Expanding the MicroRNA Targeting Code: Functional Sites with Centered Pairing
Name
Bartel_Expanding the.pdf
Size
1.45 MB
Format
Adobe PDF
Checksum (MD5)
42d2d68d0b7bbc387ba54973104d4c06
Author(s) • • • • •
Shin, Chanseok
Nam, Jin-Wu
Farh, Kyle Kai-How
Chiang, H. Rosaria
Shkumatava, Alena
Bartel, David
Date Issued
June 2010
Journal
Molecular Cell
Publisher
Elsevier
Citation
Shin, Chanseok et al. “Expanding the MicroRNA Targeting Code: Functional Sites with Centered Pairing.” Molecular Cell 38.6 (2010): 789–802.
Version
Author's final manuscript
Abstract
Most metazoan microRNA (miRNA) target sites have perfect pairing to the seed region, located near the miRNA 5′ end. Although pairing to the 3′ region sometimes supplements seed matches or compensates for mismatches, pairing to the central region has been known to function only at rare sites that impart Argonaute-catalyzed mRNA cleavage. Here, we present “centered sites,” a class of miRNA target sites that lack both perfect seed pairing and 3′-compensatory pairing and instead have 11–12 contiguous Watson-Crick pairs to the center of the miRNA. Although centered sites can impart mRNA cleavage in vitro (in elevated Mg[superscript 2+]), in cells they repress protein output without consequential Argonaute-catalyzed cleavage. Our study also identified extensively paired sites that are cleavage substrates in cultured cells and human brain. This expanded repertoire of cleavage targets and the identification of the centered site type help explain why central regions of many miRNAs are evolutionarily conserved.
MIT Department
Harvard University--MIT Division of Health Sciences and Technology
Massachusetts Institute of Technology. Department of Biology
Terms of Use
Creative Commons Attribution-Noncommercial-Share Alike 3.0
Persistent DSpace Link
DOI of Published Version
https://doi.org/10.1016/j.molcel.2010.06.005