Identification of differentially-expressed genes in response to salt stress in the salt-tolerant Sri Lankan rice variety At354

被引:1
作者
Zahra, A. R. F. [1 ]
De Costa, D. M. [1 ]
De Costa, W. A. J. M. [2 ]
机构
[1] Univ Peradeniya, Fac Agr, Dept Agr Biol, Peradeniya, Sri Lanka
[2] Univ Peradeniya, Fac Agr, Dept Crop Sci, Peradeniya, Sri Lanka
来源
JOURNAL OF THE NATIONAL SCIENCE FOUNDATION OF SRI LANKA | 2013年 / 41卷 / 02期
基金
美国国家科学基金会;
关键词
Differential hybridization; gene expression; Oryza sativa; salt stress; salt tolerant genes; ZINC-FINGER PROTEIN; TRANSLATION INITIATION-FACTOR; TRANSFERASE GENE; S-TRANSFERASE; OSDREB GENES; PLANT-GROWTH; SATIVA L; RT-PCR; DROUGHT; ARABIDOPSIS;
D O I
10.4038/jnsfsr.v41i2.5704
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Rice is highly sensitive to salt stress, an expanding abiotic stress factor that limits rice yield improvement. Development of salt tolerant rice varieties based on molecular breeding methods requires identification of genes responsible. for various mechanisms and responses that contribute to salt tolerance. The objective of the present work was to identify genes, which are differentially-expressed in response to salt stress in the salt-tolerant Sri Lankan rice variety, At354. Two cDNA libraries were constructed from mRNA of shoot samples of salt-stressed (100 mM NaCl) At354 at Phase I and Phase II (24 hours and 10 days, respectively after increasing salt stress up to 100 mM) of salt stress development. A total of 3192 and 960 cDNA clones respectively were screened from Phase I and II libraries. Differential hybridization of the cDNA clones with probes prepared from salt-stressed and unstressed At354 shoot samples enabled identification of up and down-regulated genes in response to salt stress in Phase I and Phase II. The identified, differentially-expressed cDNA clones were re-confirmed by another round of differential hybridization and through Northern hybridization by the RNA dot blot method. Relative reverse transcription polymerase chain reaction (RT-PCR) was performed to compare the expression levels of selected differentially-expressed genes. Sequencing and subsequent homology search in databases identified 14 up-regulated genes and 17 down-regulated genes during Phase I in At354. Similarly, 11 up-regulated genes and 2 down-regulated genes were identified during Phase II. Possible functions of the identified, differentially-expressed genes in conferring salt tolerance in At354 is discussed extensively. These genes may enable exploration of newer avenues for engineering salt tolerance in rice.
引用
收藏
页码:93 / 112
页数:20
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