Sex chromosome evolution: life, death and repetitive DNA

被引:5
|
作者
Deshpande, Nikita [1 ]
Meller, Victoria H. [1 ]
机构
[1] Wayne State Univ, Dept Biol Sci, Detroit, MI 48202 USA
关键词
DOSAGE COMPENSATION; X-CHROMOSOME; DROSOPHILA-MELANOGASTER; ANALYSIS REVEALS; MSL COMPLEX; HETEROCHROMATIN; GENES;
D O I
10.1080/19336934.2015.1024395
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dimorphic sex chromosomes create problems. Males of many species, including Drosophila, are heterogametic, with dissimilar X and Y chromosomes. The essential process of dosage compensation modulates the expression of X-linked genes in one sex to maintain a constant ratio of X to autosomal expression. This involves the regulation of hundreds of dissimilar genes whose only shared property is chromosomal address. Drosophila males dosage compensate by up regulating X-linked genes 2 fold. This is achieved by the Male Specific Lethal (MSL) complex, which is recruited to genes on the X chromosome and modifies chromatin to increase expression. How the MSL complex is restricted to X-linked genes remains unknown. Recent studies of sex chromosome evolution have identified a central role for 2 types of repetitive elements in X recognition. Helitrons carrying sites that recruit the MSL complex have expanded across the X chromosome in at least one Drosophila species.1 Our laboratory found that siRNA from an X-linked satellite repeat promotes X recognition by a yet unknown mechanism.2 The recurring adoption of repetitive elements as X-identify elements suggests that the large and mysterious fraction of the genome called “junk” DNA is actually instrumental in the evolution of sex chromosomes. © 2014 Taylor & Francis Group, LLC.
引用
收藏
页码:197 / 199
页数:3
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