Dissecting Nucleosome Function with a Comprehensive Histone H2A and H2B Mutant Library

Author:

Jiang Shuangying123,Liu Yan12,Xu Caiyue12,Wang Yun45,Gong Jianhui45,Shen Yue45,Wu Qingyu12,Boeke Jef D67,Dai Junbiao123

Affiliation:

1. Ministry of Education Key Laboratory of Bioinformatics, School of Life Sciences, Tsinghua University, Beijing 100084, PR China

2. Center for Synthetic and Systems Biology, School of Life Sciences, Tsinghua University, Beijing 100084, PR China

3. Center for Synthetic Biology Engineering Research, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China

4. China National GeneBank, Beijing Genomics Institute-Shenzhen, Shenzhen 518120, China

5. Beijing Genomics Institute-Shenzhen, Shenzhen 518083, China

6. Institute for Systems Genetics, New York University Langone Medical Center, New York 10011

7. Department of Biochemistry and Molecular Pharmacology, New York University Langone Medical Center, New York 10011

Abstract

Abstract Using a comprehensive library of histone H2A and H2B mutants, we assessed the biological function of each amino acid residue involved in various stress conditions including exposure to different DNA damage-inducing reagents, different growth temperatures, and other chemicals. H2B N- and H2A C-termini were critical for maintaining nucleosome function and mutations in these regions led to pleiotropic phenotypes. Additionally, two screens were performed using this library, monitoring heterochromatin gene silencing and genome stability, to identify residues that could compromise normal function when mutated. Many distinctive regions within the nucleosome were revealed. Furthermore, we used the barcode sequencing (bar-seq) method to profile the mutant composition of many libraries in one high-throughput sequencing experiment, greatly reducing the labor and increasing the capacity. This study not only demonstrates the applications of the versatile histone library, but also reveals many previously unknown functions of histone H2A and H2B.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

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