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关于一个控制小鼠λ1轻链表达的调控基因。

On a regulatory gene controlling the expression of the murine lambda1 light chain.

作者信息

Geckeler W, Faversham J, Cohn M

出版信息

J Exp Med. 1978 Nov 1;148(5):1122-36. doi: 10.1084/jem.148.5.1122.

Abstract

We describe here two alleles, an allele of the lambda1 locus present in the SJL strain (rlambda1lo) and an allele of the lambda1 locus present in the BALB/c strain (rlambda1 +), of a regulatory gene locus which specifically influences the expression of the mouse lambda1 light chain structural gene. The rlambda1 regulatory gene is not linked to either the major histocompatibility complex or to the heavy-chain allogroup but appears to be linked to the lambda1 structural gene locus. In the homozygous state, the present of the rlambda1lo allele results in a 50-fold reduction in the number of lambda1 antigen-sensitive, bone-marrow derived lymphocytes (ASCs) compared to the presence of the rlambda1 + allele. However, those few lambda1ASCs present in rlambda1lo homozygotes can be induced normally to produce lambda1 light chains indistinguishable from those found in rlambda1 + homozygotes. The reduction in lambda1ASC's due to the rlambda1lo allele results both in a reduction in the amount of lambda1 Ig in the serum and also in a large variation in the magnitude of the lambda1 antibody response to alpha(1,3) dextran by individual animals. This variation permits the estimate that, on the average, 50 B cells of anti-alpha(1,3) specificity must be present per animal to permit a measurable response. Surprisingly, the expression of a gene locus regulating lambda1 light chain expression (rlambda1 locus) shows a clear gene dosage effect with rlambda1lo/rlambda1 + heterozygotes having 1/2 the number of lambda1ASCs and 1/2 the amount of serum lambda1 Ig as rlambda1 +/rlambda1 + homozygotes. This fact permits an analysis of the relationship between germ-line v-genes and their individual expression in serum Ig. The rlambda1 locus controls specifically a DNA-level event which occurs in stem cells as they become committed to lambda1 light chain expression. We postulate that the rlambda1 locus represents one of the DNA level recognition sites involved in the translocation event which places the vlambda1 and clambda1 structural genes in a transcriptional unit.

摘要

我们在此描述了一个调控基因座的两个等位基因,一个是存在于SJL品系中的λ1基因座的等位基因(rlambda1lo),另一个是存在于BALB/c品系中的λ1基因座的等位基因(rlambda1 +),该调控基因座特异性地影响小鼠λ1轻链结构基因的表达。rlambda1调控基因既不与主要组织相容性复合体相连,也不与重链同种异型群相连,但似乎与λ1结构基因座相连。在纯合状态下,与rlambda1 +等位基因相比,rlambda1lo等位基因的存在导致λ1抗原敏感的骨髓来源淋巴细胞(ASC)数量减少50倍。然而,rlambda1lo纯合子中存在的少数λ1 ASC能够正常被诱导产生与rlambda1 +纯合子中发现的λ1轻链无法区分的λ1轻链。由于rlambda1lo等位基因导致的λ1 ASC数量减少,既导致血清中λ1 Ig量的减少,也导致个体动物对α(1,3)葡聚糖的λ1抗体反应强度的巨大差异。这种差异使得可以估计,平均而言,每只动物必须存在50个具有抗α(1,3)特异性的B细胞才能产生可测量的反应。令人惊讶的是,调控λ1轻链表达的基因座(rlambda1基因座)的表达显示出明显的基因剂量效应,rlambda1lo/rlambda1 +杂合子的λ1 ASC数量和血清λ1 Ig量是rlambda1 +/rlambda1 +纯合子的1/2。这一事实允许分析种系v基因与其在血清Ig中的个体表达之间 的关系。rlambda1基因座特异性地控制干细胞在开始表达λ1轻链时发生的DNA水平事件。我们推测,rlambda1基因座代表了参与将vlambda1和clambda1结构基因置于转录单位中的易位事件的DNA水平识别位点之一。

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