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The paper discussed how docosahexaenoic acid regulated transcription expression of lipogenic and lipolytic genes, which included PPARγ(peroxisome proliferators activated receptor γ), SREBP-1c (sterol regulatory element binding protein-1c), FAS, HSL (hormone-sensitive lipase) and TGH.

探讨二十二碳六烯酸对小鼠脂肪组织和肝脏生脂相关基因过氧化物酶增殖物激活受体γ、固醇调节元件结合蛋白－1c基因(SREBP-1c)、脂肪酸合成酶基因，及脂解相关基因激素敏感脂酶基因和甘油三酯水解酶时序表达的影响。

The bHLH transcription factor such as JAMYC2, JAMYC10, AtMYC2, BERJ1 and so on responsive to JAs were found in Arabidopsis thaliana, oryza sativa, Lycopersicon esculentum and many other plants, JAs can induce the expression of these genes.

在拟南芥、水稻和西红柿等植物中，发现了许多响应茉莉酸信号的bHLH家族转录因子基因，如JAMYC2、JAMYC10、AtMYC2和BERJ1等，茉莉酸可诱导这些基因的表达。

Permissive cells allow the transcription and translation of the transcriptional activator protein, which activates the early genes of the virus and the lytic cycle.

容纳性细胞允许转录活化蛋白的转录和翻译，其激活病毒的早期基因和溶解性周期。

CAAT box" and "TATA box, potential regulatory motifs from transcription, and conserved cis-acting regulator elements were discovered within LTRs in the great number of sequences using plantCARE sortware.6 The insertional polymorphism of LTR-10 element within the genome of 8 wild species and 28 cultivars of Mallus Mill. was studied by sequence-specific amplification polymorphism.

分析获得的Tyl-copia类逆转座子的LTRs，其中含有启动子的结构特征&CAAT box&和&TATA box&及受不同胁迫条件作用的调控元件。6、基于苹果Tyl-copia类逆转座子LTR-10的SSAP技术在苹果属8个野生种和28个栽培品种中表现出了丰富的遗传多态性，多态性片段比例为88.2％。

In R.trifolii, matABC operon participates in malonate metabolism, and regulated by GntR transcription regulator MatR.

在三叶草根瘤菌中， matABC操纵子参与丙二酸的代谢，受到GntR转录调控因子MatR调控。

With the method of reverse transcription-polymerase chain reaction and nest PCR, P80 gene of CSFV is cloned from the cells infected by the strain Shimen of csfv, and connected with eukaryotic expression vector pEGFP-C1. Then recombined eukaryotic expression plasmid pEGFP-P80 of P80 gene is achieved successfully. It builds the basis for expressing and gaining protein p80 in mammiferous cells.

利用反转录PCR和套式PCR技术，从猪瘟病毒Shimen株细胞毒中克隆出P80 基因，并进一步把P80 基因连接在真核表达载体pEGFP-C1 上，成功地构建出P80 基因重组真核表达质粒(pEGFP-P80)，为在哺乳动物细胞中表达并纯化出p80 蛋白奠定了基础。

This study is using of yeast one-hybrid system to identify the transcription factor function of Medicago truncatula DREB1A gene, for which the basis to the study of gene cold-resistant functions.

本研究就是利用酵母单杂交系统鉴定蒺藜苜蓿DREB1A基因的转录因子功能，为该基因的耐寒功能研究奠定基础。

The transcription initiation start site of a predicted honeybee MLC-2 gene (myosin regulatory light chain 2) was localized on the genome sequence of Apis mellifera with the head of drone's 5'Long-SAGE tags mapping to genome sequences in this study, and the structure of promoter was predicted.

使用西方蜜蜂雄蜂头部5'LongSAGE文库中的肌球蛋白调节性轻链基因MLC-2的标签序列，在蜜蜂全基因组序列上定位了该基因的转录起始位点，并进而预测了其启动子的结构。

Micrococcal lysis assay of the milk samples showed that the cDNA was efficiently expressed in the mammary glands with similar expression levels ranging from 60 to 87 mg/L. Different tissues of each vector-injected mouse were assayed for transcription of hLYZ mRNA by dot-blotting and for expression of hLYZ activity by Micrococcal lysis assay. The results showed that expression of the three recombinant vectors was mainly restricted to mammary glands with some degrees of ectopic expression in spleen, intestines and/or kidney.

注射后72 h采集乳样，经微球菌溶解实验证明，3组小鼠乳汁中hLYZ的表达量分别为87、69、60 mg/L；从每组小鼠的12种组织提取总RNA，经Dot blotting检测证明，三种重组载体除在乳腺中表达外，p205C3LYZ还在小鼠的脾和肠、pBJLYZ在脾、pBCLYZ在脾和肾中具有一定的异位表达；在有hLYZ mRNA转录的上述脏器中用微球菌溶解试验均可检测到hLYZ活性。

The mRNA expression of tyrosinase and microphthalmia transcription factor was examined with semiquantitative RT-PCR.

并可以促进酪氨酸酶和 MITF的基因表达。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。