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Publication : MLL, a mammalian trithorax-group gene, functions as a transcriptional maintenance factor in morphogenesis.

First Author  Yu BD Year  1998
Journal  Proc Natl Acad Sci U S A Volume  95
Issue  18 Pages  10632-6
PubMed ID  9724755 Mgi Jnum  J:49977
Mgi Id  MGI:1289645 Doi  10.1073/pnas.95.18.10632
Citation  Yu BD, et al. (1998) MLL, a mammalian trithorax-group gene, functions as a transcriptional maintenance factor in morphogenesis. Proc Natl Acad Sci U S A 95(18):10632-6
abstractText  Determinative events in vertebrate embryogenesis appear to require the continuous expression of spatial regulators such as the clustered homeobox genes. The mechanisms that govern long-term patterns of gene expression are not well understood. In Drosophila, active and silent states of developmentally regulated loci are maintained by trithorax and Polycomb group. We have examined the developmental role of a mammalian homolog of trx and putative oncogene, Mll. Knockout mice reveal that Mll is required for maintenance of gene expression early in embryogenesis. Downstream targets of Mll including Hoxa7 are activated appropriately in the absence of Mll but require Mll for sustaining their expression. The Mll-/- phenotype manifests later in development and is characterized by branchial arch dysplasia and aberrant segmental boundaries of spinal ganglia and somites. Thus, Mll represents an essential mechanism of transcriptional maintenance in mammalian development, which functions in multiple morphogenetic processes.
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