• 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

酵母中的蛋白质糖基化:ALG7基因的转录本异质性

Protein glycosylation in yeast: transcript heterogeneity of the ALG7 gene.

作者信息

Kukuruzinska M A, Robbins P W

出版信息

Proc Natl Acad Sci U S A. 1987 Apr;84(8):2145-9. doi: 10.1073/pnas.84.8.2145.

DOI:10.1073/pnas.84.8.2145
PMID:3031666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC304605/
Abstract

The first enzyme in the lipid-linked oligosaccharide biosynthetic pathway, UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (UDP-N-acetyl-D-glucosamine:dolichyl-phosphate-N-acetyl- D-glucosaminephosphotransferase, EC 2.7.8.15), is encoded by the ALG7 gene. We show that this gene is essential for cell growth, since a null mutation constructed with standard gene disruption techniques results in cell lethality. The ALG7 gene is transcribed into two major messages, approximately 1.38 and 1.56 kilobase pairs (kbp) in size, and this heterogeneity has been mapped to the 3' untranslated region. Two sets of tripartite sequences implicated in transcription termination begin 15 bp and 256 bp past the translation stop codon, TGA. The ratios of the two major transcripts change with gene dosage, with the longer mRNA becoming more abundant in cells containing higher levels of the ALG7 gene. Changes in transcript ratios are also observed in mutants defective in lipid-linked sugar-donor biosynthesis. In addition, there is 5' heterogeneity in the ALG7 mRNAs. The transcripts start at four initiation sites located within a 20-bp region. Two potentially functional TATA elements have been identified at positions -157 and -139, which may be involved in initiation from multiple sites. These features point to numerous factors that may be involved in the regulation of the expression of the ALG7 gene.

摘要

脂质连接寡糖生物合成途径中的第一个酶,UDP-N-乙酰葡糖胺-多萜醇磷酸-N-乙酰葡糖胺磷酸转移酶(UDP-N-乙酰-D-葡糖胺:多萜醇磷酸-N-乙酰-D-葡糖胺磷酸转移酶,EC 2.7.8.15),由ALG7基因编码。我们发现该基因对细胞生长至关重要,因为用标准基因破坏技术构建的无效突变会导致细胞死亡。ALG7基因转录为两条主要的mRNA,大小约为1.38和1.56千碱基对(kbp),这种异质性已定位到3'非翻译区。两组与转录终止有关的三联体序列在翻译终止密码子TGA下游15 bp和256 bp处开始。两种主要转录本的比例随基因剂量而变化,在含有较高水平ALG7基因的细胞中,较长的mRNA更为丰富。在脂质连接糖供体生物合成缺陷的突变体中也观察到转录本比例的变化。此外,ALG7 mRNA存在5'端异质性。转录本从位于20 bp区域内的四个起始位点开始。在-157和-139位置已鉴定出两个潜在的功能性TATA元件,它们可能参与多个位点的起始。这些特征表明可能有许多因素参与ALG7基因表达的调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/2fdebf5f4fd3/pnas00273-0046-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/b8f5c3daa46f/pnas00273-0044-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/91a99777fa09/pnas00273-0044-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/a6d4765c7eb3/pnas00273-0045-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/c533d473047d/pnas00273-0045-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/ca514a0c667a/pnas00273-0045-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/6145091a5dc1/pnas00273-0045-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/2fdebf5f4fd3/pnas00273-0046-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/b8f5c3daa46f/pnas00273-0044-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/91a99777fa09/pnas00273-0044-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/a6d4765c7eb3/pnas00273-0045-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/c533d473047d/pnas00273-0045-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/ca514a0c667a/pnas00273-0045-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/6145091a5dc1/pnas00273-0045-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d888/304605/2fdebf5f4fd3/pnas00273-0046-a.jpg

