Determination of in vivo target search kinetics of regulatory noncoding RNA

Author:

Fei Jingyi1,Singh Digvijay2,Zhang Qiucen1,Park Seongjin1,Balasubramanian Divya3,Golding Ido14,Vanderpool Carin K.3,Ha Taekjip1256

Affiliation:

1. Center for the Physics of Living Cells, Department of Physics, University of Illinois, Urbana, IL, USA.

2. Center for Biophysics and Computational Biology, University of Illinois, Urbana, IL, USA.

3. Department of Microbiology, University of Illinois, Urbana, IL, USA.

4. Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX, USA.

5. Carl R. Woese Institute for Genomic Biology, Howard Hughes Medical Institute, Urbana, IL, USA.

6. Howard Hughes Medical Institute, Urbana, IL, USA.

Abstract

RNA kinetics may define regulatory hierarchy The double-helical structure of DNA suggests immediately how nucleic acid polymers can recognize and bind to homologous sequences. Target recognition by RNA is vital in many biological processes. Fei et al. used super-resolution microscopy of tagged RNAs and computer modeling to understand how RNA-RNA base-pairing reactions occur in vivo. They studied a small RNA (sRNA) that targets a messenger RNA (mRNA) for degradation in bacteria. They observed a slow rate of association as the sRNA searched for its mRNA target, but thereafter a fast rate of dissociation. This explains the need for high concentrations of sRNA to cause mRNA degradation. The sRNA found different target mRNAs at different rates, allowing the generation of a regulatory hierarchy. Science , this issue p. 1371

Funder

National Science Foundation

National Institutes of Health

Welch Foundation

Jane Coffin Childs Memorial Fund for Medical Research

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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