Genome-wide chromosomal association of Upf1 is linked to Pol II transcription in Schizosaccharomyces pombe

Author:

De Sandip12,Edwards David M3ORCID,Dwivedi Vibha1,Wang Jianming1,Varsally Wazeer1,Dixon Hannah L1,Singh Anand K14,Owuamalam Precious O1,Wright Matthew T1,Summers Reece P1,Hossain Md Nazmul15,Price Emily M1,Wojewodzic Marcin W16ORCID,Falciani Francesco1,Hodges Nikolas J1,Saponaro Marco7ORCID,Tanaka Kayoko8,Azzalin Claus M9,Baumann Peter10,Hebenstreit Daniel3ORCID,Brogna Saverio1ORCID

Affiliation:

1. School of Biosciences and Birmingham Centre of Genome Biology (BCGB), University of Birmingham, UK

2. Division of Cellular and Gene Therapies, Tumor Vaccines and Biotechnology Branch, Center for Biologics and Evaluation Research, US Food and Drug Administration, Silver Spring, MD, USA

3. School of Life Sciences, University of Warwick, Coventry, UK

4. Interdisciplinary School of Life Sciences, Banaras Hindu University, Varanasi 221005, India

5. Department of Microbial Biotechnology, Faculty of Biotechnology and Genetic Engineering, Sylhet Agricultural University, Sylhet 3100, Bangladesh

6. Department of Environmental Health, Norwegian Institute of Public Health, Oslo, Norway & Department of Research, Cancer Registry of Norway, Oslo University Hospital, Oslo, Norway & Environmental Genomics, School of Biosciences, University of Birmingham, Birmingham, UK

7. Institute of Cancer and Genomic Sciences, University of Birmingham, UK

8. Department of Molecular and Cell Biology, University of Leicester, UK

9. Instituto de Medicina Molecular João Lobo Antunes (iMM), Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal

10. Johannes Gutenberg University, Mainz, Germany

Abstract

Abstract Although the RNA helicase Upf1 has hitherto been examined mostly in relation to its cytoplasmic role in nonsense mediated mRNA decay (NMD), here we report high-throughput ChIP data indicating genome-wide association of Upf1 with active genes in Schizosaccharomyces pombe. This association is RNase sensitive, correlates with Pol II transcription and mRNA expression levels. Changes in Pol II occupancy were detected in a Upf1 deficient (upf1Δ) strain, prevalently at genes showing a high Upf1 relative to Pol II association in wild-type. Additionally, an increased Ser2 Pol II signal was detected at all highly transcribed genes examined by ChIP-qPCR. Furthermore, upf1Δ cells are hypersensitive to the transcription elongation inhibitor 6-azauracil. A significant proportion of the genes associated with Upf1 in wild-type conditions are also mis-regulated in upf1Δ. These data envisage that by operating on the nascent transcript, Upf1 might influence Pol II phosphorylation and transcription.

Funder

Wellcome Trust

Royal Society

DBT Ramalingaswami

Biotechnology and Biological Sciences Research Council

Bangabandhu Science and Technology Fellowship Trust

Publisher

Oxford University Press (OUP)

Subject

Genetics

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