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天冬酰胺合成酶1而非天冬酰胺合成酶2,负责在铵供应至水稻根部后天冬酰胺的生物合成。

Asparagine synthetase1, but not asparagine synthetase2, is responsible for the biosynthesis of asparagine following the supply of ammonium to rice roots.

作者信息

Ohashi Miwa, Ishiyama Keiki, Kojima Soichi, Konishi Noriyuki, Nakano Kentaro, Kanno Keiichi, Hayakawa Toshihiko, Yamaya Tomoyuki

机构信息

Graduate School of Agricultural Science, Tohoku University, 1-1 Tsutsumidori-Amamiyamachi, Aoba-ku, Sendai, 981-8555 Japan.

Graduate School of Agricultural Science, Tohoku University, 1-1 Tsutsumidori-Amamiyamachi, Aoba-ku, Sendai, 981-8555 Japan Present address: Cambridge Technology Partners Co. Ltd., 1-1-1 Toyosu, Koto-ku, Tokyo 135-8560 Japan.

出版信息

Plant Cell Physiol. 2015 Apr;56(4):769-78. doi: 10.1093/pcp/pcv005. Epub 2015 Jan 28.

DOI:10.1093/pcp/pcv005
PMID:25634963
Abstract

Asparagine is synthesized from glutamine by the reaction of asparagine synthetase (AS) and is the major nitrogen form in both xylem and phloem sap in rice (Oryza sativa L.). There are two genes encoding AS, OsAS1 and OsAS2, in rice, but the functions of individual AS isoenzymes are largely unknown. Cell type- and NH4(+)-inducible expression of OsAS1 as well as analyses of knockout mutants were carried out in this study to characterize AS1. OsAS1 was mainly expressed in the roots, with in situ hybridization showing that the corresponding mRNA was specifically accumulated in the three cell layers of the root surface (epidermis, exodermis and sclerenchyma) in an NH4(+)-dependent manner. Conversely, OsAS2 mRNA was abundant in leaf blades and sheathes of rice. Although OsAS2 mRNA was detectable in the roots, its content decreased when NH4(+) was supplied. Retrotransposon-mediated knockout mutants lacking AS1 showed slight stimulation of shoot length and slight reduction in root length at the seedling stage. On the other hand, the mutation caused an approximately 80-90% reduction in free asparagine content in both roots and xylem sap. These results suggest that AS1 is responsible for the synthesis of asparagine in rice roots following the supply of NH4(+). Characteristics of the NH4(+)-dependent increase and the root surface cell-specific expression of OsAS1 gene are very similar to our previous results on cytosolic glutamine synthetase1;2 and NADH-glutamate synthase1 in rice roots. Thus, AS1 is apparently coupled with the primary assimilation of NH4(+) in rice roots.

摘要

天冬酰胺由天冬酰胺合成酶(AS)的反应从谷氨酰胺合成,是水稻(Oryza sativa L.)木质部和韧皮部汁液中的主要氮形态。水稻中有两个编码AS的基因,即OsAS1和OsAS2,但单个AS同工酶的功能在很大程度上尚不清楚。本研究对OsAS1进行了细胞类型和NH4(+)诱导表达以及敲除突变体分析,以表征AS1。OsAS1主要在根中表达,原位杂交显示相应的mRNA以NH4(+)依赖的方式特异性积累在根表面的三层细胞(表皮、外皮层和厚壁组织)中。相反,OsAS2 mRNA在水稻的叶片和叶鞘中丰富。虽然在根中可检测到OsAS2 mRNA,但在供应NH4(+)时其含量会降低。缺乏AS1的反转录转座子介导的敲除突变体在幼苗期表现出地上部长度略有增加,根部长度略有减少。另一方面,该突变导致根和木质部汁液中的游离天冬酰胺含量降低约80 - 90%。这些结果表明,AS1负责在供应NH4(+)后水稻根中天冬酰胺的合成。OsAS1基因的NH4(+)依赖性增加和根表面细胞特异性表达的特征与我们之前关于水稻根中细胞质谷氨酰胺合成酶1;2和NADH - 谷氨酸合成酶1的结果非常相似。因此,AS1显然与水稻根中NH4(+)的初级同化作用相关。

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