Garver F A, Chang L, Mendicino J, Isobe T, Osserman E F
Proc Natl Acad Sci U S A. 1975 Nov;72(11):4559-63. doi: 10.1073/pnas.72.11.4559.
An internal molecular deletion occurring in a human lambda type immunoglobulin light (L)-chain (Sm lambda) has been defined by sequence analysis. The Sm protein was isolated from the urine of a patient with a plasma cell dyscrasia involving the synthesis of an IgG molecule with both deleted gamma and lambda subunits. The Sm lambda polypeptide chain has an approximate molecular weight of 15,000 and contains 135 amino-acid residues. The constant (C) region is fully intact, comprising 105 residues, whereas the variable region (V) has only 30 residues. The V-region segment represents residues 1 through 30 of normal lambda chains and possesses considerable homology (87%) to lambda chains of subgroup II. Since lambdaII proteins normally contain 216 amino-acid residues, the defect represents an intramolecular deletion of 81 residues, which is entirely confined to the carboxyterminal three-quarters segment of the V-region, with a resumption of normal synthesis at a glutaminyl residue at position 110, the initiation point of the C-region. Carbohydrate is attached to an Asx residue at position 25, in the first hypervariable region, associated with the sequence triplet Asx-Ser-Ser, which is postulated to be a common recognition site for glycosylation of immunoglobulins. The carbohydrate moiety is a complex oligosaccharide with a branched chain structure containing sialic acid, fucose, mannose, N-acetylglucosamine, and galactose. These structural studies and other findings suggest that restricted areas in the DNA of immunoglobulin genes, such as the hinge regions of heavy (H) and light (L) chains and the hypervariable regions, are particularly susceptible to breakage and reunion. We postulate that the genetic defect of protein Sm could have originated from a somatic mutational event in the plasmacyte precursor during or after the integration of the V and C genes. These studies provide additional support for the hypothesis and two distinct structural genes encode a single immunoglobulin polypeptide chain.
通过序列分析确定了人类λ型免疫球蛋白轻链(Sm λ)中发生的一种内部分子缺失。Sm蛋白是从一名浆细胞发育异常患者的尿液中分离出来的,该患者合成的IgG分子同时具有缺失的γ和λ亚基。Sm λ多肽链的分子量约为15,000,包含135个氨基酸残基。恒定(C)区完全完整,由105个残基组成,而可变区(V)仅有30个残基。V区片段代表正常λ链的第1至30个残基,与II亚组的λ链具有相当高的同源性(87%)。由于λII蛋白通常含有216个氨基酸残基,该缺陷代表81个残基的分子内缺失,完全局限于V区的羧基末端四分之三片段,在第110位谷氨酰胺残基(C区的起始点)恢复正常合成。碳水化合物连接在第一个高变区第25位的Asx残基上,与序列三联体Asx - Ser - Ser相关,推测这是免疫球蛋白糖基化的一个常见识别位点。碳水化合物部分是一种具有分支链结构的复合寡糖,含有唾液酸、岩藻糖、甘露糖、N - 乙酰葡糖胺和半乳糖。这些结构研究和其他发现表明,免疫球蛋白基因DNA中的特定区域,如重链(H)和轻链(L)的铰链区以及高变区,特别容易发生断裂和重连。我们推测蛋白Sm的基因缺陷可能源于浆细胞前体在V基因和C基因整合期间或之后的体细胞突变事件。这些研究为单一免疫球蛋白多肽链由两个不同结构基因编码的假说提供了额外支持。