Hey Peter, Robson Geoff, Birch Mike, Bromley Mike
F2G Ltd, Lankro Way, Eccles, Manchester M30 OBH, UK; The University of Manchester, Oxford Road, Manchester M13 9PL, UK.
Fungal Genet Biol. 2008 Feb;45(2):117-26. doi: 10.1016/j.fgb.2007.10.009. Epub 2007 Oct 23.
In recent years the filamentous fungus Aspergillus fumigatus has become a significant cause of infection in man and as such has become the focus of much study. It is thought to be the leading mould pathogen in leukaemia and transplant patients and is responsible for mortality in a large number of individuals with immunological disorders. In an attempt to develop molecular mutagenesis tools for assessment of this organism, the genome of A. fumigatus was analysed to identify possible functional transposable elements. An apparently intact Fot1/Pogo type transposon with 65% identity to the active Tan1 element of Aspergillus niger was identified and designated Aft1. Aft1 is a 1.9kb element present in multiple (>20) highly conserved copies. It encodes a 332 amino acid transposase which contains all the functional motifs required for transposition. In addition, the transposase was expressed in cultures grown at 37 degrees C in all three strains assessed and excision analysis suggests Aft1 may be active and of use in transposon tagging experiments. Southern hybridisation patterns indicate that Aft1 is widely distributed amongst clinical isolates of A. fumigatus with considerable variation in genomic localisation. A comprehensive analysis of the genomic localisation of Aft1 in the sequenced strain AF293 show that one insertion is 30 bases upstream of a predicted gene encoding a G-protein coupled receptor. Expression analysis indicates that this gene has been inactivated by the insertion.
近年来,丝状真菌烟曲霉已成为人类感染的重要原因,因此成为众多研究的焦点。它被认为是白血病和移植患者中主要的霉菌病原体,并且导致大量免疫功能紊乱个体死亡。为了开发用于评估这种生物体的分子诱变工具,对烟曲霉的基因组进行了分析,以鉴定可能的功能性转座元件。鉴定出一个与黑曲霉的活性Tan1元件具有65%同一性的明显完整的Fot1/Pogo型转座子,并将其命名为Aft1。Aft1是一个1.9kb的元件,以多个(>20)高度保守的拷贝存在。它编码一种332个氨基酸的转座酶,该转座酶包含转座所需的所有功能基序。此外,在所评估的所有三个菌株中,转座酶在37℃培养的培养物中表达,切除分析表明Aft1可能具有活性,可用于转座子标签实验。Southern杂交模式表明,Aft1广泛分布于烟曲霉的临床分离株中,其基因组定位存在相当大的差异。对测序菌株AF293中Aft1的基因组定位进行的全面分析表明,一个插入位于预测的编码G蛋白偶联受体的基因上游30个碱基处。表达分析表明该基因已因插入而失活。