• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

粗糙脉孢菌芳基硫酸酯酶结构基因的分子克隆及调控分析

Molecular cloning and regulatory analysis of the arylsulfatase structural gene of Neurospora crassa.

作者信息

Paietta J V

机构信息

Department of Biochemistry, Wright State University, Dayton, Ohio 45435.

出版信息

Mol Cell Biol. 1989 Sep;9(9):3630-7. doi: 10.1128/mcb.9.9.3630-3637.1989.

DOI:10.1128/mcb.9.9.3630-3637.1989
PMID:2528685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC362423/
Abstract

The ars-1+ gene of Neurospora crassa encodes the enzyme arylsulfatase. ars-1+ is in a group of highly regulated sulfur-related structural genes that are expressed under conditions of sulfur limitation and are under coordinate control of the cys-3+ and scon+ regulatory genes. The ars-1+ gene was cloned by chromosome walking from the qa gene cluster, using a lambda library. Cotransformation of an N. crassa ars-1 mutant with the isolated lambda clones and the benomyl resistance gene, followed by assay for arylsulfatase activity, was used to screen for the ars-1+ gene. Further confirmation that the cloned segment mapped to the ars-1+ locus was obtained by restriction-fragment-length polymorphism analysis. Northern (RNA) blot analysis showed that the ars-1+ gene was transcribed to give an mRNA of 2.3 kilobases. In wild-type cells, the ars-1+ transcript was abundant under sulfur-derepressing conditions but absent under repressing conditions. Time course analysis showed that the appearance of ars-1+ message in sulfur-derepressed cultures paralleled the appearance of arylsulfatase enzyme activity. In addition, transcription of ars-1+ was detected only under derepressing conditions in a nuclear transcription assay. In a cys-3 regulatory mutant that was unable to synthesize arylsulfatase (or other sulfur-controlled enzymes), there was no ars-1+ transcript under repressing or derepressing conditions. In a temperature-sensitive cys-3 mutant, the ars-1+ transcript was present only at the permissive growth temperature and under sulfur derepression. A negative regulatory mutant, sconc, displayed both constitutive expression of arylsulfatase enzyme activity and content of ars-1+ message.

摘要

粗糙脉孢菌的ars-1+基因编码芳基硫酸酯酶。ars-1+属于一组高度受调控的与硫相关的结构基因,这些基因在硫限制条件下表达,并受cys-3+和scon+调控基因的协同控制。利用λ文库通过染色体步移从qa基因簇克隆了ars-1+基因。用分离的λ克隆和苯菌灵抗性基因对粗糙脉孢菌ars-1突变体进行共转化,随后检测芳基硫酸酯酶活性,以此筛选ars-1+基因。通过限制性片段长度多态性分析进一步证实克隆片段定位于ars-1+位点。Northern(RNA)印迹分析表明,ars-1+基因转录产生一条2.3千碱基的mRNA。在野生型细胞中,ars-1+转录本在硫去阻遏条件下丰富,但在阻遏条件下不存在。时间进程分析表明,硫去阻遏培养物中ars-1+信息的出现与芳基硫酸酯酶活性的出现平行。此外,在核转录试验中,仅在去阻遏条件下检测到ars-1+的转录。在一个无法合成芳基硫酸酯酶(或其他硫控制酶)的cys-3调控突变体中,在阻遏或去阻遏条件下均无ars-1+转录本。在一个温度敏感的cys-3突变体中,ars-1+转录本仅在允许生长温度和硫去阻遏条件下存在。一个负调控突变体sconc,显示出芳基硫酸酯酶活性和ars-1+信息含量的组成型表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/3e6ae35ef0fa/molcellb00057-0055-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/4a2219a0f190/molcellb00057-0053-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/803af787fd1c/molcellb00057-0054-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/0d50c4c86ccd/molcellb00057-0054-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/578d1ef4e981/molcellb00057-0055-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/75c78f883d51/molcellb00057-0055-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/3e6ae35ef0fa/molcellb00057-0055-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/4a2219a0f190/molcellb00057-0053-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/803af787fd1c/molcellb00057-0054-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/0d50c4c86ccd/molcellb00057-0054-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/578d1ef4e981/molcellb00057-0055-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/75c78f883d51/molcellb00057-0055-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/3e6ae35ef0fa/molcellb00057-0055-c.jpg

