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Signaling by the EPFL-ERECTA family coordinates female germline specification through the BZR1 family in Arabidopsis

Cai, Hanyang; Huang, Youmei; Liu, Liping; Zhang, Man; Chai, Mengnan; Xi, Xinpeng; Aslam, Mohammad; Wang, Lulu; Ma, Suzhuo; Su, Han; Liu, Kaichuang; Tian, Yaru; Zhu, Wenhui; Qi, Jingang; Dresselhaus, Thomas; Qin, Yuan*
Science Citation Index Expanded
广东省农业科学院; 广西大学; 福建农林大学; 6; y

摘要

In most flowering plants, the female germline is initiated in the subepidermal L2 layer of ovule primordia forming a single megaspore mother cell (MMC). How signaling from the L1 (epidermal) layer could contribute to the gene regulatory network (GRN) restricting MMC formation to a single cell is unclear. We show that EPIDERMAL PATTERNING FACTOR-like (EPFL) peptide ligands are expressed in the L1 layer, together with their ERECTA family (ERf) receptor kinases, to control female germline specification in Arabidopsis thaliana. EPFL-ERf dependent signaling restricts multiple subepidermal cells from acquiring MMC-like cell identity by activating the expression of the major brassinosteroid (BR) receptor kinase BRASSINOSTEROID INSENSITIVE 1 and the BR-responsive transcription factor BRASSINOZOLE RESISTANT 1 (BZR1). Additionally, BZR1 coordinates female germline specification by directly activating the expression of a nucleolar GTP-binding protein, NUCLEOSTEMIN-LIKE 1 (NSN1), which is expressed in early-stage ovules excluding the MMC. Mutants defective in this GRN form multiple MMCs resulting in a strong reduction of seed set. In conclusion, we uncovered a ligand/receptor-like kinase-mediated signaling pathway acting upstream and coordinating BR signaling via NSN1 to restrict MMC differentiation to a single subepidermal cell. @@@ A ligand/receptor-like kinase-mediated signaling pathway coordinates brassinosteroid signaling via the GTP-binding protein NUCLEOSTEMIN-LIKE 1 to restrict megaspore mother cell differentiation to a single subepidermal cell.

关键词

LIGAND-RECEPTOR PAIRS WILD-TYPE INFLORESCENCE ARCHITECTURE OVULE DEVELOPMENT GENE-EXPRESSION CELL FATE KINASE GROWTH ACTIVATION MEIOSIS