Transcription of a 5’ extended mRNA isoform directs dynamic chromatin changes and interference of a downstream promoter

Author:

Chia Minghao1,Tresenrider Amy2,Chen Jingxun2,Spedale Gianpiero1,Jorgensen Victoria2,Ünal Elçin2,van Werven Folkert Jacobus1ORCID

Affiliation:

1. The Francis Crick Institute, London, United Kingdom

2. Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States

Abstract

Cell differentiation programs require dynamic regulation of gene expression. During meiotic prophase in Saccharomyces cerevisiae, expression of the kinetochore complex subunit Ndc80 is downregulated by a 5’ extended long undecoded NDC80 transcript isoform. Here we demonstrate a transcriptional interference mechanism that is responsible for inhibiting expression of the coding NDC80 mRNA isoform. Transcription from a distal NDC80 promoter directs Set1-dependent histone H3K4 dimethylation and Set2-dependent H3K36 trimethylation to establish a repressive chromatin state in the downstream canonical NDC80 promoter. As a consequence, NDC80 expression is repressed during meiotic prophase. The transcriptional mechanism described here is rapidly reversible, adaptable to fine-tune gene expression, and relies on Set2 and the Set3 histone deacetylase complex. Thus, expression of a 5’ extended mRNA isoform causes transcriptional interference at the downstream promoter. We demonstrate that this is an effective mechanism to promote dynamic changes in gene expression during cell differentiation.

Funder

Francis Crick Institute

Pew Charitable Trusts

Glenn Foundation for Medical Research

March of Dimes Foundation

National Science Foundation

Agency for Science, Technology and Research

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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