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两组相互作用的胶原蛋白在秀丽隐杆线虫的细胞外基质中形成功能不同的亚结构。

Two sets of interacting collagens form functionally distinct substructures within a Caenorhabditis elegans extracellular matrix.

作者信息

McMahon Laura, Muriel Joaquin M, Roberts Brett, Quinn Martyn, Johnstone Iain L

机构信息

The Wellcome Centre for Molecular Parasitology, The University of Glasgow, Anderson College, Glasgow G11 6NU, United Kingdom.

出版信息

Mol Biol Cell. 2003 Apr;14(4):1366-78. doi: 10.1091/mbc.e02-08-0479.

DOI:10.1091/mbc.e02-08-0479
PMID:12686594
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC153107/
Abstract

A ubiquitous feature of collagens is protein interaction, the trimerization of monomers to form a triple helix followed by higher order interactions during the formation of the mature extracellular matrix. The Caenorhabditis elegans cuticle is a complex extracellular matrix consisting predominantly of cuticle collagens, which are encoded by a family of approximately 154 genes. We identify two discrete interacting sets of collagens and show that they form functionally distinct matrix substructures. We show that mutation in or RNA-mediated interference of a gene encoding a collagen belonging to one interacting set affects the assembly of other members of that set, but not those belonging to the other set. During cuticle synthesis, the collagen genes are expressed in a distinct temporal series, which we hypothesize exists to facilitate partner finding and the formation of appropriate interactions between encoded collagens. Consistent with this hypothesis, we find for the two identified interacting sets that the individual members of each set are temporally coexpressed, whereas the two sets are expressed approximately 2 h apart during matrix synthesis.

摘要

胶原蛋白的一个普遍特征是蛋白质相互作用,即单体三聚化形成三螺旋结构,随后在成熟细胞外基质形成过程中发生更高层次的相互作用。秀丽隐杆线虫的角质层是一种复杂的细胞外基质,主要由角质层胶原蛋白组成,这些胶原蛋白由大约154个基因组成的家族编码。我们鉴定出两组离散的相互作用胶原蛋白,并表明它们形成功能不同的基质亚结构。我们发现,编码属于一个相互作用组的胶原蛋白的基因突变或RNA介导的干扰会影响该组其他成员的组装,但不会影响另一组的成员。在角质层合成过程中,胶原蛋白基因以独特的时间序列表达,我们推测这一序列的存在是为了便于寻找伴侣以及编码的胶原蛋白之间形成适当的相互作用。与这一假设一致,我们发现,对于两个已鉴定的相互作用组,每组的各个成员在时间上共表达,而在基质合成过程中,这两组的表达时间相隔约2小时。

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本文引用的文献

1
Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans.摄入细菌表达的双链RNA可在秀丽隐杆线虫中产生特异性且有效的基因干扰。
Gene. 2001 Jan 24;263(1-2):103-12. doi: 10.1016/s0378-1119(00)00579-5.
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Osteogenesis imperfecta: prospects for molecular therapeutics.成骨不全症:分子治疗的前景
Mol Genet Metab. 2000 Sep-Oct;71(1-2):225-32. doi: 10.1006/mgme.2000.3039.
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A disease-associated glycine substitution in BP180 (type XVII collagen) leads to a local destabilization of the major collagen triple helix.BP180(XVII型胶原蛋白)中与疾病相关的甘氨酸替代导致主要胶原三螺旋局部不稳定。
Matrix Biol. 2000 Jul;19(3):223-33. doi: 10.1016/s0945-053x(00)00070-6.
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Cuticle collagen genes. Expression in Caenorhabditis elegans.角质层胶原蛋白基因。在秀丽隐杆线虫中的表达。
Trends Genet. 2000 Jan;16(1):21-7. doi: 10.1016/s0168-9525(99)01857-0.
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Caenorhabditis elegans cuticle: a description of new elements of the fibrous layer.秀丽隐杆线虫的角质层:纤维层新成分的描述
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6
The role of actin filaments in patterning the Caenorhabditis elegans cuticle.肌动蛋白丝在秀丽隐杆线虫表皮图案形成中的作用。
Dev Biol. 1997 Apr 15;184(2):373-84. doi: 10.1006/dbio.1997.8530.
7
cis regulatory requirements for hypodermal cell-specific expression of the Caenorhabditis elegans cuticle collagen gene dpy-7.秀丽隐杆线虫表皮胶原蛋白基因dpy-7的皮下细胞特异性表达的顺式调控要求
Mol Cell Biol. 1997 Apr;17(4):2301-11. doi: 10.1128/MCB.17.4.2301.
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A novel epitope tag system to study protein targeting and organelle biogenesis in Trypanosoma brucei.一种用于研究布氏锥虫中蛋白质靶向和细胞器生物发生的新型表位标签系统。
Mol Biochem Parasitol. 1996 May;77(2):235-9. doi: 10.1016/0166-6851(96)02598-4.
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Temporal reiteration of a precise gene expression pattern during nematode development.线虫发育过程中精确基因表达模式的时间性重复。
EMBO J. 1996 Jul 15;15(14):3633-9.
10
Analysis of mutations in the sqt-1 and rol-6 collagen genes of Caenorhabditis elegans.秀丽隐杆线虫sqt-1和rol-6胶原蛋白基因突变分析。
Genetics. 1993 Dec;135(4):1035-45. doi: 10.1093/genetics/135.4.1035.