The complete genome and proteome of Mycoplasma mobile

被引:195
作者
Jaffe, JD
Stange-Thomann, N
Smith, C
DeCaprio, D
Fisher, S
Butler, J
Calvo, S
Elkins, T
Fitzgerald, MG
Hafez, N
Kodira, CD
Major, J
Wang, SG
Wilkinson, J
Nicol, R
Nusbaum, C
Birren, B
Berg, HC
Church, GM [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[3] Harvard Univ, Broad Inst, Cambridge, MA 02141 USA
[4] MIT, Broad Inst, Cambridge, MA 02141 USA
[5] Harvard Univ, Rowland Inst, Cambridge, MA 02141 USA
关键词
D O I
10.1101/gr.2674004
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
Although often considered "minimal" organisms, mycoplasmas show a wide range of diversity with respect to host environment, phenotypic traits, and pathogenicity. Here we report the complete genomic sequence and proteogenomic map for the piscine mycoplasma Mycoplasma mobile, noted for its robust gliding motility. For the first time, proteomic data are used in the primary annotation of a new genome, providing validation of expression for many of the predicted proteins. Several novel features were discovered including along repeating unit of DNA of similar to2435 by present in five complete copies that are shown to code for nearly identical yet uniquely expressed proteins. M. mobile has among the lowest DNA GC contents (24.9%) and most reduced set of tRNAs of any organism yet reported (28). Numerous instances of tandem duplication as well as lateral gene transfer are evident in the genome. The multiple available complete genome sequences for other motile and immotile mycoplasmas enabled us to use comparative genomic and phylogenetic methods to suggest several candidate genes that might be involved in motility. The results of these analyses leave open the possibility that gliding motility might have arisen independently more than once in the mycoplasma lineage.
引用
收藏
页码:1447 / 1461
页数:15
相关论文
共 70 条
[21]   Complete sequence analysis of the genome of the bacterium Mycoplasma pneumoniae [J].
Himmelreich, R ;
Hilbert, H ;
Plagens, H ;
Pirkl, E ;
Li, BC ;
Herrmann, R .
NUCLEIC ACIDS RESEARCH, 1996, 24 (22) :4420-4449
[22]  
HOFMANN K, 1993, BIOL CHEM HOPPESEYLE, V364, P166
[23]   The junctional pore complex, a prokaryotic secretion organelle, is the molecular motor underlying gliding motility in cyanobacteria [J].
Hoiczyk, E ;
Baumeister, W .
CURRENT BIOLOGY, 1998, 8 (21) :1161-1168
[24]   A MYCOPLASMA-GENITALIUM PROTEIN RESEMBLING THE MYCOPLASMA-PNEUMONIAE ATTACHMENT PROTEIN [J].
HU, PC ;
SCHAPER, U ;
COLLIER, AM ;
CLYDE, WA ;
HORIKAWA, M ;
HUANG, YS ;
BARILE, MF .
INFECTION AND IMMUNITY, 1987, 55 (05) :1126-1131
[25]   Whole-genome sequence assembly for mammalian genomes: Arachne 2 [J].
Jaffe, DB ;
Butler, J ;
Gnerre, S ;
Mauceli, E ;
Lindblad-Toh, K ;
Mesirov, JP ;
Zody, MC ;
Lander, ES .
GENOME RESEARCH, 2003, 13 (01) :91-96
[26]   Energetics of gliding motility in Mycoplasma mobile [J].
Jaffe, JD ;
Miyata, M ;
Berg, HC .
JOURNAL OF BACTERIOLOGY, 2004, 186 (13) :4254-4261
[27]   Proteogenomic mapping as a complementary method to perform genome annotation [J].
Jaffe, JD ;
Berg, HC ;
Church, GM .
PROTEOMICS, 2004, 4 (01) :59-77
[28]  
Karp Peter D, 2002, Bioinformatics, V18 Suppl 1, pS225
[29]   Identification of a new variable sequence in the P1 cytadhesin gene of Mycoplasma pneumoniae:: Evidence for the generation of antigenic variation by DNA recombination between repetitive sequences [J].
Kenri, T ;
Taniguchi, R ;
Sasaki, Y ;
Okazaki, N ;
Narita, M ;
Izumikawa, K ;
Umetsu, M ;
Sasaki, T .
INFECTION AND IMMUNITY, 1999, 67 (09) :4557-4562
[30]  
KIRCHHOFF H, 1984, J GEN MICROBIOL, V130, P2439