Transcription of purine transporter genes is activated during the isotropic growth phase of Aspergillus nidulans conidia

被引:41
作者
Amillis, S
Cecchetto, G
Sophianopoulou, V
Koukaki, M
Scazzocchio, C
Diallinas, G [1 ]
机构
[1] Univ Athens, Fac Biol, Dept Bot, Athens 15781, Greece
[2] Univ Republica, Unidad Asociada Fac Ciencias, Montevideo, Uruguay
[3] Univ Paris 11, CNRS, UMR C8621, Inst Genet & Microbiol, F-91405 Orsay, France
[4] Natl Ctr Sci Res Demokritos, Inst Biol, Athens 15310, Greece
关键词
D O I
10.1046/j.1365-2958.2003.03956.x
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
Aspergillus nidulans possesses three well-characterized purine transporters encoded by the genes uapA, uapC and azgA. Expression of these genes in mycelium is induced by purines and repressed by ammonium or glutamine through the action of the pathway-specific UaY regulator and the general GATA factor AreA respectively. Here, we describe the regulation of expression of purine transporters during conidiospore germination and the onset of mycelium development. In resting conidiospores, mRNA steady-state levels of purine transporter genes and purine uptake activities are undetectable or very low. Both mRNA steady-state levels and purine transport activities increase substantially during the isotropic growth phase of conidial germination. Both processes occur in the absence of purine induction and independently of the nitrogen source present in the medium. The transcriptional activator UaY is dispensable for the germination-induced expression of the three transporter genes. AreA, on the other hand, is essential for the expression of uapA, but not for that of azgA or uapC, during germination. Transcriptional activation of uapA, uapC and azgA during germination is also independent of the presence of a carbon source in the medium. This work establishes the presence of a novel system triggering purine transporter transcription during germination. Similar results have been found in studies on the expression of other transporters in A. nidulans, suggesting that global expression of transporters might operate as a general system for sensing solute availability.
引用
收藏
页码:205 / 216
页数:12
相关论文
共 37 条
[1]   Substitution F569S converts UapA, a specific uric acid-xanthine transporter, into a broad specificity transporter for purine-related solutes [J].
Amillis, S ;
Koukaki, M ;
Diallinas, G .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 313 (04) :765-774
[2]   NITROGEN METABOLITE REPRESSION IN ASPERGILLUS-NIDULANS [J].
ARST, HN ;
COVE, DJ .
MOLECULAR & GENERAL GENETICS, 1973, 126 (02) :111-141
[3]   MACROMOLECULAR COMPOSITION AND NUCLEAR DIVISION DURING SPORE GERMINATION IN ASPERGILLUS-NIDULANS [J].
BAINBRIDGE, BW .
JOURNAL OF GENERAL MICROBIOLOGY, 1971, 66 (JUN) :319-+
[4]   NITRATE UPTAKE IN ASPERGILLUS-NIDULANS AND INVOLVEMENT OF THE 3RD GENE OF THE NITRATE ASSIMILATION GENE-CLUSTER [J].
BROWNLEE, AG ;
ARST, HN .
JOURNAL OF BACTERIOLOGY, 1983, 155 (03) :1138-1146
[5]  
CECCHETTO G, 2004, IN PRESS J BIOL CHEM
[6]  
COOK R, 1978, BIOCHIM BIOPHYS ACTA, V113, P51
[8]   USE OF ANALOGUES AND SUBSTRATE-SENSITIVITY OF MUTANTS IN ANALYSIS OF PURINE UPTAKE AND BREAKDOWN IN ASPERGILLUS NIDULANS [J].
DARLINGTON, AJ ;
SCAZZOCCHIO, C .
JOURNAL OF BACTERIOLOGY, 1967, 93 (03) :937-+
[9]  
de Koning H, 2000, MOL MEMBR BIOL, V17, P75
[10]   Fungal spore germination: Insights from the molecular genetics of Aspergillus nidulans and Neurospora crassa [J].
dEnfert, C .
FUNGAL GENETICS AND BIOLOGY, 1997, 21 (02) :163-172