植物病理学报
植物病理學報
식물병이학보
ACTA PHYTOPATHOLOGICA SINICA
2007年
5期
487-499
,共13页
张永红%屈志鹏%郑文明%王艳飞%徐亮胜%赵杰%黄丽丽%康振生
張永紅%屈誌鵬%鄭文明%王豔飛%徐亮勝%趙傑%黃麗麗%康振生
장영홍%굴지붕%정문명%왕염비%서량성%조걸%황려려%강진생
cDNA文库%表达序列标签(ESTs)%基因表达%萌发夏孢子%小麦条锈菌
cDNA文庫%錶達序列標籤(ESTs)%基因錶達%萌髮夏孢子%小麥條鏽菌
cDNA문고%표체서렬표첨(ESTs)%기인표체%맹발하포자%소맥조수균
cDNA library%ESTs%gene expression%germinated urediospores%Puccinia striiformis
小麦条锈菌(Puccinia striiformis f.sp.tritici)是全世界范围内小麦生产上的重要病原真菌,但是对小麦条锈菌的基因组和基因功能却了解甚少.为了促进小麦条锈菌基因组学的发展和大规模基因发现,我们以噬菌体λTriplEx2为载体,采用SMART技术构建了小麦条锈菌萌发夏孢子的cDNA文库.原始文库的滴度为1.1 ×106 pfu/mL,平均插入片段长度为750 bp.从文库中随机挑取279个cDNA克隆测序,分析发现这些ESTs的平均GC含量为45.08%.通过聚类分析,279个ESTs拼接成31个contigs和80 singletons.BLASTx分析表明,47%的ESTs与GenBank中报道的功能已知或未知蛋白具有相似性.tBLASTx分析表明12个uniseqs与EST数据库中的序列具有相似性,其中9个是来自担子菌的cDNA文库.几个EST与已知的真菌致病相关基因具有高度相似性.RT-PCR分析了几个基因在小麦条锈菌侵染过程中的表达水平.这些结果为小麦条锈菌夏孢子萌发以及侵染寄主过程中的基因表达研究奠定了很好的分子生物学基础.
小麥條鏽菌(Puccinia striiformis f.sp.tritici)是全世界範圍內小麥生產上的重要病原真菌,但是對小麥條鏽菌的基因組和基因功能卻瞭解甚少.為瞭促進小麥條鏽菌基因組學的髮展和大規模基因髮現,我們以噬菌體λTriplEx2為載體,採用SMART技術構建瞭小麥條鏽菌萌髮夏孢子的cDNA文庫.原始文庫的滴度為1.1 ×106 pfu/mL,平均插入片段長度為750 bp.從文庫中隨機挑取279箇cDNA剋隆測序,分析髮現這些ESTs的平均GC含量為45.08%.通過聚類分析,279箇ESTs拼接成31箇contigs和80 singletons.BLASTx分析錶明,47%的ESTs與GenBank中報道的功能已知或未知蛋白具有相似性.tBLASTx分析錶明12箇uniseqs與EST數據庫中的序列具有相似性,其中9箇是來自擔子菌的cDNA文庫.幾箇EST與已知的真菌緻病相關基因具有高度相似性.RT-PCR分析瞭幾箇基因在小麥條鏽菌侵染過程中的錶達水平.這些結果為小麥條鏽菌夏孢子萌髮以及侵染寄主過程中的基因錶達研究奠定瞭很好的分子生物學基礎.
소맥조수균(Puccinia striiformis f.sp.tritici)시전세계범위내소맥생산상적중요병원진균,단시대소맥조수균적기인조화기인공능각료해심소.위료촉진소맥조수균기인조학적발전화대규모기인발현,아문이서균체λTriplEx2위재체,채용SMART기술구건료소맥조수균맹발하포자적cDNA문고.원시문고적적도위1.1 ×106 pfu/mL,평균삽입편단장도위750 bp.종문고중수궤도취279개cDNA극륭측서,분석발현저사ESTs적평균GC함량위45.08%.통과취류분석,279개ESTs병접성31개contigs화80 singletons.BLASTx분석표명,47%적ESTs여GenBank중보도적공능이지혹미지단백구유상사성.tBLASTx분석표명12개uniseqs여EST수거고중적서렬구유상사성,기중9개시래자담자균적cDNA문고.궤개EST여이지적진균치병상관기인구유고도상사성.RT-PCR분석료궤개기인재소맥조수균침염과정중적표체수평.저사결과위소맥조수균하포자맹발이급침염기주과정중적기인표체연구전정료흔호적분자생물학기출.
Puccinia striiformis f. Sp. Tritici is one of the most economically important fungal pathogen of wheat worldwide. However, very little is known about its genome and gene functions, which can be critical for developing the disease management strategies. To provide new impetus for the studies of its functional genomics and discovery of large-scale gene, we generated a cDNA library from germinated urediospores of P.striiformis f. Sp. Tritici. The cDNA library was constructed from total RNA with bacteriophage λTriplEx2 vector by using SMART technology. Analysis of the cDNA library suggested that the titer of unamplified library was 1.1×106 pfu/mL, and the average size of inserts was about 750 bp. A total of 279 randomly selected cDNA clones has been sequenced and analyzed. The average of GC content for the sequenced ESTs was 45.08%. The ESTs were clustered into 31 contigs and 80 singletons to give a set of 111 unisequences.BLASTX analysis revealed that 47% of the ESTs displayed the significant homology to functionally known or unknown genes from GenBank database. tBLASTx analysis suggested that 12 unisequences showed significant similarity to dbEST entries, of which 9 unisequences were from cDNA libraries of other biotrophic basidiomycetes. Several sequenced eDNA clones showed a high homology to known pathogenicity-related genes of plants. Three identified genes were selected for RT-PCR experiments. Results of the analysis displayed that the level of expression were different during the infection process of P. Striiformis on host. It is the indication that the cDNA library from germinated urediospores can provide a useful resource for mining new genes expressed during rust infection.