Zhang Zai-Bao, Yang Guang, Arana Fernando, Chen Zhen, Li Yan, Xia Hui-Jun
Key Laboratory of MOE for Plant Developmental Biology, College of Life Sciences, Wuhan University, Wuhan, Hubei 430072, China.
Plant Physiol. 2007 Jun;144(2):942-51. doi: 10.1104/pp.106.092163. Epub 2007 Apr 13.
The Arabidopsis (Arabidopsis thaliana) inositol polyphosphate 6-/3-kinase gene (AtIpk2beta) is known to participate in inositol phosphate metabolism. However, little is known about its physiological functions in higher plants. Here, we report that AtIpk2beta regulates Arabidopsis axillary shoot branching. By overexpressing AtIpk2beta in the wild type and mutants, we found that overexpression of AtIpk2beta leads to more axillary shoot branches. Further analysis of AtIpk2beta overexpression lines showed that axillary meristem forms earlier and the bud outgrowth rate is also accelerated, resulting in more axillary shoot branches. The AtIpk2beta promoter/beta-glucuronidase (GUS) fusion (AtIpk2betaGUS) expression pattern is similar to that of the auxin reporter DR5GUS. Moreover, AtIpk2beta can be induced in response to exogenous indole-3-acetic acid (IAA) treatments. In addition, AtIpk2beta overexpression plants exhibit IAA-related phenotypes and are more resistant to exogenous IAA treatments. Further analysis employing reverse transcription-polymerase chain reaction shows that some genes, including auxin-biosynthesis (CYP83B1), auxin-transport (PIN4), and auxin-mediated branching genes (MAX4 and SPS), are regulated by AtIpk2beta. Taken together, our data provide insights into a role for AtIpk2beta in axillary shoot branching through the auxin signaling pathway.
已知拟南芥(Arabidopsis thaliana)肌醇多磷酸6-/3-激酶基因(AtIpk2beta)参与肌醇磷酸代谢。然而,其在高等植物中的生理功能却鲜为人知。在此,我们报道AtIpk2beta调控拟南芥腋芽分枝。通过在野生型和突变体中过表达AtIpk2beta,我们发现AtIpk2beta过表达导致更多的腋芽分枝。对AtIpk2beta过表达株系的进一步分析表明,腋生分生组织形成更早,芽的生长速率也加快,从而产生更多的腋芽分枝。AtIpk2beta启动子/β-葡萄糖醛酸酶(GUS)融合体(AtIpk2betaGUS)的表达模式与生长素报告基因DR5GUS相似。此外,AtIpk2beta可对外源吲哚-3-乙酸(IAA)处理产生响应而被诱导。另外,AtIpk2beta过表达植株表现出与IAA相关的表型,并且对外源IAA处理更具抗性。采用逆转录-聚合酶链反应的进一步分析表明,一些基因,包括生长素生物合成基因(CYP83B1)、生长素运输基因(PIN4)以及生长素介导的分枝基因(MAX4和SPS),受AtIpk2beta调控。综上所述,我们的数据揭示了AtIpk2beta通过生长素信号通路在腋芽分枝中所起的作用。