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Four groups of oligonucleotides were successively cloned in pMD18-T vector to obtain four large fragments. Ligation of these four fragments resulted in a cloned DNA MgE717 coding for the 29~268 amino acid region of gE. Sequencing result showed that there is a mutation at 255 amino acid, Asn instead of Asp.

分四段分别合成,基因拼接得到了改造后的基因片段MgE717,经测序,除了在gE基因+763位核苷酸处存在一碱基置换,导致第255位的氨基酸残基由Asp突变为Asn,其余的序列与PrV鄂A株gE基因的氨基酸序列相符。

The gene substitution model analysis showed thatsubstitution of B for C allele at αs1-Casein locus had a significant(p<0.05)effect on305-day milk yield,but not for milk fat percent;substitution of A1at β-Casein locus had ainfluence on 305-day milk yield,fat and protein percent;substitution of A at κ-Casein andβ-Lactoglobulin loci had no significant effect on all production performance.

基因替代模型的分析表明,αs1-CN位点B基因对C的替代显著影响305天产奶量,对乳脂率无显著影响,β-CN A1基因的替代对305天产奶量乳脂率和乳蛋率均有显著影响作用,κ-CN和β-LG位点A基因的替代对生产性能均无显著效应。

No fragments were amplified from some loci of EST-SSRs, which may suggest the loss of these loci in mirror carp genome or sequence divergence at the primer binding sites. These null alleles may result from selection because functional genes are under more selection pressure than non-encoding loci. Overall, population genetic variation is high for each of the five mirror carp, and the differentiations are also significant among populations.

3在与功能基因相关的多个微卫星基因座位上,扩增产物呈现不同程度的缺失现象,这些无效等位基因的产生可能与结构基因在育种中受到人工选择的影响较大有关。

An operator is a segment of DNA which regulates the activity of the structural genes of the operon that it is linked to, by interacting with a specific repressor or activator .

操纵基因是 DNA 的一节能调控与操纵子连结的结构基因的活动,这种调控是透过独特阻遏基因或活跃基因的相互作用。

Objective To detect the abnormal YRRM gene in azoospermia and to explore the pattern of YRRM gene in Chinese men.

目的 探索无精子症因子基因的候选基因之一YRRM基因在无精子症患者中的异常,了解中国人群的YRRM基因的形式。

Positive rate was relatively high, and the foreign gene could also maintain in testicular tissue for a long time, it could still be detected in the tissue in 7 months after being injected. However. Deferent results could be gained when the detection were made with different primers on different sites of the recombinant plasmid. This could be explained by transgene lost when the foreign gene recombinated and integrated in heterogenetic cell, or transgene degradated by cell nucleases.

然而,我们也看到,在后代检测中,利用不同的引物扩增重组质粒不同部位时,检测结果存在差异,转基因阳性率不同,这种差异说明当外源基因进入到异源细胞内,在重组整合时发生了外源基因丢失的现象,并由此导致外源基因的整合率下降,也可能是受细胞内核酸酶的作用,使得外源基因遭到降解。

To screen the sensitive and resistant yeast mutant when they treated with drug, the recombine technology of yeast gene should be applied to obtain the clone expressing the homeotic gene.

通过使用药物对特定的酵母基因突变株进行干预,筛选出对药物敏感或抵抗的突变株,然后利用酵母基因重组技术,使突变株再表达同源的基因,从而获得再表达同一基因的克隆。

According to molecular phylogenetic analysis of MADS1, MOC1, and TB1 alleles, the bamboo species may be divided to three main monophyletic group, but they are not corresponded to diffuse, unicaespitose and pluricaespitose bamboo.

进一步对不同基因(MADS1、MOC1和TB1)的系统进化作了比较,发现MOC1基因的系统进化分析结果对现有分类体系的支持最多,MADS1基因次之,而TB1基因可能不适用于竹类植物的系统进化与分类分析。

We sequenced the whole genome of the proband, identified all potential functional variants in genes likely to be related to the disease, and genotyped these variants in the affected family members.

我们对该病的先证者进行全基因测序,鉴定所有可能与该病相关的功能性变异基因,并确定在受累家族成员中这些变异基因的基因型。

Used the method of touch down PCR, the ACS2 gene was cloned from DNA of Petunia hybrida. At the same time, its gene sequence DQ090003 was obtained in GenBank, the antisense repetition of ACS2 linked the plasmid pBI-121 by use of one step. In the result, the expression vector having antisense repetition gene was constucted.

利用降落PCR的方法,从矮牵牛DNA中扩增出ACS2基因片段,在GenBank中获得基因序列号为DQ090003;利用一步法将ACS2基因的反义重复与pBI-121质粒连接,构建含该基因的反义重复表达载体。

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然而,正如其名字所指出的那样,CD盘不能写,也不能用任何方式改变其内容。

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