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Analysis of genes specifically expressed under salt stress in salt-tolerant mutant of rice by using DDRT- PCR technique

机译:利用DDRT-PCR技术分析水稻耐盐突变体在盐胁迫下的特异性表达基因

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摘要

Differential display reverse transcription-PCR (DDRT-PCR) technique was used to identify those genes that are expressed differentially between wild type rice variety 77-170 (Oryza Saliva var Japonica) and its salt-tolerant mutant (M-20) under salt stress. Totally 13 salt-inducible cDNA fragments of 200—600 bp were identified and cloned, and were designated as SIGR1 — SIGR13 (salt-induced gene in rice). Northern blot analysis showed that expression of SIGR6 and SIGR8 was salt-inducible in both wildtype and mutant, and expression of SIGR12 in M-20 Was much higher than that in 77-170 under salt stress. It was also shown that expression of SIGR3, SIGR4, SIGR7, SIGR10 and SIGR13 was salt-inducible, and the genes were highly homologous with Rabid whichwas an ABA-inducible gene of rice. The great potential application of DDRT-PCR technique in plant molecular biology research may promote the investigation of expression of salt-induced protein in rice.
机译:差异显示逆转录PCR(DDRT-PCR)技术用于鉴定在盐胁迫下野生型水稻品种77-170(Oryza Saliva var Japonica)及其耐盐突变体(M-20)之间差异表达的那些基因。 。总共鉴定并克隆了13个200-600 bp的盐诱导性cDNA片段,并将其命名为SIGR1-SIGR13(水稻中的盐诱导基因)。 Northern印迹分析表明,在野生型和突变型中,SIGR6和SIGR8的表达都是盐诱导的,在盐胁迫下,M-20中的SIGR12的表达远高于77-170。还显示出SIGR3,SIGR4,SIGR7,SIGR10和SIGR13的表达是盐诱导的,并且这些基因与稻米的ABA诱导基因Rabid高度同源。 DDRT-PCR技术在植物分子生物学研究中的巨大潜力可能会促进盐诱导的蛋白质在水稻中的表达研究。

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