Transcriptional responses of Paxillus involutus and Betula pendula during formation of ectomycorrhizal root tissue

被引:75
作者
Johansson, T
Le Quéré, A
Ahren, D
Söderström, B
Erlandsson, R
Lundeberg, J
Uhlén, M
Tunlid, A
机构
[1] Lund Univ, Dept Microbial Ecol, SE-22362 Lund, Sweden
[2] Royal Inst Technol, Dept Biotechnol, Stockholm, Sweden
关键词
D O I
10.1094/MPMI.2004.17.2.202
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In order to obtain information on genes specifically expressed in the ectomycorrhizal symbiosis, 3,555 expressed sequence tags (ESTs) were analyzed from a cDNA library constructed from ectomycorrhiza formed between the basidiomycete Paxillus involutus and birch (Betula pendula). cDNA libraries from saprophytically growing fungus (3,964 ESTs) and from axenic plants (2,532 ESTs) were analyzed in parallel. By clustering all the EST obtained, a nonredundant set of 2,284 unique transcripts of either fungal or plant origin were identified. The expression pattern of these genes was analyzed using cDNA microarrays. The analyses showed that the plant and fungus responded to the symbiosis by altering the expression levels of a number of enzymes involved in carbon metabolism. Several plant transcripts with sequence similarities to genes encoding enzymes in the tricarboxylic cycle and electron transport chain were down regulated as compared with the levels in free-living roots. In the fungal partner, a number of genes encoding enzymes in the lipid and secondary metabolism were down regulated in mycorrhiza as compared with the saprophytically growing mycelium. A substantial number of the ESTs analyzed displayed significant sequence similarities to proteins involved in biotic stress responses, but only a few of them showed differential expression in the mycorrhizal tissue, including plant and fungal metallothioneins and a plant defensin homologue. Several of the genes that were differentially expressed in the mycorrhizal root tissue displayed sequence similarity to genes that are known to regulate growth and development of plant roots and fungal hyphae, including transcription factors and Rho-like GTPases.
引用
收藏
页码:202 / 215
页数:14
相关论文
共 61 条
[1]   Cloning, expression, and characterization of the hxk-1 gene from the white truffle Tuber borchii Vittad.:: A first step toward understanding sugar metabolism [J].
Agostini, D ;
Polidori, E ;
Palma, F ;
Ceccaroli, P ;
Saltarelli, R ;
Tonelli, D ;
Stocchi, V .
FUNGAL GENETICS AND BIOLOGY, 2001, 33 (01) :15-23
[2]  
AHREN D, IN PRESS MOL ECOL NO
[3]   The significance of digital gene expression profiles [J].
Audic, S ;
Claverie, JM .
GENOME RESEARCH, 1997, 7 (10) :986-995
[4]   Quantitative analysis of mRNA amplification by in vitro transcription [J].
Baugh, L. R. ;
Hill, A. A. ;
Brown, E. L. ;
Hunter, Craig P. .
NUCLEIC ACIDS RESEARCH, 2001, 29 (05)
[5]   Assessing sequence comparison methods with reliable structurally identified distant evolutionary relationships [J].
Brenner, SE ;
Chothia, C ;
Hubbard, TJP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) :6073-6078
[6]   STRUCTURE AND FUNCTION OF THE ECTOMYCORRHIZAL ASSOCIATION BETWEEN PAXILLUS-INVOLUTUS (BATSCH) FR AND BETULA-PENDULA ROTH .1. DYNAMICS OF MYCORRHIZA FORMATION [J].
BRUN, A ;
CHALOT, M ;
FINLAY, RD ;
SODERSTROM, B .
NEW PHYTOLOGIST, 1995, 129 (03) :487-493
[7]   Laccases and other polyphenol oxidases in ecto- and ericoid mycorrhizal fungi [J].
Burke, RM ;
Cairney, JWG .
MYCORRHIZA, 2002, 12 (03) :105-116
[8]   Identification of genes for lignin peroxidases and manganese peroxidases in ectomycorrhizal fungi [J].
Chen, DM ;
Taylor, AFS ;
Burke, RM ;
Cairney, JWG .
NEW PHYTOLOGIST, 2001, 152 (01) :151-158
[9]   Regulation of the quiescence-induced genes: Quiescin Q6, decorin, and ribosomal protein S29 [J].
Coppock, D ;
Kopman, C ;
Gudas, J ;
Cina-Poppe, DA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 269 (02) :604-610
[10]   COMPARATIVE ANATOMY OF THE HOST-FUNGUS INTERFACE IN MYCORRHIZAS [J].
DEXHEIMER, J ;
PARGNEY, JC .
EXPERIENTIA, 1991, 47 (04) :312-321