Repression of interrupted and intact rDNA by the SUMO pathway in Drosophila melanogaster
Abstract
Ribosomal RNAs (rRNAs) are essential components of the ribosome and are among the most abundant macromolecules in the cell. To ensure high rRNA level, eukaryotic genomes contain dozens to hundreds of rDNA genes, however, only a fraction of the rRNA genes seems to be active, while others are transcriptionally silent. We found that individual rDNA genes have high level of cell-to-cell heterogeneity in their expression in Drosophila melanogaster. Insertion of heterologous sequences into rDNA leads to repression associated with reduced expression in individual cells and decreased number of cells expressing rDNA with insertions. We found that SUMO (Small Ubiquitin-like Modifier) and SUMO ligase Ubc9 are required for efficient repression of interrupted rDNA units and variable expression of intact rDNA. Disruption of the SUMO pathway abolishes discrimination of interrupted and intact rDNAs and removes cell-to-cell heterogeneity leading to uniformly high expression of individual rDNA in single cells. Our results suggest that the SUMO pathway is responsible for both repression of interrupted units and control of intact rDNA expression.
Additional Information
© 2020 Luo et al. This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited. Received: 03 October 2019; Accepted: 06 November 2020; Published: 09 November 2020. We thank Katalin Fejes Toth and members of the Aravin lab for discussion and comments. We appreciate the help of Maayan Schwarzkopf and Niles Pierce with HCR-FISH experiments. We thank Lynn Yi for help with bioinformatics analysis. We are grateful to Michael Buszczak and the Bloomington Stock Center for providing fly stocks, Igor Dawid for providing rDNA unit constructs. We thank Igor Antoshechkin (Caltech) for help with sequencing. MN is supported by NIH/NICHD grant (K99HD099316). This work was supported by grants from the National Institutes of Health (R01 GM097363) and by the HHMI Faculty Scholar Award to AAA. TThe funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication. Author contributions: Yicheng Luo, Formal analysis, Investigation, Visualization, Writing - original draft; Elena Fefelova, Formal analysis, Investigation, Writing - original draft; Maria Ninova, Software, Formal analysis, Visualization; Yung-Chia Ariel Chen, Investigation; Alexei A Aravin, Conceptualization, Supervision, Funding acquisition, Validation, Methodology, Writing - original draft, Project administration, Writing - review and editing. Data availability: Sequencing data have been deposited in GEO under accession codes GSE141068 and GSE115277. Other data generated or analysed during this study are included in the manuscript and supporting files. The following datasets were generated: Luo Y, Fefelova E, Ninova M, Chen YA, Aravin AA. 2020. Repression of damaged and intact rDNA by the SUMO pathway. NCBI Gene Expression Omnibus. GSE141068 Ninova M, Chen YA, Godneeva B, Rogers A, Luo Y, Tóth KF, Aravin AA. 2019. The SUMO ligase Su(var)2-10 links piRNA-guided target recognition to chromatin silencing. NCBI Gene Expression Omnibus. GSE115277 The following previously published dataset was used: Gonzalez I, Mateos-Langerak J, Thomas A, Cheutin T, Cavalli G. 2014. Identification of Regulators of the Three-Dimensional Polycomb Organization by a Microscopy-Based Genome-Wide RNAi Screen. NCBI Gene Expression Omnibus. GSE55303Attached Files
Published - elife-52416-v2.pdf
Submitted - 2020.07.14.203158v1.full.pdf
Supplemental Material - elife-52416-supp-v1.zip
Supplemental Material - elife-52416-supp1-v2.docx
Supplemental Material - elife-52416-supp2-v2.docx
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Supplemental Material - elife-52416-supp5-v2.xlsx
Supplemental Material - elife-52416-transrepform-v2.pdf
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Additional details
- PMCID
- PMC7676866
- Eprint ID
- 104392
- Resolver ID
- CaltechAUTHORS:20200715-153524216
- NIH
- K99HD099316
- NIH
- R01 GM097363
- Howard Hughes Medical Institute (HHMI)
- Created
-
2020-07-15Created from EPrint's datestamp field
- Updated
-
2023-06-02Created from EPrint's last_modified field
- Caltech groups
- Division of Biology and Biological Engineering (BBE)