The Dictyostelium genome encodes numerous RasGEFs with multiple biological roles -: art. no. r68

被引:30
作者
Wilkins, A
Szafranski, K
Fraser, DJ
Bakthavatsalam, D
Müller, R
Fisher, PR
Glöckner, G
Eichinger, L
Noegel, AA
Insall, RH [1 ]
机构
[1] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
[2] Inst Mol Biotechnol, D-07745 Jena, Germany
[3] La Trobe Univ, Dept Microbiol, Melbourne, Vic 3086, Australia
[4] Univ Cologne, Fac Med, Ctr Biochem, D-50931 Cologne, Germany
[5] Univ Cologne, Fac Med, Ctr Mol Med Cologne, D-50931 Cologne, Germany
关键词
D O I
10.1186/gb-2005-6-8-r68
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Dictyostelium discoideum is a eukaryote with a simple lifestyle and a relatively small genome whose sequence has been fully determined. It is widely used for studies on cell signaling, movement and multicellular development. Ras guanine-nucleotide exchange factors (RasGEFs) are the proteins that activate Ras and thus lie near the top of many signaling pathways. They are particularly important for signaling in development and chemotaxis in many organisms, including Dictyostelium. Results: We have searched the genome for sequences encoding RasGEFs. Despite its relative simplicity, we find that the Dictyostelium genome encodes at least 25 RasGEFs, with a few other genes encoding only parts of the RasGEF consensus domains. All appear to be expressed at some point in development. The 25 genes include a wide variety of domain structures, most of which have not been seen in other organisms. The LisH domain, which is associated with microtubule binding, is seen particularly frequently; other domains that confer interactions with the cytoskeleton are also common. Disruption of a sample of the novel genes reveals that many have clear phenotypes, including altered morphology and defects in chemotaxis, slug phototaxis and thermotaxis. Conclusion: These results suggest that the unexpectedly large number of RasGEF genes reflects an evolutionary expansion of the range of Ras signaling rather than functional redundancy or the presence of multiple pseudogenes.
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页数:12
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