Abstract
Histone deacetylases (HDACs) are enzymes that play a pivotal role in transcription, differentiation, and cell cycle progression. We previously cloned human HDAC3 cDNA and showed that its transfection into THP-1 cells results in G2/M cell cycle accumulation. Using bioinformatic screening and PCR, we have now cloned the murine Hdac3 cDNA, which encodes a 428-amino-acid protein with near complete identity to its human ortholog. To establish a link to a potential disease locus, we performed PCR-based chromosomal mapping for the mHdac3 gene and chromosomal fluorescence in situ hybridization (FISH) for the human gene. mHdac3 localizes to chromosome 18 and human HDAC3 gene localizes to a syntenic region in chromosome 5 at band q31.3-q32 telomeric to the cytokine gene cluster. Transfection of mHdac3 into HeLa cells led to accumulation in G2/M. Our results suggest a cell cycle function for murine Hdac3, reflecting the complex regulatory roles of this gene family.
Original language | English |
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Pages (from-to) | 91-6 |
Number of pages | 6 |
Journal | Molecular cell biology research communications : MCBRC |
Volume | 2 |
Issue number | 2 |
DOIs | |
Publication status | Published - Aug 1999 |
Keywords
- Amino Acid Sequence
- Animals
- Cell Cycle
- Chromosome Mapping
- Chromosomes, Human, Pair 5
- Cloning, Molecular
- Conserved Sequence
- HeLa Cells
- Histone Deacetylases
- Humans
- In Situ Hybridization, Fluorescence
- Kidney
- Male
- Mice
- Mice, Inbred C57BL
- Molecular Sequence Data
- Polymerase Chain Reaction
- Polymorphism, Single-Stranded Conformational
- Transfection
- Journal Article
- Research Support, U.S. Gov't, P.H.S.