• 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

仓鼠细胞突变体中低密度脂蛋白受体的异常形式,这些突变体的受体结构基因存在缺陷。

Unusual forms of low density lipoprotein receptors in hamster cell mutants with defects in the receptor structural gene.

作者信息

Kozarsky K F, Brush H A, Krieger M

出版信息

J Cell Biol. 1986 May;102(5):1567-75. doi: 10.1083/jcb.102.5.1567.

DOI:10.1083/jcb.102.5.1567
PMID:3517003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2114229/
Abstract

The structure and processing of low density lipoprotein (LDL) receptors in wild-type and LDL receptor-deficient mutant Chinese hamster ovary cells was examined using polyclonal anti-receptor antibodies. As previously reported for human LDL receptors, the LDL receptors in wild-type Chinese hamster ovary cells were synthesized as precursors which were extensively processed by glycosylation to a mature form. In the course of normal receptor turnover, an apparently unglycosylated portion of the cysteine-rich N-terminal LDL binding domain of the receptor is proteolytically removed. The LDL receptor-deficient mutants fall into four complementation groups, ldlA, ldlB, ldlC, and ldlD; results of the analysis of ldlB, ldlC, and ldlD mutants are described in the accompanying paper (Kingsley, D. M., K. F. Kozarsky, M. Segal, and M. Krieger, 1986, J. Cell. Biol, 102:1576-1585). Analysis of ldlA cells has identified three classes of mutant alleles at the ldlA locus: null alleles, alleles that code for normally processed receptors that cannot bind LDL, and alleles that code for abnormally processed receptors. The abnormally processed receptors were continually converted to novel unstable intracellular intermediates. We also identified a compound-heterozygous mutant and a heterozygous revertant which indicate that the ldlA locus is diploid. In conjunction with other genetic and biochemical data, the finding of multiple mutant forms of the LDL receptor in ldlA mutants, some of which appeared together in the same cell, confirm that the ldlA locus is the structural gene for the LDL receptor.

摘要

利用多克隆抗受体抗体,对野生型和低密度脂蛋白(LDL)受体缺陷型突变体中国仓鼠卵巢细胞中LDL受体的结构和加工过程进行了检测。正如先前关于人类LDL受体的报道,野生型中国仓鼠卵巢细胞中的LDL受体以前体形式合成,该前体通过糖基化被广泛加工成成熟形式。在正常受体周转过程中,受体富含半胱氨酸的N端LDL结合域中一个明显未糖基化的部分被蛋白酶水解去除。LDL受体缺陷型突变体分为四个互补组,即ldlA、ldlB、ldlC和ldlD;ldlB、ldlC和ldlD突变体的分析结果在随附论文中有所描述(金斯利,D.M.,K.F.科扎尔斯基,M.西格尔,和M.克里格,1986,《细胞生物学杂志》,102:1576 - 1585)。对ldlA细胞的分析在ldlA位点鉴定出三类突变等位基因:无效等位基因、编码正常加工但不能结合LDL的受体的等位基因,以及编码异常加工受体的等位基因。异常加工的受体不断转化为新的不稳定细胞内中间体。我们还鉴定出一个复合杂合突变体和一个杂合回复体,这表明ldlA位点是二倍体。结合其他遗传和生化数据,在ldlA突变体中发现多种LDL受体突变形式,其中一些出现在同一细胞中,证实ldlA位点是LDL受体的结构基因。

