A revised annotation and comparative analysis of Helicobacter pylori genomes

被引:59
作者
Boneca, IG [1 ]
de Reuse, H
Epinat, JC
Pupin, M
Labigne, A
Moszer, I
机构
[1] Inst Pasteur, Unite Pathogenie Bacterienne Muqueuses, Paris, France
[2] Inst Pasteur, Unite Genet Genomes Bacteriens, Paris, France
关键词
D O I
10.1093/nar/gkg250
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
Huge amounts of genomic information are currently being generated. Therefore, biologists require structured, exhaustive and comparative databases. The PyloriGene database (http://genolist.pasteur.fr/PyloriGene) was developed to respond to these needs, by integrating and connecting the information generated during the sequencing of two distinct strains of Helicobacter pylori. This led to the need for a general annotation consensus, as the physical and functional annotations of the two strains differed significantly in some cases. A revised functional classification system was created to accommodate the existing data and to make it possible to classify coding sequences (CDS) into several functional categories to harmonize CDS classification. The annotation of the two complete genomes was revised in the light of new data, allowing us to reduce the percentage of hypothetical proteins from similar to40 to 33%. This resulted in the reassignment of functions for 108 CDS (similar to7% of all CDS). Interestingly, the functions of only similar to13% of CDS (222 out of 1658 CDS) were annotated as a result of work done directly on H.pylori genes. Finally, comparison of the two published genomes revealed a significant amount of size variation between corresponding (orthologous) CDS. Most of these size variations were due to natural polymorphisms, although other sources of variation were identified, such as pseudogenes, new genes potentially regulated by slipped-strand mispairing mechanism, or frame-shifts. 113 of these differences were due to different start codon assignments, a common problem when constructing physical annotations.
引用
收藏
页码:1704 / 1714
页数:11
相关论文
共 78 条
[1]   Genomic-sequence comparison of two unrelated isolates of the human gastric pathogen Helicobacter pylori [J].
Alm, RA ;
Ling, LSL ;
Moir, DT ;
King, BL ;
Brown, ED ;
Doig, PC ;
Smith, DR ;
Noonan, B ;
Guild, BC ;
deJonge, BL ;
Carmel, G ;
Tummino, PJ ;
Caruso, A ;
Uria-Nickelsen, M ;
Mills, DM ;
Ives, C ;
Gibson, R ;
Merberg, D ;
Mills, SD ;
Jiang, Q ;
Taylor, DE ;
Vovis, GF ;
Trost, TJ .
NATURE, 1999, 397 (6715) :176-180
[2]   Comparative genomics of Helicobacter pylori:: Analysis of the outer membrane protein families [J].
Alm, RA ;
Bina, J ;
Andrews, BM ;
Doig, P ;
Hancock, REW ;
Trust, TJ .
INFECTION AND IMMUNITY, 2000, 68 (07) :4155-4168
[3]   Analysis of the genetic diversity of Helicobacter pylori:: the tale of two genomes [J].
Alm, RA ;
Trust, TJ .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1999, 77 (12) :834-846
[4]   LytB, a novel gene of the 2-C-methyl-D-erythritol 4-phosphate pathway of isoprenoid biosynthesis in Escherichia coli [J].
Altincicek, B ;
Kollas, AK ;
Eberl, M ;
Wiesner, J ;
Sanderbrand, S ;
Hintz, M ;
Beck, E ;
Jomma, H .
FEBS LETTERS, 2001, 499 (1-2) :37-40
[5]   GcpE is involved in the 2-C-methyl-D-erythritol 4-phosphate pathway of isoprenoid biosynthesis in Escherichia coli [J].
Altincicek, B ;
Kollas, AK ;
Sanderbrand, S ;
Wiesner, J ;
Hintz, M ;
Beck, E ;
Jomaa, H .
JOURNAL OF BACTERIOLOGY, 2001, 183 (08) :2411-2416
[6]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[7]   HP0333, a member of the dprA family, is involved in natural transformation in Helicobacter pylori [J].
Ando, T ;
Israel, DA ;
Kusugami, K ;
Blaser, MJ .
JOURNAL OF BACTERIOLOGY, 1999, 181 (18) :5572-5580
[8]   Phase variation in H type I and Lewis a epitopes of Helicobacter pylori lipopolysaccharide [J].
Appelmelk, BJ ;
Martino, MC ;
Veenhof, E ;
Monteiro, MA ;
Maaskant, JJ ;
Negrini, R ;
Lindh, F ;
Perry, M ;
Del Giudice, G ;
Vandenbroucke-Grauls, CMJE .
INFECTION AND IMMUNITY, 2000, 68 (10) :5928-5932
[9]   Phase variation in Helicobacter pylori lipopolysaccharide due to changes in the lengths of poly(C) tracts in α3-fucosyltransferase genes [J].
Appelmelk, BJ ;
Martin, SL ;
Monteiro, MA ;
Clayton, CA ;
McColm, AA ;
Zheng, PY ;
Verboom, T ;
Maaskant, JJ ;
Van den Eijnden, DH ;
Hokke, CH ;
Perry, MB ;
Vandenbroucke-Grauls, CMJE ;
Kusters, JG .
INFECTION AND IMMUNITY, 1999, 67 (10) :5361-5366
[10]   MOSAICISM IN VACUOLATING CYTOTOXIN ALLELES OF HELICOBACTER-PYLORI - ASSOCIATION OF SPECIFIC VACA TYPES WITH CYTOTOXIN PRODUCTION AND PEPTIC-ULCERATION [J].
ATHERTON, JC ;
CAO, P ;
PEEK, RM ;
TUMMURU, MKR ;
BLASER, MJ ;
COVER, TL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (30) :17771-17777