Har-el R, Sharma Y D, Aguilera A, Ueyama N, Wu J J, Eyre D R, Juricić L, Chandrasekaran S, Li M, Nah H D
Department of BioStructure and Function, School of Dental medicine, University of Connecticut Health Center, Farmington 06030.
J Biol Chem. 1992 May 15;267(14):10070-6.
Fibrous and nonfibrous collagens comprise two major groups within the collagen family and both groups are found in a diverse variety of tissue fabrics. Type IX collagen is in the nonfibrous group; three different subunits of type IX collagen have been identified and the alpha 1 and alpha 2 subunits have been cloned. Using molecular cloning methods we have isolated, from an embryonic chicken cartilage library, cDNA clones which code for the entire alpha 3 chain of chicken type IX collagen. The cDNA clones encompass 2416 base pairs which have a conceptual open reading frame for a protein containing 675 amino acids including 193 Gly-X-Y repeats. These collagen repeats are in three separate domains which are interspersed with four major noncollagen domains. The collagen repeats also have four minor interruptions. This chain organization directly aligns with both the alpha 1 and alpha 2 chains of chicken type IX collagen. Comparison of the deduced amino acid sequence with peptide sequences of type IX collagens shows identity with 95 of the 96 known residues of the chicken alpha 3 chain and 81 of the 98 known residues of the bovine alpha 3 chain. The identical residues match those in five peptide fragments, two from the bovine protein and three from the chicken protein. The chicken and bovine alpha 3 chains have conserved cross-linking sites, separated by 137 residues which span 40 nm, the length of the hole zone in a collagen fibril. The NC3 domain of the chicken alpha 3 chain contains a repeat Cys-Pro motif which is present in both vertebrate and invertebrate nonfibrillar collagens. Northern blot hybridization exhibits a major mRNA of about 3.3 kilobases; this transcript is found in cartilaginous tissues in the embryo, including the developing limb and is not detected in other tissues or in the precondensation stage of limb development. The composite data delineate the primary structure of the alpha 3 chain of chicken type IX collagen, show its close relationship to the alpha 1 and alpha 2 chains, demonstrate its mRNA transcript, and show the appearance of that transcript in tissues of the developing chick embryo.
纤维状胶原蛋白和非纤维状胶原蛋白构成了胶原蛋白家族中的两个主要类别,这两类胶原蛋白在各种各样的组织纤维中均有发现。IX型胶原蛋白属于非纤维状胶原蛋白类别;已鉴定出IX型胶原蛋白的三个不同亚基,其中α1和α2亚基已被克隆。我们使用分子克隆方法,从一个胚胎鸡软骨文库中分离出了编码鸡IX型胶原蛋白完整α3链的cDNA克隆。这些cDNA克隆包含2416个碱基对,其概念性开放阅读框编码一个含有675个氨基酸的蛋白质,其中包括193个Gly-X-Y重复序列。这些胶原蛋白重复序列分布在三个独立的结构域中,其间穿插着四个主要的非胶原蛋白结构域。胶原蛋白重复序列还有四处小的中断。这种链结构与鸡IX型胶原蛋白的α1和α2链直接对齐。将推导的氨基酸序列与IX型胶原蛋白的肽序列进行比较,结果显示与鸡α3链的96个已知残基中的95个以及牛α3链的98个已知残基中的81个相同。相同的残基与五个肽片段中的残基匹配,其中两个来自牛蛋白,三个来自鸡蛋白。鸡和牛的α3链具有保守的交联位点,它们被137个残基隔开,跨度为40纳米,即胶原纤维中空洞区的长度。鸡α3链的NC3结构域包含一个重复的半胱氨酸-脯氨酸基序,该基序在脊椎动物和无脊椎动物的非纤维状胶原蛋白中均存在。Northern印迹杂交显示有一条约3.3千碱基的主要mRNA;这种转录本在胚胎的软骨组织中被发现,包括发育中的肢体,而在其他组织或肢体发育的预凝聚阶段未检测到。综合数据描绘了鸡IX型胶原蛋白α3链的一级结构,显示了它与α1和α2链的密切关系,展示了其mRNA转录本,并表明该转录本在发育中的鸡胚胎组织中的出现情况。