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可诱导的乳糖操纵子-阻遏物系统在非洲爪蟾卵母细胞中对注射DNA的表达控制起作用。

The inducible lac operator-repressor system is functional for control of expression of injected DNA in Xenopus oocytes.

作者信息

Hu M C, Davidson N

机构信息

Church Chemical Laboratories, California Institute of Technology, Pasadena 91125.

出版信息

Gene. 1988;62(2):301-13. doi: 10.1016/0378-1119(88)90567-7.

Abstract

We have investigated the use of the Escherichia coli lac operator-repressor system to regulate the expression of genes introduced by microinjection into Xenopus laevis oocytes. We observe that expression of an MSV-cat fusion gene, in which the lac operator was inserted between the TATA box and the transcription start point (tsp), or between the tsp and the start codon (ATG), is completely repressed when the lac repressor protein is added to the plasmid suspension prior to injection. The lac repressor had no detectable effect on the expression of a coinjected HSV-1 tk gene that had no operator insertion (or on an MSV-cat gene without an operator), indicating that the nonspecific DNA-binding properties of the repressor do not inhibit transcription. CAT activity expressed from the operator-containing MSV-cat genes transcribed in the oocyte nucleus was also inhibited by repressor injected into the oocyte cytoplasm, showing that biologically active repressor proteins can enter the nucleus from the cytoplasm. Injection of the inducer IPTG into the oocyte cytoplasm markedly derepressed the repressed cat genes but not the HSV-1 tk gene coinjected as an internal control. Overall, our results show that the lac operator-repressor system can be useful as a genetic switch in the regulation of gene expression of injected DNA in frog oocytes. Finally, our observations on the vectors used in this work show that the MSV enhancer significantly activates transcription from the SV40 early promoter in frog oocytes, although previous studies have indicated that the MSV enhancer is not necessary for the activity of the MSV promoter in oocytes [Graves et al., Mol. Cell. Biol. 5 (1985) 1945-1958].

摘要

我们研究了利用大肠杆菌乳糖操纵子 - 阻遏物系统来调控通过显微注射导入非洲爪蟾卵母细胞的基因的表达。我们观察到,对于一个MSV - cat融合基因,当在注射前将乳糖阻遏蛋白添加到质粒悬浮液中时,其表达会被完全抑制。该融合基因中,乳糖操纵子插入在TATA框和转录起始点(tsp)之间,或者在tsp和起始密码子(ATG)之间。乳糖阻遏物对共注射的没有操纵子插入的单纯疱疹病毒1型胸苷激酶(HSV - 1 tk)基因(或对没有操纵子的MSV - cat基因)的表达没有可检测到的影响,这表明阻遏物的非特异性DNA结合特性不会抑制转录。从在卵母细胞核中转录的含操纵子的MSV - cat基因表达的氯霉素乙酰转移酶(CAT)活性,也会被注射到卵母细胞细胞质中的阻遏物所抑制,这表明具有生物活性的阻遏蛋白可以从细胞质进入细胞核。向卵母细胞细胞质中注射诱导剂异丙基 - β - D - 硫代半乳糖苷(IPTG)能显著解除对被抑制的cat基因的抑制,但对作为内部对照共注射的HSV - 1 tk基因没有影响。总体而言,我们的结果表明,乳糖操纵子 - 阻遏物系统可作为一种基因开关,用于调控蛙卵母细胞中注射DNA的基因表达。最后,我们对本研究中所使用载体的观察表明,尽管先前的研究表明MSV增强子对于卵母细胞中MSV启动子的活性并非必需[格雷夫斯等人,《分子与细胞生物学》5(1985)1945 - 1958],但MSV增强子能显著激活蛙卵母细胞中SV40早期启动子的转录。

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