相似文献

1
Protein glycosylation in yeast: transcript heterogeneity of the ALG7 gene.酵母中的蛋白质糖基化:ALG7基因的转录本异质性
Proc Natl Acad Sci U S A. 1987 Apr;84(8):2145-9. doi: 10.1073/pnas.84.8.2145.
2
Deregulation of the first N-glycosylation gene, ALG7, perturbs the expression of G1 cyclins and cell cycle arrest in Saccharomyces cerevisiae.首个N-糖基化基因ALG7的失调会扰乱酿酒酵母中G1期细胞周期蛋白的表达并导致细胞周期停滞。
Biochem Biophys Res Commun. 1997 Aug 28;237(3):562-5. doi: 10.1006/bbrc.1997.7190.
3
Asparagine-linked glycosylation in Saccharomyces cerevisiae: genetic analysis of an early step.酿酒酵母中的天冬酰胺连接的糖基化作用:早期步骤的遗传分析
Mol Cell Biol. 1984 Nov;4(11):2381-8. doi: 10.1128/mcb.4.11.2381-2388.1984.
4
Diminished activity of the first N-glycosylation enzyme, dolichol-P-dependent N-acetylglucosamine-1-P transferase (GPT), gives rise to mutant phenotypes in yeast.首个N-糖基化酶,即多萜醇-P依赖的N-乙酰葡糖胺-1-P转移酶(GPT)活性降低,会在酵母中产生突变表型。
Biochim Biophys Acta. 1995 Feb 22;1247(1):51-9. doi: 10.1016/0167-4838(94)00201-q.
5
A hypomorphic allele of the first N-glycosylation gene, ALG7, causes mitochondrial defects in yeast.首个N-糖基化基因ALG7的一个低表达等位基因会导致酵母中的线粒体缺陷。
Biochim Biophys Acta. 2005 May 25;1723(1-3):33-44. doi: 10.1016/j.bbagen.2005.01.017. Epub 2005 Feb 17.
6
Expression of the first N-glycosylation gene in the dolichol pathway, ALG7, is regulated at two major control points in the G1 phase of the Saccharomyces cerevisiae cell cycle.在酿酒酵母细胞周期的G1期,多萜醇途径中的首个N-糖基化基因ALG7的表达在两个主要控制点受到调控。
Exp Cell Res. 1995 Aug;219(2):477-86. doi: 10.1006/excr.1995.1255.
7
The dual role of mRNA half-lives in the expression of the yeast ALG7 gene.mRNA半衰期在酵母ALG7基因表达中的双重作用。
Mol Cell Biochem. 1997 Apr;169(1-2):95-106. doi: 10.1023/a:1006803004151.
8
AglH, a thermophilic UDP-N-acetylglucosamine-1-phosphate:dolichyl phosphate GlcNAc-1-phosphotransferase initiating protein N-glycosylation pathway in Sulfolobus acidocaldarius, is capable of complementing the eukaryal Alg7.AglH是嗜热栖热菌中启动蛋白质N-糖基化途径的一种嗜热UDP-N-乙酰葡糖胺-1-磷酸:二萜醇磷酸GlcNAc-1-磷酸转移酶,它能够互补真核生物的Alg7。
Extremophiles. 2017 Jan;21(1):121-134. doi: 10.1007/s00792-016-0890-2. Epub 2016 Nov 7.
9
Identification of the archaeal alg7 gene homolog (encoding N-acetylglucosamine-1-phosphate transferase) of the N-linked glycosylation system by cross-domain complementation in Saccharomyces cerevisiae.通过在酿酒酵母中进行跨域互补鉴定N-连接糖基化系统的古菌alg7基因同源物(编码N-乙酰葡糖胺-1-磷酸转移酶)。
J Bacteriol. 2008 Mar;190(6):2217-20. doi: 10.1128/JB.01778-07. Epub 2008 Jan 4.
10
Targeted selection of recombinant clones through gene dosage effects.通过基因剂量效应进行重组克隆的靶向选择。
Proc Natl Acad Sci U S A. 1983 Nov;80(22):6750-4. doi: 10.1073/pnas.80.22.6750.

引用本文的文献

1
ALG13-Related Epilepsy: Current Insights and Future Research Directions.与ALG13相关的癫痫:当前见解与未来研究方向
Neurochem Res. 2024 Dec 14;50(1):60. doi: 10.1007/s11064-024-04300-y.
2
Rft1 catalyzes lipid-linked oligosaccharide translocation across the ER membrane.Rft1 催化脂连接寡糖穿过内质网膜的易位。
Nat Commun. 2024 Jun 17;15(1):5157. doi: 10.1038/s41467-024-48999-3.
3
Evolutionary rescue of phosphomannomutase deficiency in yeast models of human disease.磷酸甘露糖变位酶缺乏症在人类疾病酵母模型中的进化拯救。

