Characterization and comparative analysis of the EGLN gene family

被引:131
作者
Taylor, MS [1 ]
机构
[1] Univ Edinburgh, Western Gen Hosp, Med Genet Sect, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
smooth muscle-20; egg laying-9; phylogeny; apoptosis; mitochondria;
D O I
10.1016/S0378-1119(01)00633-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Rat Sm-20 is a homologue of the Caenorhabditis elegans gene egl-9 and has been implicated in the regulation of growth, differentiation and apoptosis in muscle and nerve cells. Null mutants in egl-9 result in a complete tolerance to an otherwise lethal toxin produced by Pseudomonas aeruginosa. This study describes the conserved Egl-Nine (EGLN) gene family of which rat SM-20 and C. elegans Egl-9 are members and characterizes the mouse and human homologues. Each of the human genes (EGLN1, EGLN2 and EGLN3) are of a conserved genomic structure consisting of five coding exons. Phylogenetic analysis and domain organization show that EGLN1 represents the ancestral form of the gene family and that EGLN3 is the human orthologue of rat Sm-20. The previously observed mitochondrial targeting of rat SM-20 is unlikely to be a general feature of the protein family and may be a feature specific to rats. An EGLN gene is unexpectedly found in the genome of P. aeruginosa, a bacterium known to produce a toxin that acts through the Egl-9 protein. The pathogenic bacterium Vibrio cholerae is also shown to have an EGLN gene suggesting that it is an important pathogenicity factor. These results provide new insights into host-pathogen interactions and a basis for further functional characterization of the gene family and resolve discrepancies in annotation between gene family members. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:125 / 132
页数:8
相关论文
共 17 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]  
ARAVIND L, 2001, GENOME BIOL, V2
[4]   Lethal paralysis of Caenorhabditis elegans by Pseudomonas aeruginosa [J].
Darby, C ;
Cosma, CL ;
Thomas, JH ;
Manoil, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :15202-15207
[5]   Mapping, characterization, and expression analysis of the SM-20 human homologue, C1orf12, and identification of a novel related gene, SCAND2 [J].
Dupuy, D ;
Aubert, I ;
Dupérat, VG ;
Petit, J ;
Taine, L ;
Stef, M ;
Bloch, B ;
Arveiler, B .
GENOMICS, 2000, 69 (03) :348-354
[6]   Base-calling of automated sequencer traces using phred.: I.: Accuracy assessment [J].
Ewing, B ;
Hillier, L ;
Wendl, MC ;
Green, P .
GENOME RESEARCH, 1998, 8 (03) :175-185
[7]   A CYTOSOLIC PROTEIN CONTAINS A CRYPTIC MITOCHONDRIAL TARGETING SIGNAL [J].
HURT, EC ;
SCHATZ, G .
NATURE, 1987, 325 (6104) :499-503
[8]   Novel antimicrobial targets from combined pathogen and host genetics - Commentary [J].
Johnson, CD ;
Liu, LX .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (03) :958-959
[9]   Interpreting cDNA sequences: Some insights from studies on translation [J].
Kozak, M .
MAMMALIAN GENOME, 1996, 7 (08) :563-574
[10]   SM-20 is a novel mitochondrial protein that causes caspase-dependent cell death in nerve growth factor-dependent neurons [J].
Lipscomb, EA ;
Sarmiere, PD ;
Freemann, RS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (07) :5085-5092