Comparative genomics of gene expression in the parasitic and free-living nematodes Strongyloides stercoralis and Caenorhabditis elegans

被引:73
作者
Mitreva, M [1 ]
McCarter, JP
Martin, J
Dante, M
Wylie, T
Chiapelli, B
Pape, D
Clifton, SW
Nutman, TB
Waterston, RH
机构
[1] Washington Univ, Sch Med, Genome Sequencing Ctr, St Louis, MO 63108 USA
[2] Divergence Inc, St Louis, MO 63141 USA
[3] NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[4] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
关键词
D O I
10.1101/gr.1524804
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 developmental timing of gene expression is used to infer potential gene function, Studies have yet to correlate this information between species. We analyzed 10,921 ESTs in 3311 clusters from first- and infective third-stage larva (L1, L3i) of the parasitic nematode Strongyloides stercoralis and compared the results to Caenorhabditis elegans, a species that has an L3i-like dauer stage. In the comparison of S. stercoralis clusters with stage-specific expression to C elegans homologs expressed in either dauer or nondauer stages, matches between S. stercoralis L1 and C elegans nondauer-expressed genes dominated, suggesting conservation in the repertoire of genes expressed during growth in nutrient-rich conditions. For example, S. stercoralis collagen transcripts were abundant in L1 but not L3i, a pattern consistent with C elegans collagens. Although a greater proportion of S. stercoralis L3i than L1 genes have homologs among the C elegans dauer-specific transcripts, we did not uncover evidence of a robust conserved L3i/dauer 'expression signature.' Strikingly, in comparisons of S. stercoralis clusters to C elegans homologs with RNAi knockouts, those with significant L1-specific expression were more than twice as likely as L3i-specific clusters to match genes with phenotypes. We also provide functional classifications of S. stercoralis clusters.
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页码:209 / 220
页数:12
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共 90 条
[11]   Reconstruction of amino acid biosynthesis pathways from the complete genome sequence [J].
Bono, H ;
Ogata, H ;
Goto, S ;
Kanehisa, M .
GENOME RESEARCH, 1998, 8 (03) :203-210
[12]   Genome evolution and developmental constraint in Caenorhabditis elegans [J].
Castillo-Davis, CI ;
Hartl, DL .
MOLECULAR BIOLOGY AND EVOLUTION, 2002, 19 (05) :728-735
[13]   DUODENAL STRONGYLOIDES-STERCORALIS INFECTION [J].
CHEN, JJ ;
LEE, CM ;
CHANGCHAN, CS .
ENDOSCOPY, 1994, 26 (02) :272-272
[14]   Expression of the microfilarial sheath protein 2 (shp2) of the filarial parasites Litomosoides sigmodontis and Brugia malayi [J].
Conraths, FJ ;
Hirzmann, J ;
Hobom, G ;
Zahner, H .
EXPERIMENTAL PARASITOLOGY, 1997, 85 (03) :241-248
[15]   MOLECULAR AND BIOCHEMICAL ASPECTS OF NEMATODE COLLAGENS [J].
COX, GN .
JOURNAL OF PARASITOLOGY, 1992, 78 (01) :1-15
[16]   A survey of genes expressed in adults of the human hookworm, Necator americanus [J].
Daub, J ;
Loukas, A ;
Pritchard, DI ;
Blaxter, M .
PARASITOLOGY, 2000, 120 :171-184
[17]   Single pass cDNA sequencing -: a powerful tool to analyse gene expression in preparasitic juveniles of the southern root-knot nematode Meloidogyne incognita [J].
Dautova, M ;
Rosso, MN ;
Abad, P ;
Gommers, FJ ;
Bakker, J ;
Smant, G .
NEMATOLOGY, 2001, 3 :129-139
[18]   Molecular cloning and characterisation of a venom allergen AG5-like cDNA from Meloidogyne incognita [J].
Ding, X ;
Shields, J ;
Allen, R ;
Hussey, RS .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2000, 30 (01) :77-81
[19]   A CLONED ANTIGEN FOR SEROLOGICAL DIAGNOSIS OF WUCHERERIA-BANCROFTI MICROFILAREMIA WITH DAYTIME BLOOD-SAMPLES [J].
DISSANAYAKE, S ;
XU, M ;
PIESSENS, WF .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1992, 56 (02) :269-277
[20]   EVALUATION OF A RECOMBINANT PARASITE ANTIGEN FOR THE DIAGNOSIS OF LYMPHATIC FILARIASIS [J].
DISSANAYAKE, S ;
ZHENG, HJ ;
DREYER, G ;
XU, M ;
WATAWANA, L ;
CHENG, GH ;
WANG, SH ;
MORIN, P ;
DENG, BJ ;
KURNIAWAN, L ;
VINCENT, A ;
PIESSENS, WF .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1994, 50 (06) :727-734