splice site meaning in Chinese
剪接位点
Examples
- Grouped weight matrix for splice site recognition
模型的参数估计 - In this paper , grouped weight matrix ( gwm ) method is proposed for splice site recognition
摘要提出识别剪切位点的分组权重矩阵方法。 - One of these splicing signals sits at the beginning of the intron and is called the 5 ' ( five - prime ) splice site ; the others , located at the end of the intron , are known as the branch site , the polypyrimidine tract and , finally , the 3 ' ( three - prime ) splice site
其中一段位在插入子的起头，有一个剪接信号序列，标明5 '端剪接位；插入子的尾端有其他的信号：分支点、多嘧啶区，最后则是3 '端剪接位。 - A new method for the splicing - site recognition of rice dna sequences was designed . based on the gt - ag intron organization principal , support vector machines ( svm ) was used to predict the splicing sites . through machine learning , a model was built on some test data set of true and pseudo splicing sites
根据真核生物内含子在剪切位点前后存在保守碱基的特征，用支持向量机技术构建分类器模型，有效地在基因组序列中识别剪接位点， 3位点识别的准确度87 . 96 ，在5位点识别的准确度达85 . 41 。 - The mechanism is that the introduced complementary oligonucleotides can bind to the corresponding mrna or double - stranded dna in genome and form partial double - stranded molecules or triple - stranded nucleic acid molecules by sequence - specific and nonsequence - specific antisense action , thus the target gene will be orientationally blocked and expression of the target inhibited so that therapeutic effect could be attained . in this study , we designed a fragment of human c ii ta cdna in antisense orientation using mrna of c ii ta as template . the primers were designed based on 94 - 500 nucleotides segment in 5 " end of ciita gene so that the interested gene contained 407 base pairs which included two aug codons in 1 16 and 188 nucleotides as well as the splicing site between the first and the second exons
本研究设计以c tamrna为模板的反义cdna片段，从c ta基因5 ’端第94位到500位核苷酸段设计引物，目的片段407bp ，覆盖第116和188位两个aug密码子，也包含了第一外显子和第二外显子间的剪接位点：用常规分子生物学方法构建了反义片段的腺病毒表达载体( padeasy - 1系统) ；腺病毒载体经hek293细胞包装产生含反义片段的重组腺病毒，用氯化铯密度梯度离心法获得纯化的高滴度腺病毒；进行体外基因转移，分别用反义片段真核表达载体转染p388d1细胞和用重组腺病毒感染hela细胞，观察导入的c ta基因反义rna抑制细胞内组成型或诱导型c ta基因表达的作用，从而达到调控mhc -类分子表达的目的。