Ishiwatari Y, Fujiwara T, McFarland K C, Nemoto K, Hayashi H, Chino M, Lucas W J
Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, University of Tokyo, Japan.
Planta. 1998 May;205(1):12-22. doi: 10.1007/s004250050291.
Rice (Oryza sativa L.) phloem sieve tubes contain RPP13-1, a thioredoxin h protein that moves around the plant via the translocation stream. Such phloem-mobile proteins are thought to be synthesized in the companion cells prior to being transferred, through plasmodesmata, to the enucleate sieve-tube members. In this study, in-situ hybridization experiments confirmed that expression of RPP13-1 is restricted to companion cells within the mature phloem. To test the hypothesis that RPP13-1 enters the sieve tube, via plasmodesmata, recombinant RPP13-1 was expressed in Escherichia coli, extracted, purified and fluorescently labeled with fluorescein isothiocyanate (FITC) for use in microinjection experiments into tobacco (Nicotiana tabacum L.) mesophyll cells. The FITC-RPP13-1 moved from the injected cell into surrounding cells, whereas the E. coli thioredoxin, an evolutionary homolog of RPP13-1, when similarly labeled and injected, failed to move in this same experimental system. In addition, co-injection of RPP13-1 and FITC-dextrans established that RPP13-1 can induce an increase in plasmodesmal size exclusion limit to a value greater than 9.4 but less than 20 kDa. Nine mutant forms of RPP13-1 were constructed and tested for their capacity to move from cell to cell; two such mutants were found to be incapable of movement. Crystal-structure prediction studies were performed on wild-type and mutant RPP13-1 to identify the location of structural motifs required for protein trafficking through plasmodesmata. These studies are discussed with respect to plasmodesmal-mediated transport of macromolecules within the companion cell-sieve tube complex.
水稻(Oryza sativa L.)韧皮部筛管含有RPP13-1,一种硫氧还蛋白h,它通过转运流在植物体内移动。这类韧皮部可移动蛋白被认为是在伴胞中合成,然后通过胞间连丝转移到无核的筛管分子中。在本研究中,原位杂交实验证实RPP13-1的表达仅限于成熟韧皮部的伴胞。为了验证RPP13-1通过胞间连丝进入筛管的假说,重组RPP13-1在大肠杆菌中表达、提取、纯化,并用异硫氰酸荧光素(FITC)进行荧光标记,用于烟草(Nicotiana tabacum L.)叶肉细胞的显微注射实验。FITC-RPP13-1从注射的细胞移动到周围细胞,而大肠杆菌硫氧还蛋白,RPP13-1的进化同源物,在进行类似标记和注射时,在同一实验系统中未能移动。此外,RPP13-1与FITC-葡聚糖共注射表明,RPP13-1可诱导胞间连丝大小排阻极限增加,达到大于9.4 kDa但小于20 kDa的值。构建了九种RPP13-1突变体形式,并测试它们在细胞间移动的能力;发现其中两种突变体无法移动。对野生型和突变型RPP13-1进行了晶体结构预测研究,以确定蛋白质通过胞间连丝运输所需结构基序的位置。结合伴胞-筛管复合体中胞间连丝介导的大分子运输对这些研究进行了讨论。