Zhao Ming-Wen, Liang Wan-Qi, Zhang Da-Bing, Wang Nan, Wang Chen-Guang, Pan Ying-Jie
College of Life Sciences, Nanjing Agricultural University, Key Laboratory of Microbiological Engineering of Agricultural Environment, Ministry of Agriculture, Nanjing 210095, Jiangsu, PR China.
J Microbiol Biotechnol. 2007 Jul;17(7):1106-12.
This report provides the complete nucleotide sequences of the full-length cDNA encoding squalene synthase (SQS) and its genomic DNA sequence from a triterpene-producing fungus, Ganoderma lucidum. The cDNA of the squalene synthase (SQS) (GenBank Accession Number: DQ494674) was found to contain an open reading frame (ORF) of 1,404 bp encoding a 468-amino-acid polypeptide, whereas the SQS genomic DNA sequence (GenBank Accession Number: DQ494675) consisted of 1,984 bp and contained four exons and three introns. Only one gene copy was present in the G lucidum genome. The deduced amino acid sequence of Ganoderma lucidum squalene synthase (Gl-SQS) exhibited a high homology with other fungal squalene synthase genes and contained six conserved domains. A phylogenetic analysis revealed that G. lucidum SQS belonged to the fungi SQS group, and was more closely related to the SQS of U. maydis than to those of other fungi. A gene expression analysis showed that the expression level was relatively low in mycelia incubated for 12 days, increased after 14 to 20 days of incubation, and reached a relatively high level in the mushroom primordia. Functional complementation of Gl-SQS in a SQS-deficient strain of Saccharomyces cerevisiae confirmed that the cloned cDNA encoded a squalene synthase.
本报告提供了来自三萜类化合物产生真菌灵芝的、编码鲨烯合酶(SQS)的全长cDNA的完整核苷酸序列及其基因组DNA序列。发现鲨烯合酶(SQS)的cDNA(GenBank登录号:DQ494674)包含一个1404 bp的开放阅读框(ORF),编码一个468个氨基酸的多肽,而SQS基因组DNA序列(GenBank登录号:DQ494675)由1984 bp组成,包含四个外显子和三个内含子。灵芝基因组中仅存在一个基因拷贝。灵芝鲨烯合酶(Gl-SQS)推导的氨基酸序列与其他真菌鲨烯合酶基因具有高度同源性,并包含六个保守结构域。系统发育分析表明,灵芝SQS属于真菌SQS组,与玉米黑粉菌的SQS关系比与其他真菌的SQS关系更密切。基因表达分析表明,在培养12天的菌丝体中表达水平相对较低,在培养14至20天后升高,并在蘑菇原基中达到相对较高水平。在酿酒酵母的SQS缺陷菌株中对Gl-SQS进行功能互补,证实克隆的cDNA编码一种鲨烯合酶。