Literature DB >> 9712723

Cloning, chromosome mapping and expression analysis of the HIRA gene from Drosophila melanogaster.

R Llevadot1, G Marqués, M Pritchard, X Estivill, A Ferrús, P Scambler.   

Abstract

The human HIRA gene was identified as a putative transcriptional regulator mapping within the DiGeorge syndrome critical region at 22q11. HIRA-related proteins have been described in a number of species, but functional information concerning family members is only available in Saccharomyces cerevisiae, where the Hir1p and Hir2p proteins are known to be transcriptional corepressors. In order to analyse conservation of HIRA-related genes and to provide resources for functional studies in another model organism we have isolated the HIRA gene from Drosophila melanogaster (dhira). The 3374 nucleotide cDNA encodes a protein of 1047 aa, showing 42% identity with the human protein. Alignment with the predicted HIRA proteins from human, mouse, chick and pufferfish reveals strong conservation within the N-terminal region which contains seven WD domains, with less conservation of C-terminal sequences. In situ hybridisation to salivary gland chromosomes indicates that the gene resides in region 7B2-3 of the X chromosome. Dhira is expressed through embryonic development and at lower levels during larval and pupal development. The expression of dhira is dramatically increased in early embryos and in females, suggesting that the dhira mRNA could be maternally deposited in the embryos. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9712723     DOI: 10.1006/bbrc.1998.9165

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  6 in total

1.  HIRA, the human homologue of yeast Hir1p and Hir2p, is a novel cyclin-cdk2 substrate whose expression blocks S-phase progression.

Authors:  C Hall; D M Nelson; X Ye; K Baker; J A DeCaprio; S Seeholzer; M Lipinski; P D Adams
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

2.  Targeted mutagenesis of the Hira gene results in gastrulation defects and patterning abnormalities of mesoendodermal derivatives prior to early embryonic lethality.

Authors:  Catherine Roberts; Helen F Sutherland; Hannah Farmer; Wendy Kimber; Stephanie Halford; Alisoun Carey; Joshua M Brickman; Anthony Wynshaw-Boris; Peter J Scambler
Journal:  Mol Cell Biol       Date:  2002-04       Impact factor: 4.272

Review 3.  Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development.

Authors:  Daniel W Meechan; Thomas M Maynard; Eric S Tucker; Alejandra Fernandez; Beverly A Karpinski; Lawrence A Rothblat; Anthony-S LaMantia
Journal:  Prog Neurobiol       Date:  2015-04-09       Impact factor: 11.685

4.  Separation-of-function mutation in HPC2, a member of the HIR complex in S. cerevisiae, results in derepression of the histone genes but does not confer cryptic TATA phenotypes.

Authors:  Nidhi Vishnoi; Kacie Flaherty; Leandria C Hancock; Monica E Ferreira; Amit Dipak Amin; Philippe Prochasson
Journal:  Biochim Biophys Acta       Date:  2011-07-19

5.  HIRA is essential for the development of gibel carp.

Authors:  Meng-Yu Wang; Qiu-Hong Guo; Xin-Zheng Du; Li Zhou; Qian Luo; Qiao-Hui Zeng; Jia-Lin Wang; Hao-Bin Zhao; Yu-Feng Wang
Journal:  Fish Physiol Biochem       Date:  2013-08-04       Impact factor: 2.794

6.  The essential role of Drosophila HIRA for de novo assembly of paternal chromatin at fertilization.

Authors:  Emilie Bonnefoy; Guillermo A Orsi; Pierre Couble; Benjamin Loppin
Journal:  PLoS Genet       Date:  2007-09-10       Impact factor: 5.917

  6 in total

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