Catalytic residues of microRNA Argonautes play a modest role in microRNA star strand destabilization in C. elegans

Author:

Kotagama Kasuen1,Grimme Acadia L12,Braviner Leah3,Yang Bing1,Sakhawala Rima M12,Yu Guoyun1,Benner Lars Kristian1,Joshua-Tor Leemor3,McJunkin Katherine1ORCID

Affiliation:

1. Laboratory of Cellular and Developmental Biology, NIDDK Intramural Research Program , 50 South Drive , Bethesda , MD  20892 , USA

2. Johns Hopkins University Department of Biology , 3400 N. Charles Street , Baltimore , MD  21218 , USA

3. Cold Spring Harbor Laboratory , One Bungtown Road , Cold Spring Harbor, NY  11724 , USA

Abstract

Abstract Many microRNA (miRNA)-guided Argonaute proteins can cleave RNA (‘slicing’), even though miRNA-mediated target repression is generally cleavage-independent. Here we use Caenorhabditis elegans to examine the role of catalytic residues of miRNA Argonautes in organismal development. In contrast to previous work, mutations in presumed catalytic residues did not interfere with development when introduced by CRISPR. We find that unwinding and decay of miRNA star strands is weakly defective in the catalytic residue mutants, with the largest effect observed in embryos. Argonaute-Like Gene 2 (ALG-2) is more dependent on catalytic residues for unwinding than ALG-1. The miRNAs that displayed the greatest (albeit minor) dependence on catalytic residues for unwinding tend to form stable duplexes with their star strand, and in some cases, lowering duplex stability alleviates dependence on catalytic residues. While a few miRNA guide strands are reduced in the mutant background, the basis of this is unclear since changes were not dependent on EBAX-1, an effector of Target-Directed miRNA Degradation (TDMD). Overall, this work defines a role for the catalytic residues of miRNA Argonautes in star strand decay; future work should examine whether this role contributes to the selection pressure to conserve catalytic activity of miRNA Argonautes across the metazoan phylogeny.

Funder

NIDDK

Publisher

Oxford University Press (OUP)

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