Cobaleda C, Sánchez-García I
Instituto de Biología Molecular y Celular del Cáncer, Centro de Investigación del Cáncer, CSIC/Universidad de Salamanca, Campus Unamuno, 37007-Salamanca, Spain.
Trends Biotechnol. 2001 Oct;19(10):406-11. doi: 10.1016/S0167-7799(01)01741-3.
The M1 RNA subunit of Escherichia coli RNase P is a ribozyme responsible for the catalytic activity of the complex. It removes the 5' leader sequence from tRNA precursors to form mature tRNAs. M1 recognizes its target mainly on the basis of its structure and this allows the design of modified ribozymes engineered to destroy other molecules without the need for special sequences in the targeted mRNAs. M1 is thus an ideal tool to eliminate the tumourigenic chimeric messengers created after chromosomal translocations. These results have direct implications for cancer therapeutics and molecular biology in general.
大肠杆菌核糖核酸酶P的M1 RNA亚基是一种核酶,负责该复合物的催化活性。它从tRNA前体中去除5'前导序列以形成成熟的tRNA。M1主要根据其结构识别其靶标,这使得能够设计出经过改造的核酶,用于破坏其他分子,而无需靶标mRNA中的特殊序列。因此,M1是消除染色体易位后产生的致癌嵌合信使的理想工具。这些结果对癌症治疗和一般分子生物学具有直接影响。