Identification of the Neurospora crassa mutation un-10 as a point mutation in a gene encoding eukaryotic translation initiation factor 3, subunit B.

M. Kinney, A. Wiest, M. Plamann, K. McCluskey
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引用次数: 2

Abstract

The Neurospora crassa temperature-sensitive mutant known as un-10 has been shown by a map-based complementation approach to be a single nucleotide change in the open reading frame of the eukaryotic translation initiation factor 3b (NCU02208.3). Authors Matthew Kinney, Aric Wiest, Michael Plamann, and Kevin McCluskey This regular paper is available in Fungal Genetics Reports: https://newprairiepress.org/fgr/vol56/iss1/3 6 Fungal Genetics Reports Identification of the Neurospora crassa mutation un-10 as a point mutation in a gene encoding eukaryotic translation initiation factor 3, subunit B. Matthew Kinney, Aric Wiest, Michael Plamann and Kevin McCluskey. Fungal Genetics Stock Center, School of Biological Sciences, University of Missouri-Kansas City Fungal Genetics Reports 56:6-7 The Neurospora crassa temperature-sensitive mutant known as un-10 has been shown by a map-based complementation approach to be a single nucleotide change in the open reading frame of the eukaryotic translation initiation factor 3b (NCU02208.3). ________________________________________________________________________ Inoue and Ishikawa defined a set of non-remediable, temperature-sensitive "unknown" mutants in Neurospora crassa (Inoue and Ishikawa,1970). To this day, the actual gene altered in many of these "unknown" mutants has not been determined. In order to add value to the Fungal Genetics Stock Center collection, we continue to define the genetic defects associated with these temperature-sensitive mutations (McCluskey et al., 2007, Wiest et al., 2008). Using a complementation-based approach, we have identified the mutation in un-10 as a missense mutation in the eIF3b open reading frame. Building on the demonstration by T. Schmidhauser, that cosmids from the pSV50 cosmid library (Vollmer and Yanofsky, 1986) complement the un-10 mutation in strain FGSC 2342 (Wilson, 1990), we had cosmids 10E12, 11D2, 16C5, and 23C1 end-sequenced. Based on this sequence data, the mutation in FGSC 2342 was predicted to be on contig 10 between bases 68,000 and 92,000 (Galagan, et al, 2003). We selected overlapping cosmids spanning this region and tested their ability to complement the un-10 mutation in FGSC 2342 using electroporation-based transformation (Margolin et. al, 2000; Table 1). Cosmid ID Colonies at 37oC (per ug DNA) Hyg Colonies at 24oC (per ug DNA) pLorist6xh 25D10 21 11 pLorist6xh 66B1 <1 7 pLorist6xh 75A9 56 18 pLorist6xh 107D10 24 7 pSV50 10E12 <1 ND pSV50 11D2 0 ND pSV50 23C1 0 ND No DNA 0 ND Table 1. Identification of cosmids that complement un-10 a. Not Done. The pSV50 does not encode hygromycin resistance. Complementation was successful with cosmids 25:D10, 75:A9 and 107:D10 