相似文献

1
Molecular cloning and regulatory analysis of the arylsulfatase structural gene of Neurospora crassa.粗糙脉孢菌芳基硫酸酯酶结构基因的分子克隆及调控分析
Mol Cell Biol. 1989 Sep;9(9):3630-7. doi: 10.1128/mcb.9.9.3630-3637.1989.
2
Molecular cloning and analysis of the scon-2 negative regulatory gene of Neurospora crassa.粗糙脉孢菌scon - 2负调控基因的分子克隆与分析
Mol Cell Biol. 1990 Oct;10(10):5207-14. doi: 10.1128/mcb.10.10.5207-5214.1990.
3
Molecular cloning and analysis of the regulation of cys-14+, a structural gene of the sulfur regulatory circuit of Neurospora crassa.粗糙脉孢菌硫调节回路结构基因cys-14+的分子克隆及调控分析。
Mol Cell Biol. 1988 Apr;8(4):1504-8. doi: 10.1128/mcb.8.4.1504-1508.1988.
4
Novel mutation causing derepression of several enzymes of sulfur metabolism in Neurospora crassa.导致粗糙脉孢菌中几种硫代谢酶去阻遏的新突变。
J Bacteriol. 1972 Jan;109(1):140-51. doi: 10.1128/jb.109.1.140-151.1972.
5
Production of the CYS3 regulator, a bZIP DNA-binding protein, is sufficient to induce sulfur gene expression in Neurospora crassa.CYS3调节因子是一种bZIP DNA结合蛋白,其产生足以诱导粗糙脉孢菌中硫基因的表达。
Mol Cell Biol. 1992 Apr;12(4):1568-77. doi: 10.1128/mcb.12.4.1568-1577.1992.
6
Molecular cloning and characterization of the cys-3 regulatory gene of Neurospora crassa.粗糙脉孢菌cys-3调控基因的分子克隆与特性分析。
Mol Cell Biol. 1987 Jul;7(7):2506-11. doi: 10.1128/mcb.7.7.2506-2511.1987.
7
Cloning and characterization of scon-3+, a new member of the Neurospora crassa sulfur regulatory system.粗糙脉孢菌硫调节系统新成员scon-3+的克隆与特性分析
Eukaryot Cell. 2002 Dec;1(6):875-83. doi: 10.1128/EC.1.6.875-883.2002.
8
Analysis of the sulfur-regulated control of the cystathionine γ-lyase gene of Neurospora crassa.粗糙脉孢菌胱硫醚γ-裂合酶基因的硫调节控制分析。
BMC Res Notes. 2012 Jul 2;5:339. doi: 10.1186/1756-0500-5-339.
9
Molecular cloning and analysis of the regulation of nit-3, the structural gene for nitrate reductase in Neurospora crassa.粗糙脉孢菌中硝酸还原酶结构基因nit-3调控的分子克隆与分析。
Proc Natl Acad Sci U S A. 1987 Dec;84(23):8243-7. doi: 10.1073/pnas.84.23.8243.
10
cys-3, the positive-acting sulfur regulatory gene of Neurospora crassa, encodes a protein with a putative leucine zipper DNA-binding element.cys-3是粗糙脉孢菌的正向作用硫调节基因,编码一种带有假定亮氨酸拉链DNA结合元件的蛋白质。
Mol Cell Biol. 1989 Mar;9(3):1120-7. doi: 10.1128/mcb.9.3.1120-1127.1989.

引用本文的文献

1
Aspects of the Neurospora crassa Sulfur Starvation Response Are Revealed by Transcriptional Profiling and DNA Affinity Purification Sequencing.通过转录谱分析和 DNA 亲和纯化测序揭示粗糙脉孢菌硫饥饿反应的一些方面。
mSphere. 2021 Oct 27;6(5):e0056421. doi: 10.1128/mSphere.00564-21. Epub 2021 Sep 15.
2
Structural and Mechanistic Analysis of the Choline Sulfatase from Sinorhizobium melliloti: A Class I Sulfatase Specific for an Alkyl Sulfate Ester.苜蓿中华根瘤菌胆碱硫酸酯酶的结构与机制分析:一类特异性作用于烷基硫酸酯的硫酸酯酶
J Mol Biol. 2018 Mar 30;430(7):1004-1023. doi: 10.1016/j.jmb.2018.02.010. Epub 2018 Feb 17.
3

