Chloroplast-Like Organelles Were Found in Enucleate Sieve Elements of Transgenic Plants Overexpressing a Proteinase Inhibitor
Author(s) -
Jun Xie,
Xuezhi Ouyang,
Kuaifei Xia,
Yufeng Huang,
Wen-Bi PAN,
Ying-Peng CAI,
Xinping Xu,
Baojian Li,
Zeng-Fu Xu
Publication year - 2007
Publication title -
bioscience biotechnology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1271/bbb.70362
Subject(s) - cauliflower mosaic virus , biology , chloroplast , transgene , genetically modified crops , transformation (genetics) , western blot , microbiology and biotechnology , botany , biochemistry , gene
SaPIN2a, a plant proteinase inhibitor from nightshade (Solanum americanum), was located to the enucleate sieve elements (SEs) of phloem. The expressed SaPIN2a in transgenic lettuce showed inhibition of plant endogenous trypsin- and chymotrypsin-like activities, suggesting that SaPIN2a can regulate proteolysis in plant cells. To further investigate the physiological role of SaPIN2a, we produced transgenic nightshade and lettuce plants overexpressing SaPIN2a from the cauliflower mosaic virus (CaMV) 35S promoter using Agrobacterium-mediated transformation. Overexpression of SaPIN2a in transgenic plants was demonstrated by northern blot and western blot analysis. SaPIN2a-overexpressing transgenic nightshade plants showed significantly lower height than wild-type plants. Transmission electron microscopy analysis showed that chloroplast-like organelles with thylakoids, which are not present in enucleate SEs of wild-type plants, were present in the enucleate SEs of SaPIN2a-overexpressing transgenic plants. This finding is discussed in terms of the possible role played by SaPIN2a in the regulation of proteolysis in SEs.
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