Identification and subcellular localisation of Sl;INT7: A novel tomato (Solanum lycopersicum Mill.) fruit ripening-related and stress-inducible gene
Mourad A.M. Aboul-Soud and Hany A. El-Shemy
Plant Science, Volume 176, Issue 2, February 2009, Pages 241-247
2009
บทคัดย่อ
The key step in ethylene (C2H4) signalling during tomato fruit ripening is initialized via the direct interaction between C2H4 and specialized membrane-bound receptors, including Never-Ripe (NR), which is strongly induced during ripening. In order to identify novel ripening-related C2H4-dependent components, a yeast two-hybrid interaction screen has previously been employed, in which NR cDNA has been used as bait. This screen has identified a clone corresponding to interacting protein 7 (SI;INT7), through its specific and strong interaction with the NR receptor (L. Alexander, Z. Lin, R. Hackett, I. Wilson and D. Grierson, unpublished work). In this work, our objective was to identify the corresponding NR-interacting gene and subsequently characterize its expression response to various stress treatments, as well as unravelling its subcellular location in the cell. By sequencing and plant database interrogation, SI;INT7 was found to be a small gene with an open reading frame (ORF) of ~243 bb encoding a protein composed of 77 aa that shares no sequence homology with any known gene. Notably, northern analyses demonstrated that SI;INT7 gene expression is up-regulated in response to various stress signalling molecules such as salicylic acid (SA), abscissic acid, jasmonic acid, nitric oxide (NO) and salt, implicating SI;INT7 in biotic and abiotic stress signalling transduction responses. To gain more insight into the possible function of SI;INT7, a construct in which SI;INT7 is C-terminally fused to the green fluorescent protein (GFP) was generated. Subsequently, 35S::SI;INT7::GFP-containing constructs were transiently expressed in both tobacco leaves and onion peels via microprojectiles bombardment. Subsequently, confocal laser microscopic examination of bombarded tobacco and onion tissues revealed that the expression of GFP-SI;INT7 was observed predominantly in the plasma membrane, compared to the location throughout the cell observed with the control GFP construct alone. These results are discussed in the light of our present knowledge of C2H4-mediated control over fruit ripening and degree of cross-talk with other stress signalling pathways.