stop codon

Sequence analysis revealed that abnormally processed transcripts resulted in frame-shifts with premature termination by introducing stop codon, removal of translation initiation codon and deletion of functional domain.

经序列分析，CMO基因转录本的异常加工将导致移码后提前终止及翻译起始密码或功能结构域的丢失。

As a stop codon reaches the A-site of a translating ribosome , either termination or readthrough occurs.

当终止密码子进入核糖体翻译的A位时,将会发生翻译终止或是通读.

All of them have been characterized to represent DNA alterations by sequencing, including 8 point mutations ( 6 missence, 1 silent mutation and 1 in intron) and a 1 base pair insertion ( introducing a stop codon downstream).

包括8个点突变（6个错义突变，1个静息突变和1个内含子突变）和1个碱基对插入突变（在下游产生终止信号）。

Mechanism of stop codon recognition of class I polypeptide release factor or termination codon reassignment are problems that have not yet been fully clarified, and should be further in-depth discussed.

总之，第一类肽链释放因子识别终止密码子的机制和终止密码子的重新分配机制是一个尚未完全瀍明的问题，有待做进一步深入的探讨。

Analyzed functional sites contain transcription start sites, transcriptional termination sites, start codon, stop codon and junction sites of intron and exon.

分析的功能位点包括：转录起始位点，转录终止位点，起始密码子，终止密码子，内含子和外显子连接处等。

Comparison of relative preference of nucleosome binding motifs shows that the mode number of preferred nucleosome motifs in ± 500bp region around the transcription start sites, transcription termination sites, start codon and stop codon is different.

但对核小体结合模体的相对偏好性进行比较后发现，转录起始位点、转录终止位点、起始密码子和终止密码子附近±500bp的序列所包含的偏好的核小体结合模体模式数各不相同。

However, stop codon susceptibility to gentamicin between different genes is difficult to predict.

但是, 不同基因的终止密码子对庆大霉素的易感性是难以预测的.