کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10841987 | 1067908 | 2005 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Construction of a SSH library of Aegiceras corniculatum under salt stress and expression analysis of four transcripts
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کلمات کلیدی
major intrinsic proteinsRT-PCRSSH libraryP5CSSSHMIPSAegiceras corniculatumnHA - NHApIPS - PIPSRelative quantification - اندازه گیری نسبیSalt tolerance - تحمل نمکrapid amplification of cDNA ends - تقویت سریع cDNA به پایان می رسدNa+/H+ antiporter - ضد عفونی کننده Na + / H +Mangrove - مانگروRace - مسابقهSuppressive subtractive hybridization - هیبریداسیون کم مخلوطreverse transcription-polymerase chain reaction - واکنش زنجیره ای رونویسی-پلیمراز معکوسplasma membrane intrinsic proteins - پروتئین های ذاتی غشاء پلاسما
موضوعات مرتبط
علوم زیستی و بیوفناوری
علوم کشاورزی و بیولوژیک
دانش گیاه شناسی
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Construction of a SSH library of Aegiceras corniculatum under salt stress and expression analysis of four transcripts Construction of a SSH library of Aegiceras corniculatum under salt stress and expression analysis of four transcripts](/preview/png/10841987.png)
چکیده انگلیسی
Suppressive subtractive hybridization was used to clone transcripts that showed enhanced expression during salt stress in the leaves of a salt-tolerant mangrove species, Aegiceras corniculatum. cDNAs of freshwater germinated and irrigated seedling were used as driver and cDNAs of 6Â h salt-stress seedling were used as tester. By sequencing the whole SSH library, we got 577 ESTs. Among which, 30 had no significant homology to any previously identified genes. Five hundred and twenty-seven of the remaining 547 ESTs represent singletons. Real-time quantitative RT-PCR analysis of four transcripts' expression pattern showed that all of their transcripts were up-regulated during 24Â h after salt shock. Their sequences showed high homology to the delta 1-pyrroline-5-carboxylate synthetase, Na+/H+ antiporter and plasma membrane intrinsic proteins, respectively. Rapid amplification of cDNA ends (RACE) was used for obtaining full-length cDNAs of AcPIP1 and AcPIP2. Characterization and phylogenetic analyses were then carried out according to their sequences.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Plant Science - Volume 169, Issue 1, July 2005, Pages 147-154
Journal: Plant Science - Volume 169, Issue 1, July 2005, Pages 147-154
نویسندگان
Xinhui Fu, Yelin Huang, Shulin Deng, Renchao Zhou, Guili Yang, Xiaowei Ni, Weijing Li, Suhua Shi,