RNA Specificity and Autoregulation of DDX17, a Modulator of MicroRNA Biogenesis.

Cell Rep

Cecil H. and Ida Green Center for Reproductive Biology Sciences and Division of Basic Reproductive Biology Research, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Department of Biophysics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Electronic address:

Published: December 2019

AI Article Synopsis

  • DDX17 is a multifunctional helicase that plays a crucial role in RNA processes, particularly in the maturation of microRNAs.
  • Through structural analysis, researchers found that DDX17's core catalytic domains can recognize specific RNA sequences, helping to remodel primary microRNAs and enhance their processing by Drosha.
  • An intramolecular interaction within DDX17 self-regulates its ATPase activity, linking RNA recognition to its functional outcomes.

Article Abstract

DDX17, a DEAD-box ATPase, is a multifunctional helicase important for various RNA functions, including microRNA maturation. Key questions for DDX17 include how it recognizes target RNAs and influences their structures, as well as how its ATPase activity may be regulated. Through crystal structures and biochemical assays, we show the ability of the core catalytic domains of DDX17 to recognize specific sequences in target RNAs. The RNA sequence preference of the catalytic core is critical for DDX17 to directly bind and remodel a specific region of primary microRNAs 3' to the mature sequence, and consequently enhance processing by Drosha. Furthermore, we identify an intramolecular interaction between the N-terminal tail and the DEAD domain of DDX17 to have an autoregulatory role in controlling the ATPase activity. Thus, we provide the molecular basis for how cognate RNA recognition and functional outcomes are linked for DDX17.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953907PMC
http://dx.doi.org/10.1016/j.celrep.2019.11.059DOI Listing

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