TY - JOUR
T1 - The helicase and RNaseIIIa domains of Arabidopsis Dicer-Like1 modulate catalytic parameters during MicroRNA biogenesis
AU - Liu, Chenggang
AU - Axtell, Michael J.
AU - Fedoroff, Nina V.
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: This work was supported by the U.S. National Science Foundation (grant nos. 0718051 to M.J.A. and 0640186 to N.V.F.).
PY - 2012/4/3
Y1 - 2012/4/3
N2 - Dicer-Like1 (DCL1), an RNaseIII endonuclease, and Hyponastic Leaves1 (HYL1), a double-stranded RNA-binding protein, are core components of the plant microRNA (miRNA) biogenesis machinery. hyl1 mutants accumulate low levels of miRNAs and display pleiotropic developmental phenotypes. We report the identification of five new hyl1 suppressor mutants, all of which are alleles of DCL1. These new alleles affect either the helicase or the RNaseIIIa domains of DCL1, highlighting the critical functions of these domains. Biochemical analysis of the DCL1 suppressor variants reveals that they process the primary transcript (pri-miRNA) more efficiently than wild-type DCL1, with both higher Kcat and lower Km values. The DCL1 variants largely rescue wild-type miRNA accumulation levels in vivo, but do not rescue the MIRNA processing precision defects of the hyl1 mutant. In vitro, the helicase domain confers ATP dependence on DCL1-catalyzed MIRNA processing, attenuates DCL1 cleavage activity, and is required for precise MIRNA processing of some substrates. © 2012 American Society of Plant Biologists.
AB - Dicer-Like1 (DCL1), an RNaseIII endonuclease, and Hyponastic Leaves1 (HYL1), a double-stranded RNA-binding protein, are core components of the plant microRNA (miRNA) biogenesis machinery. hyl1 mutants accumulate low levels of miRNAs and display pleiotropic developmental phenotypes. We report the identification of five new hyl1 suppressor mutants, all of which are alleles of DCL1. These new alleles affect either the helicase or the RNaseIIIa domains of DCL1, highlighting the critical functions of these domains. Biochemical analysis of the DCL1 suppressor variants reveals that they process the primary transcript (pri-miRNA) more efficiently than wild-type DCL1, with both higher Kcat and lower Km values. The DCL1 variants largely rescue wild-type miRNA accumulation levels in vivo, but do not rescue the MIRNA processing precision defects of the hyl1 mutant. In vitro, the helicase domain confers ATP dependence on DCL1-catalyzed MIRNA processing, attenuates DCL1 cleavage activity, and is required for precise MIRNA processing of some substrates. © 2012 American Society of Plant Biologists.
UR - http://hdl.handle.net/10754/562151
UR - http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406889
UR - http://www.scopus.com/inward/record.url?scp=84861875067&partnerID=8YFLogxK
U2 - 10.1104/pp.112.193508
DO - 10.1104/pp.112.193508
M3 - Article
C2 - 22474216
SN - 0032-0889
VL - 159
SP - 748
EP - 758
JO - PLANT PHYSIOLOGY
JF - PLANT PHYSIOLOGY
IS - 2
ER -