相似文献

1
Unusual forms of low density lipoprotein receptors in hamster cell mutants with defects in the receptor structural gene.仓鼠细胞突变体中低密度脂蛋白受体的异常形式,这些突变体的受体结构基因存在缺陷。
J Cell Biol. 1986 May;102(5):1567-75. doi: 10.1083/jcb.102.5.1567.
2
Receptor-mediated endocytosis of low density lipoprotein: somatic cell mutants define multiple genes required for expression of surface-receptor activity.低密度脂蛋白的受体介导内吞作用:体细胞突变体定义了表面受体活性表达所需的多个基因。
Proc Natl Acad Sci U S A. 1984 Sep;81(17):5454-8. doi: 10.1073/pnas.81.17.5454.
3
Three types of low density lipoprotein receptor-deficient mutant have pleiotropic defects in the synthesis of N-linked, O-linked, and lipid-linked carbohydrate chains.三种低密度脂蛋白受体缺陷型突变体在N-连接、O-连接和脂连接碳水化合物链的合成中存在多效性缺陷。
J Cell Biol. 1986 May;102(5):1576-85. doi: 10.1083/jcb.102.5.1576.
4
A new class mutation of low density lipoprotein receptor with altered carbohydrate chains.一种具有改变的糖链的新型低密度脂蛋白受体突变
J Biol Chem. 1988 Dec 25;263(36):19286-9.
5
LDLC encodes a brefeldin A-sensitive, peripheral Golgi protein required for normal Golgi function.低密度脂蛋白胆固醇(LDLC)编码一种对布雷菲德菌素A敏感的外周高尔基体蛋白,该蛋白是正常高尔基体功能所必需的。
J Cell Biol. 1994 Nov;127(3):679-91. doi: 10.1083/jcb.127.3.679.
6
Characterization of a family of gamma-ray-induced CHO mutants demonstrates that the ldlA locus is diploid and encodes the low-density lipoprotein receptor.一组γ射线诱导的中国仓鼠卵巢细胞(CHO)突变体的特征表明,ldlA基因座是二倍体,并且编码低密度脂蛋白受体。
Mol Cell Biol. 1986 Sep;6(9):3268-77. doi: 10.1128/mcb.6.9.3268-3277.1986.
7
Isolation of three classes of conditional lethal Chinese hamster ovary cell mutants with temperature-dependent defects in low density lipoprotein receptor stability and intracellular membrane transport.分离出三类条件致死性中国仓鼠卵巢细胞突变体,它们在低密度脂蛋白受体稳定性和细胞内膜运输方面存在温度依赖性缺陷。
J Biol Chem. 1994 Aug 19;269(33):20958-70.
8
Use of radiation suicide to isolate constitutive and temperature-sensitive conditional Chinese hamster ovary cell mutants with defects in the endocytosis of low density lipoprotein.利用辐射自杀法分离低密度脂蛋白内吞缺陷的组成型和温度敏感型条件性中国仓鼠卵巢细胞突变体。
J Biol Chem. 1991 Dec 15;266(35):24025-30.
9
Isolation and characterization of an extragenic suppressor of the low-density lipoprotein receptor-deficient phenotype of a Chinese hamster ovary cell mutant.中国仓鼠卵巢细胞突变体低密度脂蛋白受体缺陷表型的一个基因外抑制子的分离与鉴定
Mol Cell Biol. 1989 Nov;9(11):4799-806. doi: 10.1128/mcb.9.11.4799-4806.1989.
10
Low binding capacity and altered O-linked glycosylation of low density lipoprotein receptor in a monensin-resistant mutant of Chinese hamster ovary cells.中国仓鼠卵巢细胞莫能菌素抗性突变体中低密度脂蛋白受体的低结合能力及O-连接糖基化改变
J Biol Chem. 1987 Sep 25;262(27):13299-308.

