶可使枯草芽孢杆菌的孢子形成调节蛋白Spo0A和Spo0F发生磷酸化。
J Bacteriol. 1989 Nov;171(11):6187-96. doi: 10.1128/jb.171.11.6187-6196.1989.
4
Revised assignment for the Bacillus subtilis spo0F gene and its homology with spo0A and with two Escherichia coli genes.枯草芽孢杆菌spo0F基因的修订任务及其与spo0A和两个大肠杆菌基因的同源性。
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5
Dimer form of phosphorylated Spo0A, a transcriptional regulator, stimulates the spo0F transcription at the initiation of sporulation in Bacillus subtilis.磷酸化的Spo0A(一种转录调节因子)的二聚体形式在枯草芽孢杆菌芽孢形成起始阶段刺激spo0F转录。
J Mol Biol. 1995 Jun 30;250(1):11-23. doi: 10.1006/jmbi.1995.0354.
6
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A positive feedback loop controls transcription of the spoOF gene, a component of the sporulation phosphorelay in Bacillus subtilis.一个正反馈环控制着枯草芽孢杆菌中芽孢形成磷酸信号转导途径的一个组成部分spoOF基因的转录。
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Signal transduction and sporulation in Bacillus subtilis: autophosphorylation of Spo0A, a sporulation initiation gene product.枯草芽孢杆菌中的信号转导与芽孢形成:芽孢形成起始基因产物Spo0A的自磷酸化作用
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Mol Microbiol. 1988 Nov;2(6):689-99. doi: 10.1111/j.1365-2958.1988.tb00079.x.

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REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS.枯草芽孢杆菌转化的要求。
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1H, 15N, and 13C backbone chemical shift assignments, secondary structure, and magnesium-binding characteristics of the Bacillus subtilis response regulator, Spo0F, determined by heteronuclear high-resolution NMR.通过异核高分辨率核磁共振确定的枯草芽孢杆菌应答调节因子Spo0F的1H、15N和13C主链化学位移归属、二级结构及镁结合特性。
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Temperature-sensitive sporulation caused by a mutation in the Bacillus subtilis secY gene.枯草芽孢杆菌secY基因突变导致的温度敏感型芽孢形成
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Early sporulation gene spo0F: nucleotide sequence and analysis of gene product.早期芽孢形成基因spo0F:核苷酸序列及基因产物分析
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Developmental and genetic regulation of Bacillus subtilis genes transcribed by sigma 28-RNA polymerase.由σ28-RNA聚合酶转录的枯草芽孢杆菌基因的发育和遗传调控。
Cell. 1983 Nov;35(1):285-93. doi: 10.1016/0092-8674(83)90231-3.
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A reliable method for the recovery of DNA fragments from agarose and acrylamide gels.一种从琼脂糖凝胶和丙烯酰胺凝胶中回收DNA片段的可靠方法。
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Sequencing end-labeled DNA with base-specific chemical cleavages.通过碱基特异性化学切割对末端标记的DNA进行测序。
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