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.
journal_name
Geneticsjournal_title
Geneticsauthors
Beckstead RB,Ner SS,Hales KG,Grigliatti TA,Baker BS,Bellen HJdoi
10.1534/genetics.104.037085keywords:
subject
Has Abstractpub_date
2005-02-01 00:00:00pages
783-94issue
2eissn
0016-6731issn
1943-2631pii
genetics.104.037085journal_volume
169pub_type
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