RT Journal Article SR Electronic T1 SID-1 domains important for dsRNA import in C. elegans JF bioRxiv FD Cold Spring Harbor Laboratory SP 156703 DO 10.1101/156703 A1 Jennifer S. Whangbo A1 Alexandra S. Weisman A1 Jiajie Lu A1 Jeiwook Chae A1 Craig P. Hunter YR 2017 UL http://biorxiv.org/content/early/2017/06/27/156703.abstract AB In the nematode Caenorhabditis elegans, RNA interference (RNAi) triggered by double-stranded RNA (dsRNA) spreads systemically to cause gene silencing throughout the organism and its progeny. We confirm that Caenorhabditis nematode SID-1 orthologs have dsRNA transport activity and demonstrate that the SID-1 paralog CHUP-1 does not transport dsRNA. Sequence comparison of these similar proteins, in conjunction with analysis of loss-of-function missense alleles identifies several conserved 2-7 amino acid microdomains within the extracellular domain that are important for dsRNA transport. Among these missense alleles, we identify and characterize a sid-1 allele, qt95, which causes tissue-specific silencing defects most easily explained as a systemic RNAi export defect. However, we conclude from genetic and biochemical analyses that sid-1(qt95) disrupts only import and speculate that the apparent export defect is caused by the cumulative effect of sequentially impaired dsRNA import steps.Thus, consistent with previous studies, we fail to detect a requirement for sid-1 in dsRNA export, but demonstrate for the first time that SID-1 functions in the intestine to support environmental RNAi.