Menin localizes to chromatin through an ATR-CHK1 mediated pathway after UV-induced DNA damage (Q24337033)

GOA release 2020-03-11

author name string

Steven M Farley

1

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Gao Chen

2

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Sydney Guo

3

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Min Wang

4

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Jingbo A

5

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Felix Lee

6

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Frank Lee

7

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Mark Sawicki

Journal of Surgical Research

8

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language of work or name

English

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publication date

1 June 2006

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published in

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volume

133

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issue

1

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page(s)

29-37

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cites work

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The menin tumor suppressor protein is an essential oncogenic cofactor for MLL-associated leukemogenesis

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Chk1 in the DNA damage response: conserved roles from yeasts to mammals

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Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription

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Menin associates with a trithorax family histone methyltransferase complex and with the hoxc8 locus

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Quantitation and visualization of ultraviolet-induced DNA damage using specific antibodies: application to pigment cell biology

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The tumor suppressor protein menin interacts with NF-kappaB proteins and inhibits NF-kappaB-mediated transactivation

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Menin and MLL cooperatively regulate expression of cyclin-dependent kinase inhibitors

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Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type beta signaling

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A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors

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Expression of wild-type p53 is required for efficient global genomic nucleotide excision repair in UV-irradiated human fibroblasts

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Inactivation of menin, the product of the multiple endocrine neoplasia type 1 gene, inhibits the commitment of multipotential mesenchymal stem cells into the osteoblast lineage

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In vivo recruitment of XPC to UV-induced cyclobutane pyrimidine dimers by the DDB2 gene product

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Menin induces apoptosis in murine embryonic fibroblasts

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Differential mode of regulation of the checkpoint kinases CHK1 and CHK2 by their regulatory domains

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Menin is required for bone morphogenetic protein 2- and transforming growth factor beta-regulated osteoblastic differentiation through interaction with Smads and Runx2

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Reduction of menin expression enhances cell proliferation and is tumorigenic in intestinal epithelial cells

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Direct binding of DNA by tumor suppressor menin

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Core filaments of the nuclear matrix

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The 32-kilodalton subunit of replication protein A interacts with menin, the product of the MEN1 tumor suppressor gene

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Leukemia proto-oncoprotein MLL forms a SET1-like histone methyltransferase complex with menin to regulate Hox gene expression

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Functional interaction between tumor suppressor menin and activator of S-phase kinase

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