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The CLAVATA3/ESR Motif of CLAVATA3 Is Functionally Independent from the Nonconserved Flanking Sequences1

机译:CLAVATA3的CLAVATA3 / ESR主题在功能上与非保守侧翼序列无关

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摘要

It is believed that CLAVATA3 (CLV3) encodes a peptide ligand that interacts with the CLV1/CLV2 receptor complex to limit the number of stem cells in the shoot apical meristem of Arabidopsis thaliana; however, the exact composition of the functional CLV3 product remains a mystery. A recent study on CLV3 shows that the CLV3/ESR (CLE) motif, together with the adjacent C-terminal sequence, is sufficient to execute CLV3 function when fused behind an N-terminal sequence of ERECTA. Here we show that most of the sequences flanking the CLE motif of CLV3 can be deleted without affecting CLV3 function. Using a liquid culture assay, we demonstrate that CLV3p, a synthetic peptide corresponding to the CLE motif of CLV3, is able to restrict the size of the shoot apical meristem in clv3 seedlings but not in clv1 seedlings. In accordance with this decrease in meristem size, application of CLV3p to in vitro-grown clv3 seedlings restricts the expression of the stem cell-promoting transcription factor WUSCHEL. Thus, we propose that the CLE motif is the functional region of CLV3 and that this region acts independently of its adjacent sequences.
机译:相信CLAVATA3(CLV3)编码与CLV1 / CLV2受体复合物相互作用的肽配体,以限制拟南芥茎尖分生组织中干细胞的数量。但是,功能性CLV3产品的确切组成仍然是个谜。最近对CLV3的研究表明,当CLV3 / ESR(CLE)基序与相邻的C端序列一起融合在ERECTA的N端序列后面时,足以执行CLV3功能。在这里,我们显示了在不影响CLV3功能的情况下,可以删除位于CLV3 CLE基序侧翼的大多数序列。使用液体培养测定法,我们证明CLV3p(一种对应于CLV3的CLE基序的合成肽)能够限制clv3幼苗中的茎尖分生组织的大小,但不能限制clv1幼苗中的茎尖分生组织的大小。根据分生组织大小的这种减少,将CLV3p应用于体外生长的clv3幼苗会限制干细胞促进转录因子WUSCHEL的表达。因此,我们建议CLE主题是CLV3的功能区域,并且该区域独立于其相邻序列起作用。

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  • 来源
    《Plant Physiology》 |2006年第4期|p.1284-1292|共9页
  • 作者单位

    Plant Research International, Centre for BioSystems Genomics, 6700 AA Wageningen, The Netherlands (M.F., L.v.d.G., W.J.S.);

    Institute of Plant Physiology, Polish Academy of Sciences, 30–239 Krakow, Poland (E.G.);

    Department of Molecular and Cellular Neurobiology, Free University, 1081 HV Amsterdam, The Netherlands (R.v.d.S., K.W.L.);

    and Center for Signal Transduction and Metabolomics, Key Laboratory of Photosynthesis and Environmental Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China (C.-M.L.);

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