but not 66:B1. There were four open reading frames in the region common to these overlapping cosmid clones: NCU02205.3, NCU02206.3, NCU02207.3 and NCU02208.3. We amplified copies of the genomic DNA for these open reading frames and used them to transform strain 2342 (Table 2). Only PCR product from NCU02208.3 complemented the un-10 mutation. PCR Product Colonies at 37oC (per ug DNA) NCU02205 0 0 NCU02206 0 <1 NCU02207 0 <1 NCU02208 10 13 No DNA 0 0 Table 2. Identification of PCR products that complement un-10 Data from two different replicates Fewer than one transformant colony per microgram of DNA DNA sequence obtained directly from PCR amplified genomic DNA from strain 2342 showed a single T to C transition at position 1411, resulting in a tryptophan to arginine change in amino acid residue 471. This tryptophan residue is conserved among most fungi (Figure 1) and even higher eukaryotes. The orthologous gene in Saccharomyces cerevisae, PRT1, has alleles which confer a temperature-sensitive phenotype (Hanic-Joyce et al, 1987). None of these corresponds to the mutation 1 Kinney et al.: Identification of the Neurospora crassa mutation un-10 as a point Published by New Prairie Press, 2017
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真核翻译起始因子3亚基B基因点突变的鉴定。
基于图谱互补的方法显示,糙神经孢子虫的温度敏感突变体un-10是真核翻译起始因子3b (NCU02208.3)开放阅读框中的单个核苷酸变化。作者Matthew Kinney, Aric Wiest, Michael Plamann和Kevin McCluskey这篇常规论文可在真菌遗传学报告:https://newprairiepress.org/fgr/vol56/iss1/3 6真菌遗传学报告鉴定粗神经孢子虫突变un-10是编码真核翻译起始因子3亚基b的基因的点突变。Matthew Kinney, Aric Wiest, Michael Plamann和Kevin McCluskey。真菌遗传学报告56:6-7基于图谱互补的方法显示,草神经孢子虫的温度敏感突变体un-10在真核翻译启动因子3b (NCU02208.3)的开放阅读框中发生了单核苷酸变化。________________________________________________________________________ 井上和石川定义一组non-remediable,热敏“未知”突变体在粗糙脉孢菌(井上和石川,1970)。直到今天,在这些“未知的”突变体中,实际的基因改变还没有确定。为了增加真菌遗传库存中心收集的价值,我们继续定义与这些温度敏感突变相关的遗传缺陷(McCluskey et al., 2007, Wiest et al., 2008)。使用基于互补的方法,我们已经确定了un-10中的突变是eIF3b开放阅读框中的错义突变。基于T. Schmidhauser的论证,pSV50 cosmid文库中的cosmid (Vollmer和Yanofsky, 1986)与菌株FGSC 2342中的un10突变互补(Wilson, 1990),我们对cosmid 10E12、11D2、16C5和23C1进行了末端测序。根据该序列数据,FGSC 2342的突变预计位于第10组68,000和92,000碱基之间(Galagan等,2003)。我们选择了跨越该区域的重叠cosmids,并使用基于电穿孔的转化测试了它们补充FGSC 2342中un-10突变的能力(Margolin等人,2000;表1)37℃时Cosmid菌落(每微克DNA) 24℃时Hyg菌落(每微克DNA) pLorist6xh 25D10 21 11 pLorist6xh 66B1 < 17 pLorist6xh 75a56 18 pLorist6xh 107D10 24 7 pSV50 10E12 <1 ND pSV50 11D2 0 ND pSV50 23C1 0 ND No DNA 0 ND识别与un- 10a互补的宇宙。尚未完成。pSV50不编码潮霉素抗性。与25:D10、75:A9和107:D10互补成功,但66:B1不成功。该区域共有4个开放阅读框:NCU02205.3、NCU02206.3、NCU02207.3和NCU02208.3。我们扩增了这些开放阅读框的基因组DNA拷贝,并用它们转化菌株2342(表2)。只有NCU02208.3的PCR产物补充了un-10突变。37℃时PCR产物菌落(每微克DNA) NCU02205 0 0 NCU02206 0 <1 NCU02207 0 <1 NCU02208 10 13 No DNA 0 0表2。从菌株2342的基因组DNA中直接获得的DNA序列显示,在1411位置有一个单T到C的转变,导致氨基酸残基471中色氨酸到精氨酸的变化。这种色氨酸残基在大多数真菌(图1)和更高级的真核生物中是保守的。酿酒酵母的同源基因PRT1具有赋予温度敏感表型的等位基因(Hanic-Joyce et al, 1987)。这些都不对应于突变1 Kinney等人:鉴定粗神经孢子虫突变un-10作为一个点,新草原出版社出版,2017
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