A prometastatic splicing program regulated by SNRPA1 interactions with structured RNA elements

Author:

Fish Lisa1234ORCID,Khoroshkin Matvei1234ORCID,Navickas Albertas1234ORCID,Garcia Kristle1234,Culbertson Bruce1234,Hänisch Benjamin1234,Zhang Steven1234,Nguyen Hoang C. B.5ORCID,Soto Larisa M.67ORCID,Dermit Maria8ORCID,Mardakheh Faraz K.8ORCID,Molina Henrik9ORCID,Alarcón Claudio1011ORCID,Najafabadi Hamed S.67ORCID,Goodarzi Hani1234ORCID

Affiliation:

1. Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA.

2. Department of Urology, University of California, San Francisco, San Francisco, CA 94158, USA.

3. Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA 94158, USA.

4. Bakar Computational Health Sciences Institute, University of California, San Francisco, San Francisco, CA 94158, USA.

5. Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.

6. Department of Human Genetics, McGill University, Montreal, QC H3A 0C7, Canada.

7. McGill Genome Centre, Montreal, QC H3A 0G1, Canada.

8. Centre for Cancer Cell and Molecular Biology, Barts Cancer Institute, Queen Mary University of London, London EC1M 6BQ, UK.

9. Proteome Resource Center, The Rockefeller University, New York, NY 10065, USA.

10. Department of Pharmacology, Yale University School of Medicine, New Haven, CT 06520, USA.

11. Yale Cancer Biology Institute, Yale University, West Haven, CT 06516, USA.

Abstract

Characterizing a cancer spliceosome Cells undergo many genomic changes as they progress toward metastatic cancer. One aspect of this change is to RNA expression and splicing isoforms, but how these differences affect tumor progression is not well characterized. Fish et al. developed a computational framework called pyTEISER that identifies structural cis-regulatory elements that control diverse types of RNA regulation. Applying pyTEISER to models of breast cancer metastasis, they discovered an RNA short-stem-loop element that forms a “structural splicing enhancer” that acts in cis to regulate alternative splicing of RNA transcripts. One of these interactions encompasses the RNA-binding protein SNRPA1 and results in alternative exon inclusion that affects metastatic capacity in xenograft models. Thus, RNA element binding may play a role in splicing regulation and is potentially an important component of the cis-splicing code. Science , this issue p. eabc7531

Funder

National Institutes of Health

Howard Hughes Medical Institute

National Cancer Institute

DOD Peer Reviewed Cancer Research Program

Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco

American College of Surgeons

UCSF Helen Diller Family Comprehensive Cancer Center Breast Oncology Program

Medical Research Council

Canadian Institutes of Health Research

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Cited by 36 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3