Futagami Kazutaka, Tsuzuki Masayuki, Yoshida Mika, Watanabe Yuichiro
Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Tokyo 153-8902, Japan.
Faculty of Agriculture and Marine Sciences, Graduate School of Integrated Arts and Sciences, Kochi University, Nankoku, Kochi 783-8502, Japan.
J Exp Bot. 2025 Aug 21;76(12):3378-3389. doi: 10.1093/jxb/eraf148.
miRNAs were initially detected as ~20-22 nt sequences in plants. For decades miRNA-mediated regulation of target gene expression has been characterized in many cases. The sequences of miR159/319 family miRNAs are conserved among land plants. The roles of miR159/319 have been comprehensively characterized in development of dicot and monocot plants. However, their biological function in bryophytes remains enigmatic. A model bryophyte Marchantia polymorpha also encodes miR319 at two loci and expresses the miRNA. We used a CRISPR/Cas9 system to edit genome sequences at MpMIR319a and/or MpMIR319b loci. The mutant lines developed relatively few gemma cups and gemmae, suggesting that MpmiR319 targets MpRKD or MpR2R3-MYB21 transcripts and suppresses their expression. We constructed miR319-resistant MpRKD (mMpRKD) and MpR2R3-MYB21 (mMpR2R3-MYB21) by decreasing the complementarity to miR319. Introduction of mMpRKD resulted in gemma/gemma cup-less liverwort mutants, but mMpR2R3-MYB21 did not. Transcription fusion constructs between the MpRKD promoter and β-glucuronidase showed that the gene is expressed in the rim and bottom of gemma cups. We found that the mir319a/mir319b double mutant could form gemma cups but of different sizes in a unpredictable arrangement when planted on vermiculite. These results together suggest that miR319 guides the formation of gemma cups/gemmae in standard positions in collaboration with MpRKD.
miRNA最初是在植物中被检测为约20 - 22个核苷酸的序列。几十年来,miRNA介导的靶基因表达调控在许多情况下已得到表征。miR159/319家族miRNA的序列在陆地植物中是保守的。miR159/319在双子叶植物和单子叶植物发育中的作用已得到全面表征。然而,它们在苔藓植物中的生物学功能仍然是个谜。模式苔藓植物地钱也在两个位点编码miR319并表达该miRNA。我们使用CRISPR/Cas9系统编辑MpMIR319a和/或MpMIR319b位点的基因组序列。突变株产生的芽杯和芽孢相对较少,这表明MpmiR319靶向MpRKD或MpR2R3 - MYB21转录本并抑制它们的表达。我们通过降低与miR319的互补性构建了抗miR319的MpRKD(mMpRKD)和MpR2R3 - MYB21(mMpR2R3 - MYB21)。导入mMpRKD导致产生无芽孢/芽杯的地钱突变体,但导入mMpR2R3 - MYB21则不会。MpRKD启动子与β - 葡萄糖醛酸酶之间的转录融合构建体表明该基因在芽杯的边缘和底部表达。我们发现,当种植在蛭石上时,mir319a/mir319b双突变体可以形成芽杯,但大小不同且排列不可预测。这些结果共同表明,miR319与MpRKD协同引导芽杯/芽孢在标准位置的形成。