引用本文的文献

1
Defective mucin-type glycosylation on α-dystroglycan in COG-deficient cells increases its susceptibility to bacterial proteases.COG 缺陷细胞中 α- dystroglycan 的粘蛋白型糖基化缺陷增加了其对细菌蛋白酶的易感性。
J Biol Chem. 2018 Sep 14;293(37):14534-14544. doi: 10.1074/jbc.RA118.003014. Epub 2018 Jul 26.
2
Conserved Oligomeric Golgi and Neuronal Vesicular Trafficking.保守寡聚高尔基体与神经元囊泡运输
Handb Exp Pharmacol. 2018;245:227-247. doi: 10.1007/164_2017_65.
3
Mutational and functional analysis of Large in a novel CHO glycosylation mutant.新型CHO糖基化突变体中Large的突变与功能分析
Glycobiology. 2009 Sep;19(9):971-86. doi: 10.1093/glycob/cwp074. Epub 2009 May 21.
4
Aberrant receptor-mediated endocytosis of Schistosoma mansoni glycoproteins on host lipoproteins.曼氏血吸虫糖蛋白在宿主脂蛋白上异常的受体介导内吞作用。
PLoS Med. 2006 Aug;3(8):e253. doi: 10.1371/journal.pmed.0030253.
5
The COG and COPI complexes interact to control the abundance of GEARs, a subset of Golgi integral membrane proteins.COG和COPI复合物相互作用,以控制高尔基体整合膜蛋白的一个子集——GEARs的丰度。
Mol Biol Cell. 2004 May;15(5):2423-35. doi: 10.1091/mbc.e03-09-0699. Epub 2004 Mar 5.
6
Disruptions in Golgi structure and membrane traffic in a conditional lethal mammalian cell mutant are corrected by epsilon-COP.在一个条件致死性哺乳动物细胞突变体中,高尔基体结构和膜运输的破坏可通过ε-COP得到纠正。
J Cell Biol. 1994 Jun;125(6):1213-24. doi: 10.1083/jcb.125.6.1213.
7
LDLC encodes a brefeldin A-sensitive, peripheral Golgi protein required for normal Golgi function.低密度脂蛋白胆固醇(LDLC)编码一种对布雷菲德菌素A敏感的外周高尔基体蛋白,该蛋白是正常高尔基体功能所必需的。
J Cell Biol. 1994 Nov;127(3):679-91. doi: 10.1083/jcb.127.3.679.
8
A fluorescent lipid analogue can be used to monitor secretory activity and for isolation of mammalian secretion mutants.一种荧光脂质类似物可用于监测分泌活性以及分离哺乳动物分泌突变体。
Mol Biol Cell. 1995 Feb;6(2):135-50. doi: 10.1091/mbc.6.2.135.
9
Characterization of a family of gamma-ray-induced CHO mutants demonstrates that the ldlA locus is diploid and encodes the low-density lipoprotein receptor.一组γ射线诱导的中国仓鼠卵巢细胞(CHO)突变体的特征表明,ldlA基因座是二倍体,并且编码低密度脂蛋白受体。
Mol Cell Biol. 1986 Sep;6(9):3268-77. doi: 10.1128/mcb.6.9.3268-3277.1986.
10
DNA-mediated transfer of a human gene required for low-density lipoprotein receptor expression and for multiple Golgi processing pathways.低密度脂蛋白受体表达及多种高尔基体加工途径所需的人类基因的DNA介导转移。
Mol Cell Biol. 1986 Jul;6(7):2734-7. doi: 10.1128/mcb.6.7.2734-2737.1986.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
The use of intensifying screens or organic scintillators for visualizing radioactive molecules resolved by gel electrophoresis.使用增感屏或有机闪烁体来可视化通过凝胶电泳分离的放射性分子。
Methods Enzymol. 1980;65(1):363-71. doi: 10.1016/s0076-6879(80)65047-2.
3
A dot-immunobinding assay for monoclonal and other antibodies.一种用于单克隆抗体及其他抗体的斑点免疫结合测定法。
Anal Biochem. 1982 Jan 1;119(1):142-7. doi: 10.1016/0003-2697(82)90677-7.
4
Order of events in the yeast secretory pathway.酵母分泌途径中的事件顺序。
Cell. 1981 Aug;25(2):461-9. doi: 10.1016/0092-8674(81)90064-7.
5
Characterization of the oligosaccharides of liver Z variant alpha 1-antitrypsin.肝脏Z变体α1-抗胰蛋白酶寡糖的特性分析
Can J Biochem. 1980 Aug;58(8):644-8. doi: 10.1139/o80-089.
6
Early and late functions associated with the Golgi apparatus reside in distinct compartments.与高尔基体相关的早期和晚期功能存在于不同的区室中。
Proc Natl Acad Sci U S A. 1981 Dec;78(12):7453-7. doi: 10.1073/pnas.78.12.7453.
7
Ethylnitrosourea mutagenesis and the isolation of mutant alleles for specific genes located in the T region of mouse chromosome 17.乙基亚硝基脲诱变以及位于小鼠17号染色体T区域的特定基因的突变等位基因的分离。
Genetics. 1984 Oct;108(2):457-70. doi: 10.1093/genetics/108.2.457.
8
A single mutation in Chinese hamster ovary cells impairs both Golgi and endosomal functions.中国仓鼠卵巢细胞中的单个突变会损害高尔基体和内体功能。
J Cell Biol. 1984 Oct;99(4 Pt 1):1296-308. doi: 10.1083/jcb.99.4.1296.
9
Kinetic defects in the processing of the low density lipoprotein receptor in fibroblasts from WHHL rabbits and a family with familial hypercholesterolemia.WHHL兔及一个家族性高胆固醇血症家族的成纤维细胞中低密度脂蛋白受体加工过程的动力学缺陷
Mol Biol Med. 1983 Oct;1(3):353-67.
10
Evidence for extensive subcellular organization of asparagine-linked oligosaccharide processing and lysosomal enzyme phosphorylation.天冬酰胺连接的寡糖加工和溶酶体酶磷酸化广泛亚细胞组织的证据。
J Biol Chem. 1983 Mar 10;258(5):3159-65.