基因的

SQUA genes of Dendrocalamus latiflorus were sequenced, and phylogenetic form on SQUA genes in angiosperms was analyzed. Relative rate and adaptive evolution after SQUA gene duplication in recent common ancestor of monocots and eudicots were analyzed using the methods of relative rate test, statistic on synonymous and non-synonymous coden substitution sites and likelihood rate test.

测定了麻竹的SQUA基因序列并分析了被子植物中SOUA类基因的系统发育式样；采用相对速率检验、同义与非同义置换位点统计以及似然比检验方法，分析了单子叶和真双子叶植物最近共同祖先中SQUA基因发生基因重复后的进化速率与适应机制。

In this research work, the technology of microbial conversion was studied in order to establish an environment friendly method for the production of doxorubicin. A doxA gene encoding Daunorubicin C-14 hydroxylase was cloned from a daunorubicin-producing strain Streptomyces coeruleorubidus SIPI 1482. Some plasmids for the expression of doxA gene were constructed and transformed into S.

本研究对微生物转化法替代现有工艺生产阿霉素进行了探索，从柔红霉素产生菌天蓝淡红链霉菌SIPI 1482中克隆了柔红霉素C-14羟化酶基因，构建了doxA基因的链霉菌表达质粒，导入变铅青链霉菌TK24中获得了柔红霉素转化基因工程菌，并研究了doxA基因在工程菌中的表达，最后还对工程菌转化柔红霉素生成阿霉素的发酵工艺进行了初步研究。

The invention clones geranyl pyrophosphate synthase GGPPS gene from the ginkgo to construct plant expression vectors which contain ggpps gene, the ggpps gene is inducted into immature embryos of the ginkgo to induct out the callus tissue by the mediating of agrobacterium tumefaciens, PCR and semiquantitative RT-PCR detect the conformation and expression status of exogenous target gene ggpps, high-performance liquid chromatography and an evaporative light-scattering detector are employed to determine the terpene lactones content inside the callus tissue of the ginkgo, and the obtained callus tissue of the ginkgo of which the terpene lactones content is increased is screened.

本发明从银杏中克隆香叶基香叶基焦磷酸合成酶GGPPS基因，构建含ggpps基因的植物表达载体，用根癌农杆菌介导，将ggpps基因导入银杏幼胚并诱导出愈伤组织，PCR和半定量RT-PCR检测外源目的基因ggpps的整合和表达情况，高效液相色谱法及蒸发光散射检测器测定银杏愈伤组织中萜内酯含量，筛选获得银杏萜内酯含量提高的转基因银杏愈伤组织。

Assisted by DNA2.0 and Gene2Oliga software, we optimized the codon usage and secondary structure of RNA and induced enzyme sites Cla I (237 site) and Pst I (475 site) into the gene. In the first step, fragments F1 (237 bp), F2 (238 bp) and F3 (422 bp) were separately synthesized by assembly PCR. In the second step, fragments F1, F2 and F3 were separately digested by Cla I and Pst I, and then ligated into a full length lipA gene.

首先在DNA2.0和Gene2Oliga软件辅助下对lipA基因密码子及RNA二级结构进行优化并引入Cla I(237位)和Pst I(475位)酶切位点；通过组装PCR分别合成lipA基因的各片段F1(237 bp)、F2(238 bp)和F3(422 bp)；通过该基因内的Cla I和Pst I限制性酶切位点连接成完整的全长lipA基因。

Then we transformed mTn-lacZ/LEU2 transposon library into the YES2MTM1 strain. Transformants lost the plasmid overexpressing MTM1 after 5-Fluoroorotic acid treatment. We picked up the yeast strains able to grow on nonfermentable carbon source with MTM1 deletion and some transposon insertion and identified the insertion sites.

因MTM1基因的缺失造成的损伤不可逆，直接转入文库无法筛选得到MTM1 基因缺失表型相关基因，本研究利用外源MTM1基因菌株和mTn-lacZ/LEU2酿酒酵母转座子文库进行筛选，寻找能挽救mtm1突变体生长缺陷的转座子插入位点。

Opportunistically expressed (usually at the basal levels of transcription), but still permit the continued expression of genes that are regulated by strong promoters/enhancers (such as housing-keeping gene), the expresison of these genes might play a key role in the embryonic development; 5 The sum of these two opposing processes-activation and repression-would dictate the final pattern of gene expression that manifests itself as a dramatic reprogramming of gene expression during the maternal-to-zygotic transition and support further embryonic development.

这些基因的表达对于胚胎的后继发育可能是至关重要的；5）通过胚胎基因表达的激活与抑制：这两个作用相反的机制依不同时间顺序协同作用于胚胎基因，从而在指导胚胎发育的控制权由母源性表达产物移交到胚胎特异的基因表达产物的过程中&再程序化&胚胎基因的表达，形成特定的表达模式，以支持胚胎的后继发育。

Regulator gene A gene whose product can promotor or prevent the TRANSCRIPTION of structural genes, which may or may not be adjacent to other regulator genes, and may even be on another chromosome.

调节基因：这种基因的产物可以促进或抑制结构基因的转录，其可能与其他的调节基因相连，也可以不相连，甚至两者可以不在同一染色体上。

Therefore, we selected the 5 genes, as well as SMTN gene related to human cardiovascular diseases, for chromosomal mapping, CDS cloning and analysis, spatio-temporal distribution, mutation riddling, and association analysis with production traits of 3 porcine populations. We expect to know the structure and function of these 6 genes primarily, and supply data for porcine marker assistant selection of improving meat production.

因此，本研究选择NADH呼吸链相关基因，以及与人类心血管疾病相关的SMTN基因，以猪的骨骼肌为研究对象，用人×仓鼠体细胞杂种克隆板进行6个基因的染色体定位、CDS克隆和序列分析、用半定量RT-PCR进行时空表达谱分析、进行突变位点的筛选、并利用3个猪群的产肉性状资料进行基因型与性状的关联分析，以期初步了解这些基因的结构和功能，并为改进猪产肉性能的标记辅助选择提供资料。

In this study, based on establishment of stable and high efficient transfergenic receptor system with supersweet maize callus, the multiple insect-resistant genes were successfully co-transformed into a elite inbred line 1132 and a variety using particle bombardment and overy microinjection, and the transgenic integration, expression and inheritance were studied by means of target character and molecular biology method.

本研究在建立高效稳定基因转化受体系统的基础上，利用基因枪和子房注射两种方法将多个抗虫基因成功转化抗性较差的超甜玉米自交系及其品种，并从分子水平和目标性状上研究外源基因的转入、整合、表达与遗传规律。

All the normal cervical epithelial samples (10/10) and 90%(36/40) of cervicalcarcinomas had the positive lanes by using the unmethylated

然而，12例无基因甲基化的癌标本也有FHIT蛋白的异常表达，提示基因甲基化可以导致基因的失活，但不是基因失

However, as the name（read－only memory）implies, CD disks cannot be written onorchanged in any way.

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。

Galvanizes steel pallet is mainly export which suits standard packing of European Union, the North America. galvanizes steel pallet is suitable to heavy rack. Pallet surface can design plate type, corrugated and the gap form, satisfies the different requirements.

镀锌钢托盘多用于出口，替代木托盘，免薰蒸，符合欧盟、北美各国对出口货物包装材料的法令要求；喷涂钢托盘适用于重载上货架之用，托盘表面根据需要制作成平板状、波纹状及间隔形式，满足不同的使用要求。