Copeland Paul R
Department of Molecular Genetics, Microbiology and Immunology, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, 675 Hoes Ln Rm 728, Piscataway, NJ 08854, USA.
Gene. 2003 Jul 17;312:17-25. doi: 10.1016/s0378-1119(03)00588-2.
The regulation of gene expression at the translational level not only allows for rapid changes in specific protein levels but also provides an opportunity to alter codon specificity. For the incorporation of selenocysteine (Sec) into protein, the UGA codon is transformed from one that signals translation termination to one specific for Sec. This review provides a look at Sec incorporation from the perspective of the individual steps involved in protein synthesis: initiation, elongation and termination. The roles of the factors known to be required for Sec incorporation are considered in the context of each step in translation including structural modeling of the differences between the standard elongation factor eEF1A and the Sec-specific counterpart, eEFSec.
在翻译水平上对基因表达的调控不仅允许特定蛋白质水平的快速变化,还提供了改变密码子特异性的机会。为了将硒代半胱氨酸(Sec)掺入蛋白质中,UGA密码子从一个信号翻译终止的密码子转变为一个特定于Sec的密码子。本综述从蛋白质合成所涉及的各个步骤的角度审视Sec掺入:起始、延伸和终止。在翻译的每个步骤的背景下考虑已知Sec掺入所需的因子的作用,包括标准延伸因子eEF1A和Sec特异性对应物eEFSec之间差异的结构建模。