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青杄PwPSAF基因的克隆与组织表达分析 被引量:5

Cloning and Tissue Expression Analysis of PwPSAF in Picea wilsonii
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摘要 PSAF是绿色植物光系统Ⅰ反应中心F亚基,在光合作用电子迁移过程中起着重要作用。以青杄cDNA文库为模板,根据PwPSAF的EST序列设计引物,进行5'-RACE和3'-RACE试验,以获得青杄PwPSAF的末端序列,经过与EST序列进行拼接获取青杄PwPSAF的全长cDNA序列。基于其氨基酸序列,利用Expasy tools、DNAMAN、ClustalX和MEGA等工具,进行理化性质、二级结构和三级结构的生物信息学分析。结果表明:PwPSAF是一个由253 aa组成的蛋白质,理论分子量为27.04 kDa,等电点为9.57,预测蛋白有2个跨膜区域,蛋白质的C端具有保守的结构。RT-qPCR试验显示PwPSAF主要在青杄的针叶中表达。在种子萌发过程中吸胀期(0~ 2天)表达量最高,在4天时表达量降低,随着子叶的不断长出,其表达量又逐渐增高。在干旱和盐胁迫下,针叶中的PwPSAF的表达量被大幅下调。研究结果显示PwPSAF在青杄种子萌发及非生物逆境胁迫下的光合过程中起着重要作用。 PSAF is F subunit of photosystem Ⅰ reaction center complex in higher plants and plays an important role during the process of electron mobility of photosynthesis. The full length cDNA of PwPSAF was obtained by RACE PCR assays based on the cDNA library of Picea wilsonii and EST fragment of PwPSAF. Several pieces of software and tools such as Expasy,DNAMAN,ClustalX and MEGA were used to analyze the physical and chemical properties and secondary and tertiary structures of PwPSAF. Expression level of PwPSAF in different tissues of seedlings was identified by RT-qPCR under drought and salt treatments. Furthermore,the expression patterns were investigated at different stages of seed germination. We found that PwPSAF was composed of 253 amino acids and the theoretical molecular weight was 27. 04kDa with isoelectric point of 9. 57. The protein has two transmembrane domains and shares conserved C domain with other species such as Picea sitchensis and Vitis vinifera. RT-qPCR assays indicated that PwPSAF was mainly expressed in needles of Picea wilsonii. During seed germination,PwPSAF showed the highest expression within 2 days after germination,and then declined on the fourth day. With the cotyledons grown,the expression of PwPSAF was up-regulated again. In addition,the expression level of PwPSAF was down-regulated in the needles under drought and salt stresses.These results suggest that PwPSAF in P. wilsonii plays an important role during seed germination and in response to abiotic stresses.
出处 《林业科学》 EI CAS CSCD 北大核心 2013年第10期40-47,共8页 Scientia Silvae Sinicae
基金 国家自然科学基金项目(31270663) 国家转基因生物新品种培育科技重大专项(2011ZX08009-003-002)
关键词 青杄 PSAF 生物信息学分析 组织表达 胁迫响应 Picea wilsonii PSAF bioinformatic analysis tissue-specific expression stress response
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  • 1卜令铎,张仁和,常宇,薛吉全,韩苗苗.苗期玉米叶片光合特性对水分胁迫的响应[J].生态学报,2010,30(5):1184-1191. 被引量:132
  • 2李长江,曹一博,张凌云.青杄PSAK的克隆及生物信息学分析[J].生物技术,2012,22(3):4-9. 被引量:7
  • 3张娟,姜闯道,平吉成.盐胁迫对植物光合作用影响的研究进展[J].农业科学研究,2008,29(3):74-80. 被引量:48
  • 4Agalarov R, Byrdin M, Rappaport F, et al. 2008. Removal of the PsaF polypeptide biases electron transfer in favor of the PsaB branch of cofactors in Triton X-100 photosystem I complexes from Synechococcus sp. PCC 7002. Photochemistry and Photobiology, 84 (6) : 1371 -1380.
  • 5Allakhverdiev S I, Nishiyama Y, Miyairi S, et al. 2002. Salt stress inhibits the repair of photodamaged photosystem Ⅱ by suppressing the transcription and translation of psbA genes in Synechocystis. Plant Physiology, 130 (3) : 1443 -1453.
  • 6Batlang U. 2010. Identification of drought-responsive genes and validation for drought resistance in flee. Virginia Polytechnic Institute and State University. Doctor of Philosophy.
  • 7Berry L L, Brzczowski P, Wilson K E. 2011. Inactivation of the STT7 gene protects PsaF-deficient Chlamydomonas reinhardtii cells from oxidative stress under high light. Physiologia Plantarum, 141 (2) : 188 - 196.
  • 8Chandok M R, Sopory S K, Oelmuller R. 2001. Cytoplasmic kinase and phosphatase activities can induce PsaF gene expression in the absence of functional plastids: evidence that phosphorylation/ dephosphorylation events are involved in interorganellar crosstalk. Molecular & General Genetics: MGG, 264 (6) : 819 -826.
  • 9Chitnis P R, Purvis D, Nelson N. 1991. Molecular cloning and targeted mutagenesis of the gent PsaF encoding subunit Ⅲ of photosystem I from the cyanobactcrium Synechocystis sp. PCC 6803. The Journal of Biological Chemistry, 266 (30): 20146-20151.
  • 10Farah J, Rappaport F, Choquet Y, et al. 1995. Isolation of a psaF- deficient mutant of Chlamydomonas reinhardtii: efficient interaction of plastocyanin with the photosystem Ⅰ reaction center is mediated by the PsaF subunit. The EMBO Journal, 14 (20) : 4976 -4984.

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  • 1Teale WD, Paponov IA, Palme K. Auxin in action : signalling, transport and the control of plant growth and development [ J ] . Nat Rev Mol Cell Biol, 2006, 7 ( 11 ) : 847-859.
  • 2Leyser O. Dynamic integration of auxin transport and signalling [ J ] . Curr Biol, 2006, 16 ( 11 ) : 424-433.
  • 3Quint M, Gray WM. Auxin signalling [J] . Curr Opin Plant Biol, 2006, 9 ( 5 ) : 448-453.
  • 4Chen JG, Shimomura S, Sitbon F, et al. The role of auxin binding protein 1 in the expansion of tobacco leaf cells [ J ] . Plant J, 2001, 28 ( 6 ) : 607-617.
  • 5Timpte C. Auxin binding protein : curiouser and curiouser [ J ] . Trends Plant Sci, 2001, 6 ( 12 ) : 586-590.
  • 6Guilfoyle TJ, HagenG. Auxin response factors : recent advances in auxin biology [ J ] . Plant Growth Regul, 2001, 20 ( 3 ) : 281-291.
  • 7Ulmasov T, Hagen G, Guilfoyle TJ. ARF1, a transcription factor that binds to auxin response elements [ J ]. Science, 1997, 276 ( 5320 ): 1865-1868.
  • 8Ulmasov T, Hagen G, Guilfoyle TJ. Dimerization and DNA binding of auxin response factors [ J ] . Plant J, 1999, 19 ( 3 ) : 309-319.
  • 9Dreher KA, Callis J. Ubiquitin, hormones and biotic stress in plants[J], Annals Bot, 2007, 99 ( 5 ) : 787-822.
  • 10Leyser O. Molecular genetics of auxin signaling [J]. Annu Rev Plant Biol, 2002, ( 53 ) : 377-398.

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