Genes involved in cell division in mycoplasmas

被引:14
作者
Alarcon, Frank
Ribeiro de Vasconcelos, Ana Tereza
Yim, Lucia
Zaha, Arnaldo
机构
[1] Univ Fed Rio Grande do Sul, Ctr Biotecnol, BR-91501970 Porto Alegre, RS, Brazil
[2] Minist Ciencia & Tecnol, Lab Nacl Computacao Cientif, Petropolis, RJ, Brazil
[3] Inst Biol Mol Parana, Curitiba, Parana, Brazil
关键词
cell division; Mycoplasma spp; genomes;
D O I
10.1590/S1415-47572007000200003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacterial cell division has been studied mainly in model systems such as Escherichia coli and Bacillus subtilis, where it is described as a complex process with the participation of a group of proteins which assemble into a multiprotein complex called the septal ring. Mycoplasmas are cell wall-less bacteria presenting a reduced genome. Thus, it was important to compare their genomes to analyze putative genes involved in cell division processes. The division and cell wall (dcw) cluster, which in E coli and B. subtilis is composed of 16 and 17 genes, respectively, is represented by only three to four genes in mycoplasmas. Even the most conserved protein, FtsZ, is not present in all mycoplasma genomes analyzed so far. A model for the FtsZ protein from Mycoplasma hyopneumoniae and Mycoplasma synoviae has been constructed. The conserved residues, essential for GTP/GDP binding, are present in FtsZ from both species. A strong conservation of hydrophobic amino acid patterns is observed, and is probably necessary for the structural stability of the protein when active. M. synoviae FtsZ presents an extended amino acid sequence at the C-terminal portion of the protein, which may participate in interactions with other still unknown proteins crucial for the cell division process.
引用
收藏
页码:174 / 181
页数:8
相关论文
共 42 条
[1]   A System for Automated Bacterial (genome) Integrated Annotation - SABIA [J].
Almeida, LGP ;
Paixao, R ;
Souza, RC ;
da Costa, GC ;
Barrientos, FJA ;
dos Santos, MT ;
de Almeida, DF ;
Vasconcelos, ATR .
BIOINFORMATICS, 2004, 20 (16) :2832-2833
[2]   IMPAIRED CELL-DIVISION AND SPORULATION OF A BACILLUS-SUBTILIS STRAIN WITH THE FTSA GENE DELETED [J].
BEALL, B ;
LUTKENHAUS, J .
JOURNAL OF BACTERIOLOGY, 1992, 174 (07) :2398-2403
[3]   Transcriptional analysis of the conserved ftsZ gene cluster in Mycoplasma genitalium and Mycoplasma pneumoniae [J].
Benders, GA ;
Powell, BC ;
Hutchison, CA .
JOURNAL OF BACTERIOLOGY, 2005, 187 (13) :4542-4551
[4]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[5]   FtsK activities in Xer recombination, DNA mobilization and cell division involve overlapping and separate domains of the protein [J].
Bigot, S ;
Corre, J ;
Louarn, JM ;
Cornet, F ;
Barre, FX .
MOLECULAR MICROBIOLOGY, 2004, 54 (04) :876-886
[6]   Crystal structure of the SOS cell division inhibitor SulA and in complex with FtsZ [J].
Cordell, SC ;
Robinson, EJH ;
Löwe, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (13) :7889-7894
[7]   Role of penicillin-binding protein PBP2B in assembly and functioning of the division machinery of Bacillus subtilis [J].
Daniel, RA ;
Harry, EJ ;
Errington, J .
MOLECULAR MICROBIOLOGY, 2000, 35 (02) :299-311
[8]   Intrinsic instability of the essential cell division protein FtsL of Bacillus subtilis and a role for DivIB protein in FtsL turnover [J].
Daniel, RA ;
Errington, J .
MOLECULAR MICROBIOLOGY, 2000, 36 (02) :278-289
[9]   Cytokinesis in bacteria [J].
Errington, J ;
Daniel, RA ;
Scheffers, DJ .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (01) :52-+
[10]   A physical and functional interaction between Escherichia coli FtsK and topoisomerase IV [J].
Espeli, O ;
Lee, C ;
Marians, KJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (45) :44639-44644