Degelmann A, Royer H D, Hollenberg C P
Chromosoma. 1979 Mar 12;71(3):263-81. doi: 10.1007/BF00287136.
Southern gel analysis of total DNA from Chironomus tentans showed that the rRNA genes (rDNA) are homogeneous in structure. After cloning in Escherichia coli plasmid pBR313, the rDNA organisation was further studied by restriction fragment analysis and R-loop mapping. No heterogeneity could be detected by heteroduplex analysis of six different cloned rRNA cistrons. R-loop sizes of 1.69 and 3.63 kilobases (kb) were measured for the 18S and 28S rRNA coding sequences. The two spacers are 0.75 and 1.77 kb long. Southern gel analysis showed also a homogeneous rDNA structure for a Canadian population of C. tentans and C. pallidivittatus. The same technique indicated, however, that the rDNA of two other closely related species of C. thummi and C. melanotus is heterogeneous in structure. A possible correlation between this heterogeneity and the presence of heterochromatin in these species is discussed.
对摇蚊的总DNA进行的Southern凝胶分析表明,核糖体RNA基因(rDNA)在结构上是同质的。在大肠杆菌质粒pBR313中克隆后,通过限制性片段分析和R环作图对rDNA组织进行了进一步研究。对六个不同克隆的rRNA顺反子进行异源双链分析未检测到异质性。测得18S和28S rRNA编码序列的R环大小分别为1.69和3.63千碱基(kb)。两个间隔区长度分别为0.75和1.77 kb。Southern凝胶分析还表明,加拿大的摇蚊和苍白摇蚊种群的rDNA结构是同质的。然而,相同技术表明,另外两种亲缘关系密切的摇蚊和黑摇蚊的rDNA在结构上是异质的。本文讨论了这种异质性与这些物种中异染色质存在之间的可能相关性。