4.8 Article

The SERRATE protein is involved in alternative splicing in Arabidopsis thaliana

Journal

NUCLEIC ACIDS RESEARCH
Volume 42, Issue 2, Pages 1224-1244

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkt894

Keywords

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Funding

  1. Polish National Science Center [UMO-2011/01/M/NZ2/01435, UMO-2012/05/N/NZ2/00880, UMO-2012/04/NZ2/00127]
  2. Polish Ministry of Science and Higher Education [4631/B/PO1/2010/39]
  3. Biotechnology and Biological Sciences Research Council (BBSRC) [European Research Area network (ERA-NET) Plant Genomics (Plant Alternative Splicing and Abiotic Stress)] [BB/G024979/1]
  4. Scottish Government Rural and Environment Science and Analytical Services division (RESAS)
  5. Adam Mickiewicz University, Faculty of Biology, Poznan, Poland
  6. Biotechnology and Biological Sciences Research Council [BB/G024979/1] Funding Source: researchfish
  7. BBSRC [BB/G024979/1] Funding Source: UKRI

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How alternative splicing (AS) is regulated in plants has not yet been elucidated. Previously, we have shown that the nuclear cap-binding protein complex (AtCBC) is involved in AS in Arabidopsis thaliana. Here we show that both subunits of AtCBC (AtCBP20 and AtCBP80) interact with SERRATE (AtSE), a protein involved in the microRNA biogenesis pathway. Moreover, using a high-resolution reverse transcriptase-polymerase chain reaction AS system we have found that AtSE influences AS in a similar way to the cap-binding complex (CBC), preferentially affecting selection of 5' splice site of first introns. The AtSE protein acts in cooperation with AtCBC: many changes observed in the mutant lacking the correct SERRATE activity were common to those observed in the cbp mutants. Interestingly, significant changes in AS of some genes were also observed in other mutants of plant microRNA biogenesis pathway, hyl1-2 and dcl1-7, but a majority of them did not correspond to the changes observed in the se-1 mutant. Thus, the role of SERRATE in AS regulation is distinct from that of HYL1 and DCL1, and is similar to the regulation of AS in which CBC is involved.

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