The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis

被引:186
作者
Chambaud, I
Heilig, R
Ferris, S
Barbe, V
Samson, D
Galisson, F
Moszer, I
Dybvig, K
Wróblewski, H
Viari, A
Rocha, EPC
Blanchard, A
机构
[1] Univ Bordeaux 2, INRA, Inst Biol Vegetale Mol, F-33883 Villenave Dornon, France
[2] Inst Pasteur, Unite Oncol Virale, F-75724 Paris 15, France
[3] Inst Pasteur, Serv Informat Sci, F-75724 Paris 15, France
[4] Inst Pasteur, Unite Regulat Express Genet, F-75724 Paris 15, France
[5] Ctr Natl Sequencage, Genoscope, F-91006 Evry, France
[6] Univ Alabama Birmingham, Dept Genom & Pathol, Birmingham, AL 35294 USA
[7] Univ Rennes 1, CNRS, UMR 6026, F-35042 Rennes, France
[8] INRIA Rhone Alpes, Projet HELIX, F-38330 Montbonnot St Martin, France
[9] Atelier Bioinformat, F-75005 Paris, France
关键词
D O I
10.1093/nar/29.10.2145
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
Mycoplasma pulmonis is a wall-less eubacterium belonging to the Mollicutes (trivial name, mycoplasmas) and responsible for murine respiratory diseases. The genome of strain UAB CTIP is composed of a single circular 963 879 bp chromosome with a G + C content of 26.6 mol%, i.e. the lowest reported among bacteria, Ureaplasma urealyticum apart. This genome contains 782 putative coding sequences (CDSs) covering 91.4% of its length and a function could be assigned to 486 CDSs whilst 92 matched the gene sequences of hypothetical proteins, leaving 204 CDSs without significant database match. The genome contains a single set of rRNA genes and only 29 tRNAs genes. The replication origin oriC was localized by sequence analysis and by using the G + C skew method. Sequence polymorphisms within stretches of repeated nucleotides generate phase-variable protein antigens whilst a recombinase gene is likely to catalyse the site-specific DNA inversions in major M.pulmonis surface antigens. Furthermore, a hemolysin, secreted nucleases and a glycoprotease are predicted virulence factors. Surprisingly, several of the genes previously reported to be essential for a self-replicating minimal cell are missing in the M.pulmonis genome although this one is larger than the other mycoplasma genomes fully sequenced until now.
引用
收藏
页码:2145 / 2153
页数:9
相关论文
共 65 条
[11]   Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence [J].
Cole, ST ;
Brosch, R ;
Parkhill, J ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Gordon, SV ;
Eiglmeier, K ;
Gas, S ;
Barry, CE ;
Tekaia, F ;
Badcock, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, R ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Hamlin, N ;
Holroyd, S ;
Hornby, T ;
Jagels, K ;
Krogh, A ;
McLean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Osborne, J ;
Quail, MA ;
Rajandream, MA ;
Rogers, J ;
Rutter, S ;
Seeger, K ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Taylor, K ;
Whitehead, S ;
Barrell, BG .
NATURE, 1998, 393 (6685) :537-+
[12]   Re-annotating the Mycoplasma pneumoniae genome sequence:: adding value, function and reading frames [J].
Dandekar, T ;
Huynen, M ;
Regula, JT ;
Ueberle, B ;
Zimmermann, CU ;
Andrade, MA ;
Doerks, T ;
Sánchez-Pulido, L ;
Snel, B ;
Suyama, M ;
Yuan, YP ;
Herrmann, R ;
Bork, P .
NUCLEIC ACIDS RESEARCH, 2000, 28 (17) :3278-3288
[13]   Expression, abundance, and RNA polymerase binding properties of the δ factor of Bacillus subtilis [J].
de Saro, FJL ;
Yoshikawa, N ;
Helmann, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (22) :15953-15958
[14]   DETERMINATION OF AN RNA STRUCTURE INVOLVED IN SPLICING INHIBITION OF A MUSCLE-SPECIFIC EXON [J].
DORVAL, BC ;
DAUBENTONCARAFA, Y ;
MARIE, J ;
BRODY, E .
JOURNAL OF MOLECULAR BIOLOGY, 1991, 221 (03) :837-856
[15]   Construction and use of derivatives of transposon Tn4001 that function in Mycoplasma pulmonis and Mycoplasma arthritidis [J].
Dybvig, K ;
French, CT ;
Voelker, LL .
JOURNAL OF BACTERIOLOGY, 2000, 182 (15) :4343-4347
[16]   A family of phase-variable restriction enzymes with differing specificities generated by high-frequency gene rearrangements [J].
Dybvig, K ;
Sitaraman, R ;
French, CT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (23) :13923-13928
[17]   TRANSPOSITION OF GRAM-POSITIVE TRANSPOSON TN916 IN ACHOLEPLASMA-LAIDLAWII AND MYCOPLASMA-PULMONIS [J].
DYBVIG, K ;
CASSELL, GH .
SCIENCE, 1987, 235 (4794) :1392-1394
[18]   Very fast identification of RNA motifs in genomic DNA. Application to tRNA search in the yeast genome [J].
ElMabrouk, N ;
Lisacek, F .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 264 (01) :46-55
[19]   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
[20]   Base-calling of automated sequencer traces using phred.: II.: Error probabilities [J].
Ewing, B ;
Green, P .
GENOME RESEARCH, 1998, 8 (03) :186-194