MLL1/WDR5 complex in leukemogenesis and epigenetic regulation
MLL1 is a histone H3Lys4 methyltransferase and forms a complex with WDR5 and other components. It plays important roles in developmental events, transcriptional regulation, and leukemogenesis. MLL1-fusion proteins resulting from chromosomal translocations are molecular hallmarks of a special type of...
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Published in | Ai zheng Vol. 30; no. 4; pp. 240 - 246 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
College of Life Sciences, Wuhan University, Wuhan,Hubei 430072, P. R. China
01.04.2011
Sun Yat-sen University Cancer Center |
Subjects | |
Online Access | Get full text |
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Summary: | MLL1 is a histone H3Lys4 methyltransferase and forms a complex with WDR5 and other components. It plays important roles in developmental events, transcriptional regulation, and leukemogenesis. MLL1-fusion proteins resulting from chromosomal translocations are molecular hallmarks of a special type of leukemia, which occurs in over 70% infant leukemia patients and often accompanies poor prognosis. Investigations in the past years on leukemogenesis and the MLLI-WDR5 histone H3Lys4 methyltransferase complex demonstrate that epigenetic regulation is one of the key steps in development and human diseases. |
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Bibliography: | MLL1 is a histone H3Lys4 methyltransferase and forms a complex with WDR5 and other components. It plays important roles in developmental events, transcriptional regulation, and leukemogenesis. MLL1-fusion proteins resulting from chromosomal translocations are molecular hallmarks of a special type of leukemia, which occurs in over 70% infant leukemia patients and often accompanies poor prognosis. Investigations in the past years on leukemogenesis and the MLLI-WDR5 histone H3Lys4 methyltransferase complex demonstrate that epigenetic regulation is one of the key steps in development and human diseases. 44-1195/R MLL1, WDR5, leukemia, epigenetic regulation, signal transduction ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 1000-467X 1944-446X |
DOI: | 10.5732/cjc.011.10055 |