| Literature DB >> 29668306 |
Maria Samata1,2, Asifa Akhtar1.
Abstract
X chromosome regulation represents a prime example of an epigenetic phenomenon where coordinated regulation of a whole chromosome is required. In flies, this is achieved by transcriptional upregulation of X chromosomal genes in males to equalize the gene dosage differences in females. Chromatin-bound proteins and long noncoding RNAs (lncRNAs) constituting a ribonucleoprotein complex known as the male-specific lethal (MSL) complex or the dosage compensation complex mediate this process. MSL complex members decorate the male X chromosome, and their absence leads to male lethality. The male X chromosome is also enriched with histone H4 lysine 16 acetylation (H4K16ac), indicating that the chromatin compaction status of the X chromosome also plays an important role in transcriptional activation. How the X chromosome is specifically targeted and how dosage compensation is mechanistically achieved are central questions for the field. Here, we review recent advances, which reveal a complex interplay among lncRNAs, the chromatin landscape, transcription, and chromosome conformation that fine-tune X chromosome gene expression.Entities:
Keywords: H4K16ac; X chromosome; dosage compensation; histone acetylation; long noncoding RNAs; male-specific lethal; transcription
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Year: 2018 PMID: 29668306 DOI: 10.1146/annurev-biochem-062917-011816
Source DB: PubMed Journal: Annu Rev Biochem ISSN: 0066-4154 Impact factor: 23.643