Department of Plant Biology, University of Minesota, St. Paul, Minesota 55108, USA.
Plant Cell. 2010 Dec;22(12):3963-79. doi: 10.1105/tpc.110.080010. Epub 2010 Dec 30.
SODIUM POTASSIUM ROOT DEFECTIVE1 (NaKR1; previously called NPCC6) encodes a soluble metal binding protein that is specifically expressed in companion cells of the phloem. The nakr1-1 mutant phenotype includes high Na(+), K(+), Rb(+), and starch accumulation in leaves, short roots, late flowering, and decreased long-distance transport of sucrose. Using traditional and DNA microarray-based deletion mapping, a 7-bp deletion was found in an exon of NaKR1 that introduced a premature stop codon. The mutant phenotypes were complemented by transformation with the native gene or NaKR1-GFP (green fluorescent protein) and NaKR1-β-glucuronidase fusions driven by the native promoter. NAKR1-GFP was mobile in the phloem; it moved from companion cells into sieve elements and into a previously undiscovered symplasmic domain in the root meristem. Grafting experiments revealed that the high Na(+) accumulation was due mainly to loss of NaKR1 function in the leaves. This supports a role for the phloem in recirculating Na(+) to the roots to limit Na(+) accumulation in leaves. The onset of root phenotypes coincided with NaKR1 expression after germination. The nakr1-1 short root phenotype was due primarily to a decreased cell division rate in the root meristem, indicating a role in root meristem maintenance for NaKR1 expression in the phloem.
SODIUM POTASSIUM ROOT DEFECTIVE1(NaKR1;以前称为 NPCC6)编码一种可溶性金属结合蛋白,该蛋白特异性地在韧皮部的伴胞中表达。nakr1-1 突变体表型包括叶片中高浓度的 Na(+)、K(+)、Rb(+)和淀粉积累、短根、开花晚以及蔗糖的长距离运输减少。使用传统和基于 DNA 微阵列的缺失作图法,在 NaKR1 的一个外显子中发现了一个 7 个碱基对的缺失,导致提前出现了终止密码子。用野生型基因或 NaKR1-GFP(绿色荧光蛋白)和由天然启动子驱动的 NaKR1-β-葡糖苷酸酶融合转化,可互补突变表型。NAKR1-GFP 在韧皮部中是可移动的;它从伴胞转移到筛管,然后进入根分生组织中一个以前未发现的胞质域。嫁接实验表明,高 Na(+)积累主要是由于叶片中 NaKR1 功能丧失所致。这支持了韧皮部在将 Na(+)再循环到根部以限制叶片中 Na(+)积累中的作用。根表型的出现与萌发后 NaKR1 的表达一致。nakr1-1 短根表型主要是由于根分生组织中的细胞分裂率降低,表明 NaKR1 在韧皮部中的表达在根分生组织的维持中起作用。