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两个新的依赖S-腺苷甲硫氨酸的甲基转移酶编码基因的鉴定与表征表明它们参与了……的菌柄伸长过程 。 (注:原文中“of”后面缺少具体内容)

Identification and Characterization of Two New S-Adenosylmethionine-Dependent Methyltransferase Encoding Genes Suggested Their Involvement in Stipe Elongation of .

作者信息

Huang Qianhui, Mukhtar Irum, Zhang Yelin, Wei Zhongyang, Han Xing, Huang Rongmei, Yan Junjie, Xie Baogui

机构信息

Mycological Research Center, Fujian Agriculture and Forestry University, Fuzhou, China.

出版信息

Mycobiology. 2019 Sep 13;47(4):441-448. doi: 10.1080/12298093.2019.1658332. eCollection 2019.

Abstract

Two new SAM-dependent methyltransferase encoding genes ( and ) were identified from the genome of . In order to make a comprehensive characterization of both genes, we performed analysis of both genes and used qRT-PCR to reveal their expression patterns during the development of . There are 4 and 6 exons with total length of 693 and 978 bp in and , respectively. The deduced proteins, i.e., FVSMT1 and FVSMT2 contained 325 and 230 amino acids with molecular weight 36297 and 24894 Da, respectively. Both proteins contained a SAM-dependent catalytic domain with signature motifs (I, p-I, II, and III) defining the SAM fold. SAM-dependent catalytic domain is located either in the middle or at the N-terminal of FVSMT2 and FVSMT1, respectively. Alignment and phylogenic analysis showed that FVSMT1 is a homolog to a protein-arginine omega--methyltransferase, while FVSMT2 is of cinnamoyl CoA -methyltransferase type and predicted subcellular locations of these proteins are mitochondria and cytoplasm, respectively. qRT-PCR showed that and expression was regulated in different developmental stages. The maximum expression levels of and were observed in stipe elongation, while no difference was found in mycelium and pileus. These results positively demonstrate that both the methyltransferase encoding genes are involved in the stipe elongation of .

摘要

从[具体物种名称]的基因组中鉴定出两个新的依赖S-腺苷甲硫氨酸(SAM)的甲基转移酶编码基因([基因名称1]和[基因名称2])。为了全面表征这两个基因,我们对这两个基因进行了[具体分析方法]分析,并使用实时定量逆转录聚合酶链式反应(qRT-PCR)来揭示它们在[具体物种名称]发育过程中的表达模式。[基因名称1]和[基因名称2]分别有4个和6个外显子,全长分别为693和978 bp。推导的蛋白质,即FVSMT1和FVSMT2分别包含325和230个氨基酸,分子量分别为36297和24894 Da。两种蛋白质都包含一个依赖SAM的催化结构域,带有定义SAM折叠的特征基序(I、p-I、II和III)。依赖SAM的催化结构域分别位于FVSMT2的中间和FVSMT1的N端。序列比对和系统发育分析表明,FVSMT1是一种蛋白质精氨酸ω-甲基转移酶的同源物,而FVSMT2属于肉桂酰辅酶A O-甲基转移酶类型,这些蛋白质预测的亚细胞定位分别是线粒体和细胞质。qRT-PCR表明,[基因名称1]和[基因名称2]的表达在不同发育阶段受到调控。在菌柄伸长阶段观察到[基因名称1]和[基因名称2]的最高表达水平,而在菌丝体和菌盖中未发现差异。这些结果有力地证明了这两个甲基转移酶编码基因都参与了[具体物种名称]的菌柄伸长过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba1/6968334/baf32abfcb2b/TMYB_A_1658332_F0001_B.jpg

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