Suppr超能文献

缺乏胞质谷氨酰胺合成酶1;2活性会降低水稻幼苗腋芽生长所需细胞分裂素的氮依赖性生物合成。

Lack of Cytosolic Glutamine Synthetase1;2 Activity Reduces Nitrogen-Dependent Biosynthesis of Cytokinin Required for Axillary Bud Outgrowth in Rice Seedlings.

作者信息

Ohashi Miwa, Ishiyama Keiki, Kojima Soichi, Kojima Mikiko, Sakakibara Hitoshi, Yamaya Tomoyuki, Hayakawa Toshihiko

机构信息

Graduate School of Agricultural Science, Tohoku University, Aoba, Sendai, Japan.

RIKEN Center for Sustainable Resource Science, Tsurumi, Yokohama, Japan.

出版信息

Plant Cell Physiol. 2017 Apr 1;58(4):679-690. doi: 10.1093/pcp/pcx022.

Abstract

A mutation abolishing cytosolic glutamine synthetase1;2 (GS1;2) activity impairs assimilation of ammonium into glutamine in both roots and basal portions of shoots, and severely decreases axillary bud outgrowth (tillering) in mutant rice seedlings. Although the gs1;2 mutant phenotype is independent of strigolactone, which inhibits tillering, it also demonstrates glutamine- or related metabolite-responsive biosynthesis of cytokinin (CK), which promotes tillering. Here, we examined the connection between GS1;2 and CK biosynthesis during tillering, focusing on basal portions of the shoots as well as apical and axillary bud meristems in the gs1;2 mutant. Despite a sufficient ammonium supply, decreases in precursor CK contents and a decrease in ammonium assimilation into glutamine were observed in basal portions of mutant shoots. Reintroducing expression of OsGS1;2 cDNA driven by its own promoter restored precursor CK contents and ammonium assimilation to wild-type levels. In basal portions of the shoots, glutamine-responsive adenosine phosphate-isopentenyltransferase4 (OsIPT4), which is also predominant in rice roots, was the predominant isogene for IPT, which synthesizes CK. Cell-specific expression of OsIPT4 in phloem companion cells in nodal vascular anastomoses connected to the axillary bud vasculature also decreased in the gs1;2 mutant. Expression of CK-responsive type-A response regulator genes as local indicators of active CKs was also abolished in the axillary bud meristem of the mutant. These results suggest that the lack of GS1;2 activity decreased levels of glutamine or a related metabolite required for CK biosynthesis, causing a deficiency in active CK in the axillary bud meristem necessary for tillering.

摘要

一种消除胞质谷氨酰胺合成酶1;2(GS1;2)活性的突变会损害水稻根和地上部基部将铵同化为谷氨酰胺的过程,并严重降低突变体水稻幼苗的腋芽生长(分蘖)。尽管gs1;2突变体表型独立于抑制分蘖的独脚金内酯,但它也表明了促进分蘖的细胞分裂素(CK)的谷氨酰胺或相关代谢物响应性生物合成。在这里,我们研究了分蘖过程中GS1;2与CK生物合成之间的联系,重点关注gs1;2突变体地上部基部以及顶端和腋芽分生组织。尽管铵供应充足,但在突变体地上部基部观察到前体CK含量下降以及铵同化为谷氨酰胺的过程减少。由其自身启动子驱动的OsGS1;2 cDNA的重新表达将前体CK含量和铵同化恢复到野生型水平。在地上部基部,在水稻根中也占主导地位的谷氨酰胺响应性磷酸腺苷 - 异戊烯基转移酶4(OsIPT4)是合成CK的IPT的主要同基因。与腋芽维管束相连的节间维管束中韧皮部伴细胞中OsIPT4的细胞特异性表达在gs1;2突变体中也降低。作为活性CK局部指标的CK响应型A响应调节基因的表达在突变体的腋芽分生组织中也被消除。这些结果表明,GS1;2活性的缺乏降低了CK生物合成所需的谷氨酰胺或相关代谢物的水平,导致分蘖所需的腋芽分生组织中活性CK缺乏。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验