4.7 Article

AUF1 promotes let-7b loading on Argonaute 2

Journal

GENES & DEVELOPMENT
Volume 29, Issue 15, Pages 1599-1604

Publisher

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.263749.115

Keywords

Argonaute; RISC; hnRNP D; microRNA; ribonucleoprotein complex

Funding

  1. National Institute on Aging-Intramural Research Program (National Institutes of Health)
  2. American Heart Association grant [11PRE6900008]
  3. National Institutes of Health grant [R01 CA102428]
  4. National Institute of Arthritis and Musculoskeletal and Skin Diseases-Intramural Research Program (National Institutes of Health)
  5. Charles H. Revson Foundation
  6. Howard Hughes Medical Institute
  7. Starr Cancer Foundation
  8. Creative Research Initiatives (Physical Genetics Laboratory) of the National Research Foundation of Korea [2009-0081562]
  9. Korean Ministry of Science, ICT, and Future Planning [NRF-M1AXA002-2011-0031416, 2011-0031955, N1014002]
  10. NATIONAL CANCER INSTITUTE [R01CA102428] Funding Source: NIH RePORTER
  11. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [ZIAAR041200] Funding Source: NIH RePORTER
  12. NATIONAL INSTITUTE ON AGING [ZICAG000616, ZIAAG000393] Funding Source: NIH RePORTER

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Eukaryotic gene expression is tightly regulated post-transcriptionally by RNA-binding proteins (RBPs) and microRNAs. The RBP AU-rich-binding factor 1 (AUF1) isoform p37 was found to have high affinity for the microRNA let-7b in vitro (K-d = similar to 6 nM) in cells. Ribonucleoprotein immunoprecipitation, in vitro association, and single-molecule-binding analyses revealed that AUF1 promoted let-7b loading onto Argonaute 2 (AGO2), the catalytic component of the RNA-induced silencing complex (RISC). In turn, AGO2-let-7 triggered target mRNA decay. Our findings uncover a novel mechanism by which AUF1 binding and transfer of microRNA let-7 to AGO2 facilitates let-7-elicited gene silencing.

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