本文引用的文献

1
Temperature-sensitive yeast mutants deficient in asparagine-linked glycosylation.缺乏天冬酰胺连接糖基化的温度敏感型酵母突变体。
J Biol Chem. 1982 Mar 25;257(6):3203-10.
2
Synthesis and processing of asparagine-linked oligosaccharides.天冬酰胺连接寡糖的合成与加工
Annu Rev Biochem. 1981;50:555-83. doi: 10.1146/annurev.bi.50.070181.003011.
3
Buffer gradient gels and 35S label as an aid to rapid DNA sequence determination.缓冲液梯度凝胶和35S标记辅助快速DNA序列测定。
Elife. 2022 Oct 10;11:e79346. doi: 10.7554/eLife.79346.
4
The Impact of Glycoengineering on the Endoplasmic Reticulum Quality Control System in Yeasts.糖基工程对酵母内质网质量控制系统的影响
Front Mol Biosci. 2022 Jun 2;9:910709. doi: 10.3389/fmolb.2022.910709. eCollection 2022.
5
Expression, purification, and phylogenetic analysis of MDIS1-INTERACTING RECEPTOR-LIKE KINASE1 (MIK1).MDIS1-INTERACTING RECEPTOR-LIKE KINASE1 (MIK1) 的表达、纯化和系统进化分析。
Protein J. 2020 Oct;39(5):461-471. doi: 10.1007/s10930-020-09926-9. Epub 2020 Oct 26.
6
Plant Leucine-Rich Repeat Receptor Kinase (LRR-RK): Structure, Ligand Perception, and Activation Mechanism.植物类亮氨酸丰富重复受体激酶(LRR-RK):结构、配体感知和激活机制。
Molecules. 2019 Aug 25;24(17):3081. doi: 10.3390/molecules24173081.
7
Reconstitution of the lipid-linked oligosaccharide pathway for assembly of high-mannose N-glycans.重建脂质连接寡糖途径以组装高甘露糖型 N-聚糖。
Nat Commun. 2019 Apr 18;10(1):1813. doi: 10.1038/s41467-019-09752-3.
8
UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase is indispensable for oogenesis, oocyte-to-embryo transition, and larval development of the nematode Caenorhabditis elegans.UDP-N-乙酰氨基葡萄糖-二磷酸岩藻糖基转移酶对于线虫秀丽隐杆线虫的卵子发生、卵母细胞到胚胎的转变和幼虫发育是必不可少的。
Glycobiology. 2019 Feb 1;29(2):163-178. doi: 10.1093/glycob/cwy104.
9
Protein N-glycosylation in oral cancer: dysregulated cellular networks among DPAGT1, E-cadherin adhesion and canonical Wnt signaling.口腔癌中的蛋白质N-糖基化:DPAGT1、E-钙黏蛋白黏附与经典Wnt信号通路之间失调的细胞网络
Glycobiology. 2014 Jul;24(7):579-91. doi: 10.1093/glycob/cwu031. Epub 2014 Apr 17.
10
N-linked protein glycosylation in the endoplasmic reticulum.内质网中的 N-连接蛋白糖基化。
Cold Spring Harb Perspect Biol. 2013 Aug 1;5(8):a013359. doi: 10.1101/cshperspect.a013359.
Proc Natl Acad Sci U S A. 1983 Jul;80(13):3963-5. doi: 10.1073/pnas.80.13.3963.
4
Quantitative assay and subcellular distribution of enzymes acting on dolichyl phosphate in rat liver.大鼠肝脏中作用于磷酸多萜醇的酶的定量测定及亚细胞分布
J Cell Biol. 1981 Dec;91(3 Pt 1):679-88. doi: 10.1083/jcb.91.3.679.
5
Two yeast mutations in glucosylation steps of the asparagine glycosylation pathway.天冬酰胺糖基化途径糖基化步骤中的两个酵母突变。
J Biol Chem. 1984 Jan 10;259(1):412-7.
6
Yeast mutants deficient in protein glycosylation.缺乏蛋白质糖基化的酵母突变体。
Proc Natl Acad Sci U S A. 1983 Dec;80(24):7466-70. doi: 10.1073/pnas.80.24.7466.
7
Transformation of intact yeast cells treated with alkali cations.经碱金属阳离子处理的完整酵母细胞的转化
J Bacteriol. 1983 Jan;153(1):163-8. doi: 10.1128/jb.153.1.163-168.1983.
8
Targeted selection of recombinant clones through gene dosage effects.通过基因剂量效应进行重组克隆的靶向选择。
Proc Natl Acad Sci U S A. 1983 Nov;80(22):6750-4. doi: 10.1073/pnas.80.22.6750.
9
One-step gene disruption in yeast.酵母中的一步基因破坏
Methods Enzymol. 1983;101:202-11. doi: 10.1016/0076-6879(83)01015-0.
10
Transcription terminates in yeast distal to a control sequence.转录在酵母中于一个控制序列远端终止。
Cell. 1983 Jun;33(2):607-14. doi: 10.1016/0092-8674(83)90441-5.