Kuechler E, Rich A
Proc Natl Acad Sci U S A. 1969 Jun;63(2):520-7. doi: 10.1073/pnas.63.2.520.
Popliteal lymph nodes of rabbits stimulated to produce antibodies were pulse labeled in vivo by direct injection of (3)H-uridine. RNA was then extracted from isolated polysomes and single ribosomes. Fractionation of this RNA by polyacrylamide gel electrophoresis revealed the synthesis of two discrete peaks of labeled RNA migrating in the region between 18S ribosomal and 4S transfer RNA. These peaks were found in the RNA extracted from polysomes but were absent from single ribosomes. When the polysomes were disrupted by EDTA treatment the RNA species no longer appeared as rapidly sedimenting material. These two RNA's have molecular weights near 2.2 x 10(5) and 3.7 x 10(5) daltons. The chemical and biological properties of these species as well as the molecular weights are consistent with those expected for monocistronic messenger RNA coding for the antibody L and H chains, respectively.
通过直接注射(3)H - 尿苷在体内对受刺激产生抗体的兔腘淋巴结进行脉冲标记。然后从分离的多核糖体和单个核糖体中提取RNA。通过聚丙烯酰胺凝胶电泳对该RNA进行分级分离,结果显示合成了两个离散的标记RNA峰,它们在18S核糖体RNA和4S转移RNA之间的区域迁移。这些峰出现在从多核糖体提取的RNA中,而在单个核糖体中不存在。当用EDTA处理使多核糖体破坏时,这些RNA种类不再表现为快速沉降的物质。这两种RNA的分子量接近2.2×10(5)和3.7×10(5)道尔顿。这些种类的化学和生物学特性以及分子量与分别编码抗体L链和H链的单顺反子信使RNA所预期的特性一致。