4.7 Article

Identification of a Drosophila Myb-E2F2/RBF transcriptional repressor complex

期刊

GENES & DEVELOPMENT
卷 18, 期 23, 页码 2929-2940

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.1255204

关键词

Drosophila; transcription; Myb; E2F; RB; synMuv

资金

  1. NCI NIH HHS [CA 098131, T32 CA009041, CA 30490, R01 CA030490, P50 CA098131, R37 CA030490, CA 09041] Funding Source: Medline
  2. NHLBI NIH HHS [P01 HL068744, HL 68744] Funding Source: Medline
  3. NIAID NIH HHS [T32 AI 49824, T32 AI049824] Funding Source: Medline
  4. NIEHS NIH HHS [R01 ES011993, ES 11993] Funding Source: Medline
  5. NIGMS NIH HHS [R01 GM064779, GM 64779] Funding Source: Medline
  6. NINDS NIH HHS [R01 NS043952, NS 43952] Funding Source: Medline

向作者/读者索取更多资源

The Drosophila Myb complex has roles in both activating and repressing developmentally regulated DNA replication. To further understand biochemically the functions of the Myb complex, we fractionated Drosophila embryo extracts relying upon affinity chromatography. We found that E2F2, DP, RBF1, RBF2, and the Drosophila homolog of LIN-52, a class B synthetic multivulva (synMuv) protein, copurify with the Myb complex components to form the Myb-MuvB complex. In addition, we found that the transcriptional repressor protein, lethal (3) malignant brain tumor protein, L(3)MBT, and the histone deacetylase, Rpd3, associated with the Myb-MuvB complex. Members of the Myb-MuvB complex were localized to promoters and were shown to corepress transcription of developmentally regulated genes. These and other data now link together the Myb and E2F2 complexes in higher-order assembly to specific chromosomal sites for the regulation of transcription.

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