E2F-8: an E2F family member with a similar organization of DNA-binding domains to E2F-7
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机构:
Nicola Logan
Anne Graham
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机构:University of Glasgow,Division of Biochemistry and Molecular Biology
Anne Graham
Xuijie Zhao
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机构:University of Glasgow,Division of Biochemistry and Molecular Biology
Xuijie Zhao
Rebecca Fisher
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机构:University of Glasgow,Division of Biochemistry and Molecular Biology
Rebecca Fisher
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Baidehi Maiti
Gustavo Leone
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机构:University of Glasgow,Division of Biochemistry and Molecular Biology
Gustavo Leone
Nicholas B La Thangue
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机构:University of Glasgow,Division of Biochemistry and Molecular Biology
Nicholas B La Thangue
机构:
[1] University of Glasgow,Division of Biochemistry and Molecular Biology
[2] Human Cancer Genetics Program,Department of Molecular Virology
[3] Immunology and Medical Genetics,undefined
[4] The Ohio State University,undefined
来源:
Oncogene
|
2005年
/
24卷
关键词:
E2F;
cancer;
cell cycle;
transcription factor;
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摘要:
E2F is a family of transcription factors implicated in cell cycle control. To understand the role of E2F in controlling cell cycle progression, it is necessary to clarify the breadth of the E2F family. To date, seven E2F subunits have been identified. We report here the characterization of a new E2F subunit, E2F-8, which resembles the organization of E2F-7 in the presence of two separate DNA-binding domains, the integrity of which is required for E2F-8 to bind to DNA. Furthermore, like E2F-7, we find that E2F-8 can repress transcription and delay cell cycle progression. The similarities between E2F-7 and E2F-8 define a new subgroup of the E2F family, and further imply that E2F-7 and E2F-8 may act through overlapping mechanisms in mediating cell cycle control.