Yang Hong, Li Ying, Guan Guo-Hua, Li Xiu-Yu
College of Biological Sciences, China Agricultural University, Beijing 100094, China.
Yi Chuan Xue Bao. 2004 Feb;31(2):166-70.
In order to elucidate the mechanism of fungal heterokayosis, a wild type strain of Fusarium oxysporum f. sp. vasinfectum was isolated from the cotton field in Anyang, Henan Province. Through single hyphal-tip isolation, a heterokaryon, Ag149, was obtained, and its two different phenotypic segregants, Ag149-I and Ag149-III, were separated from the mutated sectors on colony of the heterokaryon. They have remarkable differences on color of colony, morphology of hypha and pathogenicity. After analyzing by RAPD on their nuclear DNA with 100 random primers, no polymorphic difference was found among them. On going to find the different expressed gene, the mRNA differential display method was performed. Two kinds of reverse transcriptase AMV and MMLV, and a kit which consists of three kinds of 3' terminal anchor primers and eight kinds of 5' terminal arbitrary primers were used in differential display PCR (DD-PCR). Total RNA as template was reverse transcribed into corresponding cDNA by 3' terminal anchor primers, and the cDNA were amplified by polymerase chain reaction with a set of one same 3' anchor primer and one 5' arbitrary primer. The PCR products were then resolved on denaturing polyacylamimide gel, and the cDNA bands were visualized by silver staining. Among the 144 PCR products, 19 differentially expressed cDNA fragments ranged from 300 bp to 700 bp were purified. All of them were ligated to pGEM-T vector respectively for sequencing and Rev-Northern blotting. Two cDNA fragments (G5 and C6) were observed to be positive after Rev-Northern blotting. The C6 was highly expressed in the heterokaryon Ag149 and its segregant Ag149-I. It is 564 bp in length and can be predicted 77 amino acids from the beginning of the 3rd to 233th base, and then searched from GenBank. The amino acid sequence of C6 shared homologies with the 6th subunit of NADH dehydrogenase found in some bacteria, plants and animals at 30% - 70% level. While the G5 was highly expressed in Ag149 and its segregant Ag149-III. It is 432 bp in length and can be predicted 101 amino acids from the beginning of the 2nd to 304th base, and the amino acid sequence is 35% homologies comparing with the tetracycline efflux protein (OtrB) of Streptomyces rimosus. We also checked these two kinds of the pGEM-T vector harboring cDNA fragments (C6 and G5) by Southern blotting with their nuclear DNA and mitochondrial DNA (mtDNA) separately. The positive identification signals only appeared from nuclear DNA,and it addressed that C6 and G5 locate on their nuclear genome. The result indicated that the difference between the heterokaryon and its segregants is distinct on gene transcriptional level. Thus a molecular evidence for the formation of heterokaryon in filamentous fungi was provided.
为阐明真菌异核现象的机制,从河南省安阳市棉田分离出尖孢镰刀菌枯萎专化型野生型菌株。通过单菌丝尖端分离,获得了一个异核体Ag149,并从该异核体菌落的突变扇形区域分离出其两个不同表型的分离物Ag149-I和Ag149-III。它们在菌落颜色、菌丝形态和致病性方面有显著差异。用100个随机引物对其核DNA进行RAPD分析后,未发现它们之间存在多态性差异。为寻找差异表达基因,采用了mRNA差异显示法。在差异显示PCR(DD-PCR)中使用了两种逆转录酶AMV和MMLV,以及一套由三种3'端锚定引物和八种5'端任意引物组成的试剂盒。以总RNA为模板,通过3'端锚定引物逆转录成相应的cDNA,然后用一组相同的3'锚定引物和一种5'任意引物通过聚合酶链反应扩增cDNA。PCR产物随后在变性聚丙烯酰胺凝胶上进行分离,cDNA条带通过银染进行可视化。在144个PCR产物中,纯化出19个差异表达的cDNA片段,长度在300 bp至700 bp之间。将它们全部分别连接到pGEM-T载体上进行测序和反向Northern杂交。反向Northern杂交后观察到两个cDNA片段(G5和C6)呈阳性。C6在异核体Ag149及其分离物Ag149-I中高表达。它长度为564 bp,从第3个碱基到第233个碱基开始可预测77个氨基酸,然后在GenBank中进行搜索。C6的氨基酸序列与一些细菌、植物和动物中发现的NADH脱氢酶第6亚基有30% - 70%的同源性。而G5在Ag149及其分离物Ag149-III中高表达。它长度为432 bp,从第2个碱基到第304个碱基开始可预测101个氨基酸,其氨基酸序列与龟裂链霉菌的四环素外排蛋白(OtrB)有35%的同源性。我们还分别用它们的核DNA和线粒体DNA(mtDNA)通过Southern杂交检测了这两种携带cDNA片段(C6和G5)的pGEM-T载体。阳性鉴定信号仅出现在核DNA中,这表明C6和G5位于它们的核基因组上。结果表明,异核体与其分离物在基因转录水平上存在明显差异。从而为丝状真菌中异核体的形成提供了分子证据。