Published March 12, 2010 | Version v1
Journal article

Antisense repression of sucrose phosphate synthase in transgenic muskmelon alters plant growth and fruit development

  • 1. College of Horticulture Science and Engineering, State Key Laboratory of Crop Biology, Shandong Agricultural University, Tai'an, Shandong 271018 (China)

Description

To unravel the roles of sucrose phosphate synthase (SPS) in muskmelon (Cucumis melo L.), we reduced its activity in transgenic muskmelon plants by an antisense approach. For this purpose, an 830 bp cDNA fragment of muskmelon sucrose phosphate synthase was expressed in antisense orientation behind the 35S promoter of the cauliflower mosaic virus. The phenotype of the antisense plants clearly differed from that of control plants. The transgenic plant leaves were markedly smaller, and the plant height and stem diameter were obviously shorter and thinner. Transmission electron microscope observation revealed that the membrane degradation of chloroplast happened in transgenic leaves and the numbers of grana and grana lamella in the chloroplast were significantly less, suggesting that the slow growth and weaker phenotype of transgenic plants may be due to the damage of the chloroplast ultrastructure, which in turn results in the decrease of the net photosynthetic rate. The sucrose concentration and levels of sucrose phosphate synthase decreased in transgenic mature fruit, and the fruit size was smaller than the control fruit. Together, our results suggest that sucrose phosphate synthase may play an important role in regulating the muskmelon plant growth and fruit development.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2010.01.124

Additional details

Identifiers

DOI
10.1016/j.bbrc.2010.01.124;
PII
S0006-291X(10)00189-0;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
393
Journal Issue
3
Journal Page Range
p. 365-370
ISSN
0006-291X
CODEN
BBRCA9

Optional Information

Copyright
Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.