Transcription termination and antitermination of bacterial CRISPR arrays

Author:

Stringer Anne M1,Baniulyte Gabriele2ORCID,Lasek-Nesselquist Erica1,Seed Kimberley D34ORCID,Wade Joseph T12ORCID

Affiliation:

1. Wadsworth Center, New York State Department of Health, Albany, United States

2. Department of Biomedical Sciences, School of Public Health, University at Albany, Albany, United States

3. Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, United States

4. Chan Zuckerberg Biohub, San Francisco, United States

Abstract

A hallmark of CRISPR-Cas immunity systems is the CRISPR array, a genomic locus consisting of short, repeated sequences (‘repeats’) interspersed with short, variable sequences (‘spacers’). CRISPR arrays are transcribed and processed into individual CRISPR RNAs that each include a single spacer, and direct Cas proteins to complementary sequences in invading nucleic acid. Most bacterial CRISPR array transcripts are unusually long for untranslated RNA, suggesting the existence of mechanisms to prevent premature transcription termination by Rho, a conserved bacterial transcription termination factor that rapidly terminates untranslated RNA. We show that Rho can prematurely terminate transcription of bacterial CRISPR arrays, and we identify a widespread antitermination mechanism that antagonizes Rho to facilitate complete transcription of CRISPR arrays. Thus, our data highlight the importance of transcription termination and antitermination in the evolution of bacterial CRISPR-Cas systems.

Funder

National Institute of General Medical Sciences

National Institute of Allergy and Infectious Diseases

Burroughs Wellcome Fund

Publisher

eLife Sciences Publications, Ltd

Subject

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

Reference69 articles.

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