Transcriptional analysis of the conserved ftsZ gene cluster in Mycoplasma genitalium and Mycoplasma pneumoniae

被引:26
作者
Benders, GA
Powell, BC
Hutchison, CA
机构
[1] Univ N Carolina, Curriculum Genet & Mol Biol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
关键词
D O I
10.1128/JB.187.13.4542-4551.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Several experimental approaches were used to construct a detailed transcriptional profile of the phylogenetically conserved ftsZ cell division gene cluster in both Mycoplasma genitalium and its closest relative, Mycoplasma pneumoniae. We determined initiation and termination points for the cluster, as well as an absolute steady-state RNA level for each gene. Transcription of this cluster in both these organisms was shown to be highly strand specific. While the four genes in this cluster are cotranscribed, their transcription unit also includes two genes of close proximity yet disparate function. A transcription initiation point immediately upstream of these two genes was detected in M. genitalium but not M. pneumoniae. In M. pneumoniae, transcription of the six genes terminates at a poly(U)-tailed hairpin. In M. genitalium, this transcription terminates at two closely spaced points by an unknown mechanism. Real-time reverse transcription-PCR analysis of this cluster in M. pneumoniae shows that mRNA levels for all six genes vary at most fivefold and form a gradient of decreasing quantity with increasing distance from the promoter at the beginning of the cluster. mRNA from coding regions was approximately 20- to 100-fold more abundant than that from intergenic regions. We estimated the most abundant mRNA we detected at 0.6 copy per cell. We conclude that groups of functionally related genes in M. genitalium and M. pneumoniae are often preceded by promoters but rarely followed by terminators. This causes functionally unrelated genes to be commonly cotranscribed in these organisms.
引用
收藏
页码:4542 / 4551
页数:10
相关论文
共 35 条
[1]   A genome-based approach for the identification of essential bacterial genes [J].
Arigoni, F ;
Talabot, F ;
Peitsch, M ;
Edgerton, MD ;
Meldrum, E ;
Allet, E ;
Fish, R ;
Jamotte, T ;
Curchod, ML ;
Loferer, H .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :851-856
[2]   A putative transcription factor inducing mobility in Mycoplasma pneumoniae [J].
Bornberg-Bauer, E ;
Weiner, J .
MICROBIOLOGY-SGM, 2002, 148 :3764-3765
[3]   mraW, an essential gene at the dcw cluster of Escherichia coli codes for a cytoplasmic protein with methyltransferase activity [J].
Carrión, M ;
Gómez, MJ ;
Merchante-Schubert, R ;
Dongarrá, S ;
Ayala, JA .
BIOCHIMIE, 1999, 81 (8-9) :879-888
[4]   Crystal structure of a protein associated with cell division from Mycoplasma pneumoniae (GI: 13508053):: A novel fold with a conserved sequence motif [J].
Chen, SF ;
Jancrick, J ;
Yokota, H ;
Kim, R ;
Kim, SH .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2004, 55 (04) :785-791
[5]   RNA processing and degradation in Bacillus subtilis [J].
Condon, C .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (02) :157-+
[6]   Development of a strand-specific RT-PCR based assay to detect the replicative form of hepatitis C virus RNA [J].
Craggs, JK ;
Ball, JK ;
Thomson, BJ ;
Irving, WL ;
Grabowska, AM .
JOURNAL OF VIROLOGICAL METHODS, 2001, 94 (1-2) :111-120
[7]   A new essential gene of the 'minimal genome' affecting cell division [J].
Dassain, M ;
Leroy, A ;
Colosetti, L ;
Carolé, S ;
Bouché, JP .
BIOCHIMIE, 1999, 81 (8-9) :889-895
[8]   Disruption of gene mg218 of Mycoplasma genitalium through homologous recombination leads to an adherence-deficient phenotype [J].
Dhandayuthapani, S ;
Rasmussen, WG ;
Baseman, JB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) :5227-5232
[9]   The immunoreactive 116 kDa surface protein of Mycoplasma pneumoniae is encoded in an operon [J].
Duffy, MF ;
Walker, ID ;
Browning, GF .
MICROBIOLOGY-UK, 1997, 143 :3391-3402
[10]   Prediction of transcription terminators in bacterial genomes [J].
Ermolaeva, MD ;
Khalak, HG ;
White, O ;
Smith, HO ;
Salzberg, SL .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 301 (01) :27-33