Systematic Analysis of SIN3 Histone Modifying Complex Components During Development

• Published in: Scientific reports Vol. 8; no. 1; pp. 17048 - 11
• Main Authors: Barnes, Valerie L., Laity, Kelly A., Pilecki, Maksymilian, Pile, Lori A.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 19.11.2018; Nature Publishing Group
• Subjects: 13/51; 38; 38/89; 631/208/135; 631/337/100/2285; 64; 64/24; Acetylation; Animals; Apoptosis; Cell growth; Cell Proliferation; Cell Survival; Chromosomes; Deacetylation; Drosophila; Drosophila melanogaster; Drosophila Proteins - metabolism; Female; Histone deacetylase; Histones - metabolism; Humanities and Social Sciences; Insects; Lethality; Male; Molecular modelling; multidisciplinary; Phenotypes; Polytene; Polytene chromosomes; Science; Science (multidisciplinary); Sin3 Histone Deacetylase and Corepressor Complex - metabolism; Sin Binding; Polytene Chromosome Preparations; RNAi Knockdown; Wing Imaginal Disc; Sin3 Complex
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-35093-0

Establishment and maintenance of histone acetylation levels are critical for metazoan development and viability. Disruption of the balance between acetylation and deacetylation by treatment with chemical histone deacetylase (HDAC) inhibitors results in loss of cell proliferation, differentiation and/or apoptosis. Histone deacetylation by the SIN3 complex is essential in Drosophila and mice, as loss of the scaffolding factor SIN3 or the associated HDAC results in lethality. The objective of this study is to elucidate contributions of SIN3 complex components to these essential processes. We used the Drosophila model organism to carry out a systematic functional analysis of the SIN3 complex. We find that SIN3 associated proteins are essential for viability and cell proliferation during development. Additionally, tissue specific reduction of SIN3 complex components results in abnormal wing development. Interestingly, while knockdown of each factor resulted in similar phenotypes, their individual effects on recruitment of SIN3 to polytene chromosomes are distinct. Reduction of some factors leads to large changes in the morphology of the chromosome and/or greatly reduced SIN3 binding. These findings suggest that while individual SIN3 complex components work through distinct molecular mechanisms, they each make a substantial contribution to the overall function of this highly conserved histone deacetylase complex.