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GRAS transcription factors regulate cell division planes in moss overriding the default rule.

Masaki IshikawaAyaka FujiwaraKen KosetsuYuta HoriuchiNaoya KamamotoNaoyuki UmakawaYosuke TamadaLiechi ZhangKatsuyoshi MatsushitaGergo PalfalviTomoaki NishiyamaSota KitasakiYuri MasudaYoshiki ShirozaMunenori KitagawaToru NakamuraHongchang CuiYuji HiwatashiYukiko KabeyaShuji ShigenobuTsuyoshi AoyamaKagayaki KatoTakashi MurataKoichi FujimotoPhilip N BenfeyMitsuyasu HasebeRumiko Kofuji
Published in: Proceedings of the National Academy of Sciences of the United States of America (2023)
Plant cells are surrounded by a cell wall and do not migrate, which makes the regulation of cell division orientation crucial for development. Regulatory mechanisms controlling cell division orientation may have contributed to the evolution of body organization in land plants. The GRAS family of transcription factors was transferred horizontally from soil bacteria to an algal common ancestor of land plants. SHORTROOT ( SHR ) and SCARECROW ( SCR ) genes in this family regulate formative periclinal cell divisions in the roots of flowering plants, but their roles in nonflowering plants and their evolution have not been studied in relation to body organization. Here, we show that SHR cell autonomously inhibits formative periclinal cell divisions indispensable for leaf vein formation in the moss Physcomitrium patens , and SHR expression is positively and negatively regulated by SCR and the GRAS member LATERAL SUPPRESSOR , respectively. While precursor cells of a leaf vein lacking SHR usually follow the geometry rule of dividing along the division plane with the minimum surface area, SHR overrides this rule and forces cells to divide nonpericlinally. Together, these results imply that these bacterially derived GRAS transcription factors were involved in the establishment of the genetic regulatory networks modulating cell division orientation in the common ancestor of land plants and were later adapted to function in flowering plant and moss lineages for their specific body organizations.
Keyphrases
  • single cell
  • transcription factor
  • cell therapy
  • poor prognosis
  • gene expression
  • cell wall
  • cell cycle arrest
  • genome wide
  • long non coding rna
  • cell proliferation
  • cell death
  • copy number
  • binding protein
  • solid state