CFI 25 Subunit of Cleavage Factor I is Important for Maintaining the Diversity of 3ʹ UTR Lengths in Arabidopsis thaliana (L.) Heynh.

Author:

Zhang Xiaojuan1,Nomoto Mika2ORCID,Garcia-León Marta3,Takahashi Naoki4,Kato Mariko1ORCID,Yura Kei567ORCID,Umeda Masaaki4ORCID,Rubio Vicente3ORCID,Tada Yasuomi2ORCID,Furumoto Tsuyoshi8,Aoyama Takashi1,Tsuge Tomohiko1ORCID

Affiliation:

1. Institute for Chemical Research, Kyoto University, Uji, Kyoto, 611-0011 Japan

2. Center for Gene Research, Nagoya University, Nagoya, Aichi, 464-8601 Japan

3. Plant Molecular Genetics Department, Centro Nacional de Biotecnología-CSIC, Cantoblanco, Madrid 28049, Spain

4. Graduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma, Nara, 630-0192 Japan

5. School of Advanced Science and Engineering, Waseda University, Shinjuku, Tokyo, 162-0041 Japan

6. Graduate School of Humanities and Sciences, Ochanomizu University, Bunkyo, Tokyo, 112-8610 Japan

7. Center for Interdisciplinary AI and Data Science, Ochanomizu University, Bunkyo, Tokyo, 112-8610 Japan

8. Department of Plant Life Science, Graduate School of Agriculture, Ryukoku University, Otsu, Shiga, 520-2194 Japan

Abstract

Abstract Cleavage and polyadenylation at the 3ʹ end of the pre-mRNA is essential for mRNA function, by regulating its translatability, stability and translocation to the cytoplasm. Cleavage factor I (CFI) is a multi-subunit component of the pre-mRNA 3ʹ end processing machinery in eukaryotes. Here, we report that plant CFI 25 subunit of CFI plays an important role in maintaining the diversity of the 3ʹ ends of mRNA. The genome of Arabidopsis thaliana (L.) Heynh. contained four genes encoding three putative CFI subunits (AtCFI 25, AtCFI 59 and AtCFI 68), orthologous to the mammalian CFI subunits. There were two CFI 25 paralogs (AtCFI 25a and AtCFI 25b) that shared homology with human CFI 25. Two null alleles of AtCFI 25a displayed smaller rosette leaves, longer stigmatic papilla, smaller anther, earlier flowering and lower fertility compared to wild-type plants. Null alleles of AtCFI 25b, as well as, plants ectopically expressing full-length cDNA of AtCFI 25a, displayed no obvious morphological defects. AtCFI 25a was shown to interact with AtCFI 25b, AtCFI 68 and itself, suggesting various forms of CFI in plants. Furthermore, we show that AtCFI 25a function was essential for maintaining proper diversity of the 3ʹ end lengths of transcripts coding for CFI subunits, suggesting a self-regulation of the CFI machinery in plants. AtCFI 25a was also important to maintain 3ʹ ends for other genes to different extent. Collectively, AtCFI 25a, but not AtCFI 25b, seemed to play important roles during Arabidopsis development by maintaining proper diversity of the 3ʹ UTR lengths.

Funder

Kyoto University, Research Unit for Development of Global Sustainability

University of Tsukuba, Gene Research Center, Plant Transgenic Design Initiative

Executive Program of Cooperation in the Fields of Science &Technology between the Government of Italy and the Government of Japan

Japan Society for the Promotion of Science

Kyoto University, Collaborative Research Program of Institute for Chemical Research

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science,Physiology,General Medicine

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