Abstract
Two overlapping cDNAs that encode a 197-kDa sequence-selective DNA-binding protein were isolated from libraries derived from mouse lymphoid cell mRNA. In addition to a DNA-binding domain, the protein contains both a chromodomain, which occurs in proteins that are implicated in chromatin compaction, and an SNF2/SWI2-like helicase domain, which occurs in proteins that are believed to activate transcription by counteracting the repressive effects of chromatin structure. A Southern blot analysis indicated that this protein, which we have named CHD-1, for chromodomain-helicase-DNA-binding protein, is present in most, if not all, mammalian species. A Northern blot analysis revealed multiple CHD mRNA components that differed both qualitatively and quantitatively among various cell types. The various mRNAs, which are probably produced by alternative RNA processing, could conceivably encode tissue-specific and developmental stage-specific isoforms of the protein. Based on its interesting combination of features, we suspect that CHD-1 plays an important role in gene regulation.
MeSH Terms
Amino Acid Sequence
Animals
Base Sequence
Blotting, Northern
DNA Helicases/genetics
DNA-Binding Proteins/genetics
Fungal Proteins/genetics
Gene Library
Humans
Lymphoma, B-Cell
Mice
Molecular Sequence Data
Nuclear Proteins
RNA, Messenger/genetics,isolation & purification
Sequence Homology, Amino Acid
Transcription Factors/genetics
Tumor Cells, Cultured
Chemicals
Chd1 protein, mouse
DNA-Binding Proteins
Fungal Proteins
Nuclear Proteins
RNA, Messenger
SMARCA1 protein, human
SMARCA2 protein, human
Smarca2 protein, mouse
Transcription Factors
SMARCA4 protein, human
Smarca4 protein, mouse
DNA Helicases
CHD1 protein, human
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Delmas V
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111.
Stokes D G
Perry R P
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