本文引用的文献

1
Transcription in Isolated Wheat Nuclei: I. ISOLATION OF NUCLEI AND ELIMINATION OF ENDOGENOUS RIBONUCLEASE ACTIVITY.小麦核转录:I. 核的分离和内源性核糖核酸酶活性的消除。
Plant Physiol. 1980 Feb;65(2):305-8. doi: 10.1104/pp.65.2.305.
2
Efficient cloning of genes of Neurospora crassa.高效克隆粗糙脉孢菌基因。
Proc Natl Acad Sci U S A. 1986 Jul;83(13):4869-73. doi: 10.1073/pnas.83.13.4869.
3
Demonstration of transcriptional regulation of specific genes by phytochrome action.展示了光敏色素作用对特定基因的转录调控。
Matching the Diversity of Sulfated Biomolecules: Creation of a Classification Database for Sulfatases Reflecting Their Substrate Specificity.
匹配硫酸化生物分子的多样性:创建一个反映硫酸酯酶底物特异性的分类数据库。
PLoS One. 2016 Oct 17;11(10):e0164846. doi: 10.1371/journal.pone.0164846. eCollection 2016.
4
Discovery of a novel iota carrageenan sulfatase isolated from the marine bacterium Pseudoalteromonas carrageenovora.从海洋细菌假交替单胞菌中分离得到一种新型iota 角叉菜胶硫酸酯酶的发现。
Front Chem. 2014 Aug 26;2:67. doi: 10.3389/fchem.2014.00067. eCollection 2014.
5
Sulfur-regulated control of the met-2⁺ gene of Neurospora crassa encoding cystathionine β-lyase.粗糙脉孢菌中编码胱硫醚β-裂合酶的met-2⁺基因的硫调节控制。
BMC Res Notes. 2013 Jul 8;6:259. doi: 10.1186/1756-0500-6-259.
6
Analysis of the sulfur-regulated control of the cystathionine γ-lyase gene of Neurospora crassa.粗糙脉孢菌胱硫醚γ-裂合酶基因的硫调节控制分析。
BMC Res Notes. 2012 Jul 2;5:339. doi: 10.1186/1756-0500-5-339.
7
The transcriptome analysis of early morphogenesis in Paracoccidioides brasiliensis mycelium reveals novel and induced genes potentially associated to the dimorphic process.巴西副球孢子菌菌丝体早期形态发生的转录组分析揭示了可能与双态过程相关的新基因和诱导基因。
BMC Microbiol. 2007 Apr 10;7:29. doi: 10.1186/1471-2180-7-29.
8
Contribution of horizontal gene transfer to the evolution of Saccharomyces cerevisiae.水平基因转移对酿酒酵母进化的贡献。
Eukaryot Cell. 2005 Jun;4(6):1102-15. doi: 10.1128/EC.4.6.1102-1115.2005.
9
Lessons from the genome sequence of Neurospora crassa: tracing the path from genomic blueprint to multicellular organism.粗糙脉孢菌基因组序列的启示:探寻从基因组蓝图到多细胞生物体的历程。
Microbiol Mol Biol Rev. 2004 Mar;68(1):1-108. doi: 10.1128/MMBR.68.1.1-108.2004.
10
Cloning and characterization of scon-3+, a new member of the Neurospora crassa sulfur regulatory system.粗糙脉孢菌硫调节系统新成员scon-3+的克隆与特性分析
Eukaryot Cell. 2002 Dec;1(6):875-83. doi: 10.1128/EC.1.6.875-883.2002.
Proc Natl Acad Sci U S A. 1984 Feb;81(4):1112-6. doi: 10.1073/pnas.81.4.1112.
4
Location of Aryl Sulfatase in Conidia and Young Mycelia of Neurospora crassa.粗糙脉孢菌分生孢子和幼菌丝体中芳基硫酸酯酶的定位
J Bacteriol. 1970 Dec;104(3):1254-65. doi: 10.1128/jb.104.3.1254-1265.1970.
5
Genetic regulation of the qa gene cluster of Neurospora crassa: induction of qa messenger ribonucleic acid and dependency on qa-1 function.粗糙脉孢菌qa基因簇的遗传调控:qa信使核糖核酸的诱导及对qa-1功能的依赖性
Mol Cell Biol. 1981 Sep;1(9):829-35. doi: 10.1128/mcb.1.9.829-835.1981.
6
Lambda replacement vectors carrying polylinker sequences.携带多克隆位点序列的λ置换载体。
J Mol Biol. 1983 Nov 15;170(4):827-42. doi: 10.1016/s0022-2836(83)80190-9.
7
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。
Anal Biochem. 1983 Jul 1;132(1):6-13. doi: 10.1016/0003-2697(83)90418-9.
8
Cloning of the am (glutamate dehydrogenase) gene of Neurospora crassa through the use of a synthetic DNA probe.利用合成DNA探针克隆粗糙脉孢菌的am(谷氨酸脱氢酶)基因。
Gene. 1982 Dec;20(3):387-96. doi: 10.1016/0378-1119(82)90207-4.
9
Chromosomal loci of Neurospora crassa.粗糙脉孢菌的染色体位点。
Microbiol Rev. 1982 Dec;46(4):426-570. doi: 10.1128/mr.46.4.426-570.1982.
10
Regulation of nitrogen metabolism and gene expression in fungi.真菌中氮代谢与基因表达的调控
Microbiol Rev. 1981 Sep;45(3):437-61. doi: 10.1128/mr.45.3.437-461.1981.