|Table of Contents|

cDNA Library Construction and Analysis of Differentially Expressedin Roots of Robinia pseudoacacia Induced by Rhizobium 87-1-1(PDF)

《南京师大学报(自然科学版)》[ISSN:1001-4616/CN:32-1239/N]

Issue:
2014年04期
Page:
76-
Research Field:
生命科学
Publishing date:

Info

Title:
cDNA Library Construction and Analysis of Differentially Expressedin Roots of Robinia pseudoacacia Induced by Rhizobium 87-1-1
Author(s):
Zhao YinjuanSun DunpingHan SufenWu Xiaoqin
Southern China Collaborative Innovation Center of Sustainable Forestry,College of Forestry,Nanjing Forestry University,Jiangsu Key Laboratory for Prevention and Management of Invasion Species,Nanjing 210037,China
Keywords:
RhizobiumRobinia pseudoacaciatransfer cellsSSHfunction analysis
PACS:
S718
DOI:
-
Abstract:
To find special genes in transfer cells of Locust which was differentiated from root epidemic cells induced by rhizobium,a forward and reverse suppression subtraction hybridization(SSH)cDNA library were constructed successfully.Using cDNA from the roots of Robinia pseudoacacia induced by rhizobium as the tester and cDNA from roots of Locust untreated as driver seperately,suppression subtraction hybridization libraries was constructed.500 colonies in both libraries were isolated and sequenced.Functions of ESTs were analyzed by blast in NCBI including database Nt,Nr,Swissprot,COG,Interpro and GO after removing repeat and redundancy sequences.725 uniESTs including 385 uniESTs in forward library and 340 uniESTs in reverse library were obtained.The assembling provided a total of 51 contigs and 674 singletons by cluster analyses of the uniESTs.Nucleotide homology searched with Blastn in NCBI non-redundant nucleotide database and 674 uniESTs(93% of total uniESTs)were homologous with known genes.Protein homology searched with Blastx in NCBI non-redundant protein database and 648 uinESTs(89% of total uniESTs)were homologous with known proteins.The results of gene ontology(GO)annotation showed that 369 uinESTs were involved in biological process with 270 times,molecular function with 448 times and cell component with 484 times respectively.Among these ESTs,putative proteins were related to posttranslational modification,transcription factors,cell signals,cell wall/cell membrane/endomembrane system,cytoskeleton and nodulin genes in positive library,and related to growth and metabolites biosynthesis in reverse library.These results were generally consistent with physiological processes when the Robinia pseudoacacia were induced by rhizobium.Such as MYB transcription factor,Vesicle-associated membrane protein could be found in positive library which might be special expression in the transfer cells to aid the understanding of development of transfer cells.

References:

[1] Azhar A Z,Elke S,Christian R R,et al.Homoserine lactones influence the reaction of plants to rhizobia[J].Int J Mol Sci,2013(14):17 122-17 146.
[2]凯莱斯台舍.刺槐[M].王世绩,张敦伦,译.北京:中国科学技术出版社,1993.
[3]Gunning B E S,Pate J S.“Transfer cell” plant cells with wall ingrowths,specialized in relation to short distance transport of solutions—their occurrence,structure and development[J].Protoplasma,1969,68:107-133.
[4]Gunning B E S,Pate J S.Cells with wall ingrowth(transfer cells)in the placenta of ferns[J].Planta,1969,87:271-274.
[5]Gunning B E S.Transfer cells and roles in transport of solutes in plant[J].Sci Prog,1977,64:539-568.
[6]Kang B H,Xiong Y Q,Donna S W,et al.Miniature1-encoded cell wall invertase is essential for assembly and function of wall-in-growth in the maize endosperm transfer cell[J].Plant Physiology,2009,151:1 366-1 376.
[7]Jose’ F G M,Mauro D P,Anna G,et al.Empty pericarp 4 encodes a mitochondrion-targeted pentatricopeptide repeat protein necessary for seed development and plant growth in maize[J].The Plant Cell,2007,19:196-210.
[8]Stefan H,Ruth S,Norbert S,et al.Differential vascularization of nematode-induced feeding sites[J].PNAS,2008,105(34):12 617-12 622.
[9]韩素芬,黄金生,甘习华,等.刺槐根瘤发生的超微结构研究[J].南京林业大学学报:自然科学版,1996,20(4):17-20.
[10]韩素芬,甘习华,黄金生.接种根瘤后刺槐根表皮形态和超微结构的变化[J].林业科学,1998,34(4):109-110.
[11]林树燕,韩素芬.刺槐根瘤形成过程中根外层传递细胞的功能[J].林业科技开发,2003,17(5):20-21.
[12]吴均章,韩素芬.塑料半薄切片法观察豆科植物根表面传递细胞[J].南京林业大学学报:自然科学版,2003,27(2):65-68.
[13]吴均章,韩素芬,甘习华.根瘤菌诱导紫云英根表面传递细胞的观察[J].南京林业大学学报:自然科学版,2004,28(1):81-83.

[14]Cristina B,Joaquín R,Carmen G M,et al.The Promoter of ZmMRP-1,a maize transfer cell-specific transcriptional activator,is induced at solute exchange surfaces and responds to transport demands[J].Planta,2009,229:235-247.
[15]Elisa G,Joaquín R,Yan G,et al.Establishment of cereal endosperm expression domains:identification and properties of a maize transfer cell-specific transcription factor,ZmMRP[J].The Plant Cell,2002,14:599-610.
[16]Nadja B,Claus F,Salome P,et al.A novel DNA binding protein with homology to Myb oncoproteins containing only one repeat can function as a transcriptional activator[J].The EMBO Journal,1994,22:5 383-5 392.
[17]Gregorio H,Serena V,Francesco S,et al.Molecular characterization of BETI,a gene expressed in the endosperm transfer cells of maize[J].The Plant Cell,1995,7:747-757.
[18]Offler C E,McCurdy D W,Patrick J W,et al.Transfer cells:cells specialized for a special purpose[J].Annu Rev Plant Biol,2003,54:431-454.

Memo

Memo:
-
Last Update: 2014-12-31