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CBL-相互作用蛋白激酶 25 有助于根分生组织的发育。

CBL-interacting protein kinase 25 contributes to root meristem development.

机构信息

National Institute of Plant Genome Research, Aruna Asaf Ali Marg, New Delhi, India.

出版信息

J Exp Bot. 2019 Jan 1;70(1):133-147. doi: 10.1093/jxb/ery334.

Abstract

Co-ordination of auxin and cytokinin activities determines root meristem size during post-embryonic development. Calcineurin B-like proteins (CBLs) and their interacting protein kinases (CIPKs) constitute signaling modules that relay calcium signals. Here we report that CIPK25 is involved in regulating the root meristem size. Arabidopsis plants lacking CIPK25 expression displayed a short root phenotype and a slower root growth rate with fewer meristem cells. This phenotype was rescued by restoration of CIPK25 expression. CIPK25 interacted with CBL4 and -5, and displayed strong gene expression in the flower and root, except in the cell proliferation domain in the root apical meristem. Its expression in the root was positively and negatively regulated by auxin and cytokinin, respectively. The cipk25 T-DNA insertion line was compromised in auxin transport and auxin-responsive promoter activity. The cipk25 mutant line showed altered expression of auxin efflux carriers (PIN1 and PIN2) and an Aux/IAA family gene SHY2. Decreased PIN1 and PIN2 expression in the cipk25 mutant line was completely restored when combined with a SHY2 loss-of-function mutation, resulting in recovery of root growth. SHY2 and PIN1 expression was partially regulated by cytokinin even in the absence of CIPK25, suggesting a CIPK25-independent cytokinin signaling pathway(s). Our results revealed that CIPK25 plays an important role in the co-ordination of auxin and cytokinin signaling in root meristem development.

摘要

生长素和细胞分裂素活性的协调决定了胚胎后期发育过程中的根分生组织大小。钙调神经磷酸酶 B 样蛋白 (CBL) 和其相互作用的蛋白激酶 (CIPK) 构成了传递钙信号的信号模块。本文报道 CIPK25 参与调控根分生组织大小。缺乏 CIPK25 表达的拟南芥植株表现出短根表型和较慢的根生长速率,分生组织细胞较少。通过恢复 CIPK25 的表达可以挽救这种表型。CIPK25 与 CBL4 和 -5 相互作用,并在花和根中显示出强烈的基因表达,除了在根顶端分生组织的细胞增殖域。其在根中的表达分别受到生长素和细胞分裂素的正向和负向调节。cipk25 T-DNA 插入系在生长素运输和生长素响应启动子活性方面受到损害。cipk25 突变系表现出生长素外排载体 (PIN1 和 PIN2) 和Aux/IAA 家族基因 SHY2 的表达改变。当与 SHY2 功能丧失突变体结合时,cipk25 突变系中 PIN1 和 PIN2 的表达减少完全恢复,导致根生长恢复。即使在没有 CIPK25 的情况下,SHY2 和 PIN1 的表达也部分受到细胞分裂素的调节,这表明存在 CIPK25 独立的细胞分裂素信号通路。我们的结果表明,CIPK25 在根分生组织发育中生长素和细胞分裂素信号的协调中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e30e/6305191/c316a49f8a41/ery33401.jpg

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