Kubicek Christian P, Baker Scott, Gamauf Christian, Kenerley Charles M, Druzhinina Irina S
Research Area of Gene Technology and Applied Biochemistry, Institute of Chemical Engineering, Vienna University of Technology, Getreidemarkt 9-1665, A-1060 Vienna, Austria.
BMC Evol Biol. 2008 Jan 10;8:4. doi: 10.1186/1471-2148-8-4.
Hydrophobins are proteins containing eight conserved cysteine residues that occur uniquely in mycelial fungi. Their main function is to confer hydrophobicity to fungal surfaces in contact with air or during attachment of hyphae to hydrophobic surfaces of hosts, symbiotic partners or themselves resulting in morphogenetic signals. Based on their hydropathy patterns and solubility characteristics, hydrophobins are divided into two classes (I and II), the latter being found only in ascomycetes.
We have investigated the mechanisms driving the evolution of the class II hydrophobins in nine species of the mycoparasitic ascomycetous genus Trichoderma/Hypocrea, using three draft sequenced genomes (H. jecorina = T. reesei, H. atroviridis = T. atroviride; H. virens = T. virens) an additional 14,000 ESTs from six other Trichoderma spp. (T. asperellum, H. lixii = T. harzianum, T. aggressivum var. europeae, T. longibrachiatum, T. cf. viride). The former three contained six, ten and nine members, respectively. Ten is the highest number found in any ascomycete so far. All the hydrophobins we examined had the conserved four beta-strands/one helix structure, which is stabilized by four disulfide bonds. In addition, a small number of these hydrophobins (HFBs)contained an extended N-terminus rich in either proline and aspartate, or glycine-asparagine. Phylogenetic analysis reveals a mosaic of terminal clades containing duplicated genes and shows only three reasonably supported clades. Calculation of the ratio of differences in synonymous vs. non-synonymous nucleotide substitutions provides evidence for strong purifying selection (KS/Ka >> 1). A genome database search for class II HFBs from other ascomycetes retrieved a much smaller number of hydrophobins (2-4) from each species, and most were from Sordariomycetes. A combined phylogeny of these sequences with those of Trichoderma showed that the Trichoderma HFBs mostly formed their own clades, whereas those of other Sordariomycetes occurred in shared clades.
Our study shows that the genus Trichoderma/Hypocrea has a proliferated arsenal of class II hydrophobins which arose by birth-and-death evolution followed by purifying selection.
疏水蛋白是一类含有八个保守半胱氨酸残基的蛋白质,仅存在于丝状真菌中。它们的主要功能是使真菌与空气接触的表面具有疏水性,或者在菌丝附着于宿主、共生伙伴或其自身的疏水表面时赋予疏水性,从而产生形态发生信号。根据其亲水性模式和溶解性特征,疏水蛋白分为两类(I类和II类),后者仅在子囊菌中发现。
我们利用三个草图测序基因组(嗜绿木霉=里氏木霉,暗绿木霉=深绿木霉;绿木霉=绿色木霉)以及来自其他六种木霉属物种(棘孢木霉、里氏木霉=哈茨木霉、欧洲侵袭木霉变种、长枝木霉、近似绿色木霉)的另外14000条EST序列,研究了木霉属/肉座菌属这9种真菌寄生子囊菌中II类疏水蛋白的进化机制。前三个基因组分别包含6个、10个和9个成员。10个是迄今为止在任何子囊菌中发现的最高数量。我们检测的所有疏水蛋白都具有保守的四股β链/一个螺旋结构,该结构由四个二硫键稳定。此外,这些疏水蛋白(HFBs)中的少数含有富含脯氨酸和天冬氨酸或甘氨酸-天冬酰胺的延伸N端。系统发育分析揭示了包含重复基因的末端分支镶嵌图,并且仅显示出三个得到合理支持的分支。同义核苷酸替换与非同义核苷酸替换差异比率的计算为强烈的纯化选择(KS/Ka>>1)提供了证据。对来自其他子囊菌的II类HFBs进行基因组数据库搜索,每个物种检索到的疏水蛋白数量要少得多(2-4个),并且大多数来自粪壳菌纲。这些序列与木霉序列的联合系统发育分析表明,木霉HFBs大多形成了它们自己的分支,而其他粪壳菌纲的HFBs则出现在共享分支中。
我们的研究表明,木霉属/肉座菌属拥有大量通过生死进化随后进行纯化选择而产生的II类疏水蛋白。