Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published February 6, 2020 | Supplemental Material + Accepted Version + Submitted
Journal Article Open

The SUMO Ligase Su(var)2-10 Controls Hetero- and Euchromatic Gene Expression via Establishing H3K9 Trimethylation and Negative Feedback Regulation

Abstract

Сhromatin is critical for genome compaction and gene expression. On a coarse scale, the genome is divided into euchromatin, which harbors the majority of genes and is enriched in active chromatin marks, and heterochromatin, which is gene-poor but repeat-rich. The conserved molecular hallmark of heterochromatin is the H3K9me3 modification, which is associated with gene silencing. We found that in Drosophila, deposition of most of the H3K9me3 mark depends on SUMO and the SUMO ligase Su(var)2-10, which recruits the histone methyltransferase complex SetDB1/Wde. In addition to repressing repeats, H3K9me3 influences expression of both hetero- and euchromatic host genes. High H3K9me3 levels in heterochromatin are required to suppress spurious transcription and ensure proper gene expression. In euchromatin, a set of conserved genes is repressed by Su(var)2-10/SetDB1-induced H3K9 trimethylation, ensuring tissue-specific gene expression. Several components of heterochromatin are themselves repressed by this pathway, providing a negative feedback mechanism to ensure chromatin homeostasis.

Additional Information

© 2019 Elsevier Inc. Received 13 February 2019, Revised 11 June 2019, Accepted 26 September 2019, Available online 31 December 2019. We thank members of the Fejes Tóth and Aravin labs for discussion. We are grateful to the Bloomington Stock Center and Julius Brennecke for providing flies. We thank Igor Antoshechkin (California Institute of Technology) for help with sequencing. This work was supported by grants from the National Research, Development and Innovation Office (NKFI-K117010, GINOP-2.3.2-15-2016-00032, and GINOP-2.3.2.-15-2016-00001) to (M.E. and F.J.), the NIH (R01 GM097363), the Ministry of Education and Science of the Russian Federation (14.W03.31.0007), and the Packard Fellowship Awards (to A.A.A.), and the NIH (R01GM110217) and Ellison Medical Foundation Awards (to K.F.T.). Author Contributions: M.N., A.A.A., and K.F.T. designed the experiments and wrote the manuscript. M.N., B.G., Y.L., Y.-C.A.C., and S.J.P. executed the experiments. F.J. and M.E. generated reagents. M.N. performed the computational analysis and interpretation of the data. The authors declare no competing interests.

Attached Files

Accepted Version - nihms-1548003.pdf

Submitted - 533232.full.pdf

Supplemental Material - 1-s2.0-S1097276519307592-mmc1.pdf

Files

1-s2.0-S1097276519307592-mmc1.pdf
Files (36.0 MB)
Name Size Download all
md5:cc3614b909bb2d69edc1595249427178
10.5 MB Preview Download
md5:5b7c6b6fae7bed12ee9e26b027a75864
3.8 MB Preview Download
md5:5cd4e78ff7c0e61ce1d177159dd4f7e8
21.7 MB Preview Download

Additional details

Created:
August 22, 2023
Modified:
December 22, 2023