| Literature DB >> 15545640 |
R B Beckstead1, S S Ner, K G Hales, T A Grigliatti, B S Baker, H J Bellen.
Abstract
Bonus, a Drosophila TIF1 homolog, is a nuclear receptor cofactor required for viability, molting, and numerous morphological events. Here we establish a role for Bonus in the modulation of chromatin structure. We show that weak loss-of-function alleles of bonus have a more deleterious effect on males than on females. This male-enhanced lethality is not due to a defect in dosage compensation or somatic sex differentiation, but to the presence of the Y chromosome. Additionally, we show that bonus acts as both an enhancer and a suppressor of position-effect variegation. By immunostaining, we demonstrate that Bonus is associated with both interphase and prophase chromosomes and through chromatin immunoprecipitation show that two of these sites correspond to the histone gene cluster and the Stellate locus.Entities:
Keywords: NASA Discipline Developmental Biology; Non-NASA Center
Mesh:
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Year: 2004 PMID: 15545640 PMCID: PMC1449102 DOI: 10.1534/genetics.104.037085
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562