Curriculum Vitaes

Fujiwara Makoto

  (藤原 誠)

Profile Information

Affiliation
Associate Professor, Faculty of Science and Technology, Department of Materials and Life Sciences, Sophia University
Degree
Bachelor(The University of Tokyo)
Master(The University of Tokyo)
Ph. D.(The University of Tokyo)

Researcher number
90332345
J-GLOBAL ID
200901000526942076
researchmap Member ID
5000099166

1) Replication and morphology of plastids in Arabidopsis thaliana
2) Idioblast formation in Egeria densa

(Subject of research)
(1) Genetic control of plastid division.
(2) Cytological analysis of green algae.


Research Interests

 4

Awards

 1

Papers

 64
  • 藤原 誠, 伊藤 竜一
    アグリバイオ, 8(14) 63-69, Dec, 2024  InvitedLead authorCorresponding author
  • 伊藤 竜一, 藤原 誠
    化学と生物, 62(12) 570-578, Dec, 2024  Peer-reviewedLast author
  • Alvin Sanjaya, Ryo Nishijima, Yuki Fujii, Makoto Asano, Kotaro Ishii, Yusuke Kazama, Tomoko Abe, Makoto T. Fujiwara
    Frontiers in Plant Science, 15, Sep, 2024  Peer-reviewedLast authorCorresponding author
    Pre-mRNA splicing is a fundamental process in eukaryotic gene expression, and the mechanism of intron definition, involving the recognition of the canonical GU (5’-splice site) and AG (3’-splice site) dinucleotides by splicing factors, has been postulated for most cases of splicing initiation in plants. Splice site mutations have played crucial roles in unraveling the mechanism of pre-mRNA splicing in planta. Typically, splice site mutations abolish splicing events or activate one or more cryptic splice sites surrounding the mutated region. In this report, we investigated the splicing pattern of the EGY1 gene in an Ar-ion-induced egy1-4 allele of Arabidopsis thaliana. egy1-4 has an AG-to-AC mutation in the 3′-end of intron 3, along with 4-bp substitutions and a 5-bp deletion in adjacent exon 4. RT-PCR, cDNA cloning, and amplicon sequencing analyses of EGY1 revealed that while most wild-type EGY1 mRNAs had a single splicing pattern, egy1-4 mRNAs had multiple splicing defects. Almost half of EGY1 transcripts showed ‘intron retention’ at intron 3, while the other half exhibited activation of 3’ cryptic splice sites either upstream or downstream of the original 3’-splice site. Unexpectedly, around 8% of EGY1 transcripts in egy1-4 exhibited activation of cryptic 5′-splice sites positioned upstream of the authentic 5’-splice site of intron 3. Whole genome resequencing of egy1-4 indicated that it has no other known impactful mutations. These results may provide a rare, but real case of activation of cryptic 5’-splice sites by downstream 3’-splice site/exon mutations in planta.
  • Makoto T Fujiwara, Yasushi Yoshioka, Yusuke Kazama, Tomonari Hirano, Yasuo Niwa, Takashi Moriyama, Naoki Sato, Tomoko Abe, Shigeo Yoshida, Ryuuichi D Itoh
    Plant Physiology, Sep, 2024  Peer-reviewedLead authorCorresponding author
  • Sanjaya A., Fujii Y., Asano M., Abe T., Kazama Y., Fujiwara M.
    RIKEN Accelerator Progress Report, 56 190, Jan, 2024  Peer-reviewedLast authorCorresponding author

Books and Other Publications

 4

Presentations

 54
  • 藤原誠
    COEセミナー, Jan, 2011  Invited
  • Makoto Fujiwara, Yusuke Kazama, Tomoko Abe, Ryuuichi Itoh
    International Conference on Arabidopsis Research, Jun, 2010
  • Fujiwara Makoto, Itoh Ryuuichi, Ishikawa Masayuki, Niwa Yasuo, Sato Naoki, Yoshida Shigeo, Abe Tomoko
    Plant and Cell Physiology Supplement, 2008, The Japanese Society of Plant Physiologists
    In vascular plants, non-photosynthetic plastids, such as amyloplasts for starch storage in tubers and root tips and leucoplasts referred to as non-coloured plastids in roots and other non-green tissues, are controlled by distinct mechanisms from those for leaf chloroplasts in terms of the structure and behaviour. To elucidate these issues, we constructed transgenic Arabidopsis plants, in which the N-terminal plastid targeting sequence from the plastid division factor AtFtsZ1-1 or the Rubisco small subunit is fused to the N-terminus of the green fluorescent protein or its variants and expressed stably under the control of the Cauliflower mosaic virus 35S promoter. By epifluorescence microscopy using living tissues of these plants, we found that leucoplasts in seed integuments take highly filamentous forms and also produce stromules at high frequency. Furthermore, leucoplasts at the onset of amyloplast differentiation were found to display amoeboid-like shape and motility, as revealed by time-lapse epifluorescence microscopy.

Research Projects

 17

Social Activities

 1

Media Coverage

 2