• Authors: Schwich OD. et al.
  • Year: 2021
  • Journal: Genome Biol . 22(1)
  • Applications: in vitro / DNA, esiRNA / jetOPTIMUS, jetPRIME
  • Cell type: P19
    Description: Mouse embryonic teratocarcinoma cells


For the reporter gene assays 5 μg of each plasmid were transfected per 10 cm cell culture dish for 24 h using JetOPTIMUS according to the manufacturer’s instructions. Cells were starved with Opti-MEM® for 4 h prior to transfection. Per 10 cm cell culture dish, 5 μg purified esiRNAs were transfected for 36 h (SRSF3 & SRSF7) and 48 h (CPSF6) using JetPRIME according to the manufacturer’s instructions. EsiRNAs against GFP (SRSF3 and SRSF7) or Luciferase (CPSF6) were used as controls.


Background: Alternative polyadenylation (APA) refers to the regulated selection of polyadenylation sites (PASs) in transcripts, which determines the length of their 3' untranslated regions (3'UTRs). We have recently shown that SRSF3 and SRSF7, two closely related SR proteins, connect APA with mRNA export. The mechanism underlying APA regulation by SRSF3 and SRSF7 remained unknown. Results: Here we combine iCLIP and 3'-end sequencing and find that SRSF3 and SRSF7 bind upstream of proximal PASs (pPASs), but they exert opposite effects on 3'UTR length. SRSF7 enhances pPAS usage in a concentration-dependent but splicing-independent manner by recruiting the cleavage factor FIP1, generating short 3'UTRs. Protein domains unique to SRSF7, which are absent from SRSF3, contribute to FIP1 recruitment. In contrast, SRSF3 promotes distal PAS (dPAS) usage and hence long 3'UTRs directly by counteracting SRSF7, but also indirectly by maintaining high levels of cleavage factor Im (CFIm) via alternative splicing. Upon SRSF3 depletion, CFIm levels decrease and 3'UTRs are shortened. The indirect SRSF3 targets are particularly sensitive to low CFIm levels, because here CFIm serves a dual function; it enhances dPAS and inhibits pPAS usage by binding immediately downstream and assembling unproductive cleavage complexes, which together promotes long 3'UTRs. Conclusions: We demonstrate that SRSF3 and SRSF7 are direct modulators of pPAS usage and show how small differences in the domain architecture of SR proteins can confer opposite effects on pPAS regulation.