Examining the function and mechanism of histone variant H2A.z (HTZ-1) in transcriptional repression.

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2020-05

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The Ohio State University

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Abstract

Proper gene regulation is vital for development and cell differentiation and one method in which cells regulate genes is via chromatin structure. Histones play an important role in determining chromatin structure and that chromatin structure can influence if a gene is active or inactive. In C. elegans, Myb-MuvB/DREAM complex proteins manage inappropriate transcript accumulation by transcriptionally repressing target genes through depositing the histone variant H2A.z/HTZ-1 along the gene body. Here, we studied the in vivo characteristics of H2A.z/HTZ-1 mutants and compared them to the known characteristics of Myb-MuvB/DREAM complex mutants. Similar phenotypes suggested that H2A.z/HTZ-1 behaves similarly to and can be classified as a Myb-MuvB/DREAM complex protein. Additionally, we proposed that H2A./HTZ-1 functions in this gene repression pathway to directly condense and close the chromatin state. We also showed that H2A.z/HTZ-1 gene repression function is conserved between organisms by studying characteristics in a different nematode, C. briggsae. Studying H2A.z/HTZ-1 associated gene repression is important because H2A.z/HTZ-1 has also been tied to gene activation. A better understanding of exactly how H2A.z/HTZ-1 functions can provide valuable insight into gene regulation.

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Denman Undergraduate Research Forum Finalist in Genetics and Cancer (2020)

Keywords

genetics, DNA, histones, cancer, gene regulation, C. elegans

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