Transcriptome profiling of the C. elegans Rb ortholog reveals diverse developmental roles

被引:57
作者
Kirienko, Natalia V. [1 ]
Fay, David S. [1 ]
机构
[1] Univ Wyoming, Coll Agr, Dept Mol Biol, Dept 3944, Laramie, WY 82071 USA
关键词
lin-35; retinoblastoma; pRb; p107; p130; pocket proteins; C; elegans; development; microarray;
D O I
10.1016/j.ydbio.2007.02.021
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
LIN-35 is the single C. elegans ortholog of the mammalian pocket protein family members, pRb, p 107, and p 130. To gain insight into the roles of pocket proteins during development, a microarray analysis was performed with lin-35 mutants. Stage-specific regulation patterns were revealed, indicating that LIN-35 plays diverse roles at distinct developmental stages. LIN-35 was found to repress the expression of many genes involved in cell proliferation in larvae, an activity that is carried out in conjunction with E2F. In addition, LIN-35 was found to regulate neuronal genes during embryogenesis and targets of the intestinal-specific GATA transcription factor, ELT-2, at multiple developmental stages. Additional findings suggest that LIN-35 functions in cell cycle regulation in embryos in a manner that is independent of E2F. A comparison of LIN-35-regulated genes with known fly and mammalian pocket protein targets revealed a high degree of overlap, indicating strong conservation of pocket protein functions in diverse phyla. Based on microarray results and our refinement of the C. elegans E2F consensus sequence, we were able to generate a comprehensive list of putative E2F-regulated genes in C. elegans. These results implicate a large number of genes previously unconnected to cell cycle control as having potential roles in this process. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:674 / 684
页数:11
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