Characterizations of Highly Expressed Genes of Four Fast-Growing Bacteria

Author:

Karlin Samuel1,Mrázek Jan1,Campbell Allan2,Kaiser Dale3

Affiliation:

1. Department of Mathematics, Stanford University, Stanford, California 94305-21251;

2. Department of Biological Sciences, Stanford University, Stanford, California 94305-20502; and

3. Department of Biochemistry, Stanford University, Stanford, California 94305-53073

Abstract

ABSTRACT Predicted highly expressed (PHX) genes are characterized for the completely sequenced genomes of the four fast-growing bacteria Escherichia coli, Haemophilus influenzae, Vibrio cholerae, and Bacillus subtilis . Our approach to ascertaining gene expression levels relates to codon usage differences among certain gene classes: the collection of all genes (average gene), the ensemble of ribosomal protein genes, major translation/transcription processing factors, and genes for polypeptides of chaperone/degradation complexes. A gene is predicted highly expressed (PHX) if its codon frequencies are close to those of the ribosomal proteins, major translation/transcription processing factor, and chaperone/degradation standards but strongly deviant from the average gene codon frequencies. PHX genes identified by their codon usage frequencies among prokaryotic genomes commonly include those for ribosomal proteins, major transcription/translation processing factors (several occurring in multiple copies), and major chaperone/degradation proteins. Also PHX genes generally include those encoding enzymes of essential energy metabolism pathways of glycolysis, pyruvate oxidation, and respiration (aerobic and anaerobic), genes of fatty acid biosynthesis, and the principal genes of amino acid and nucleotide biosyntheses. Gene classes generally not PHX include most repair protein genes, virtually all vitamin biosynthesis genes, genes of two-component sensor systems, most regulatory genes, and most genes expressed in stationary phase or during starvation. Members of the set of PHX aminoacyl-tRNA synthetase genes contrast sharply between genomes. There are also subtle differences among the PHX energy metabolism genes between E. coli and B. subtilis , particularly with respect to genes of the tricarboxylic acid cycle. The good agreement of PHX genes of E. coli and B. subtilis with high protein abundances, as assessed by two-dimensional gel determination, is verified. Relationships of PHX genes with stoichiometry, multifunctionality, and operon structures are also examined. The spatial distribution of PHX genes within each genome reveals clusters and significantly long regions without PHX genes.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference52 articles.

1. Aizawa S.-I. I. B. Zhulin L. Marquez-Magana and G. W. Ordal. Chemotaxis and motility in Bacillus subtilis. In A. L. Sonenshein (ed.) Bacillus subtilis 2nd ed. in press. ASM Press Washington D.C.

2. Bacillus subtilis aconitase is an RNA-binding protein;Alén C.;Proc. Natl. Acad. Sci. USA,1999

3. First steps from two-dimensional protein index towards a response regulation map for Bacillus subtilis;Antelmann H.;Electrophoresis,1997

4. Conformational independence of N- and C-domains in ribosomal protein L7/L12 and in the complex with protein L10;Bocharov E. V.;FEBS Lett.,1998

5. A symmetric-iterated multiple alignment of protein sequences;Brocchieri L.;J. Mol. Biol.,1998

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3