Cuif M H, Cognet M, Boquet D, Tremp G, Kahn A, Vaulont S
Laboratoire de Recherches en Génétique et Pathologie Moléculaires, Institut National de la Santé et de la Recherche Médicale Unité 129, Paris, France.
Mol Cell Biol. 1992 Nov;12(11):4852-61. doi: 10.1128/mcb.12.11.4852-4861.1992.
L-type pyruvate kinase (L-PK) is a key enzyme of the glycolytic pathway specifically expressed in the liver and, to a lesser degree, in the small intestine and kidney. One important characteristic of L-PK gene expression is its strong activation by glucose and insulin and its complete inhibition by fasting or glucagon treatment. Having previously established that the entire rat L-PK gene plus 3.2 kbp of 5'-flanking region functions in mice in a tissue-specific and hormonally regulated manner, various deletions of these 3.2 kbp of 5'-flanking regions were tested in transgenic animals to map the cis-acting elements involved in transcriptional gene regulation. Our experiments indicate that the proximal region between -183 and +11 confers tissue specificity and contains all the information necessary for dietary and hormonal control of L-PK gene expression in vivo. We found, however, that the transcriptional activity generated by this proximal promoter fragment can be modulated by distal sequences in a tissue-specific manner. (i) Sequences between bp -183 and -392 seem to play a dual role in the liver and small intestine; they induce L-PK expression in the liver but repress it in the small intestine. (ii) Sequences from bp -392 up to -1170 do not seem to have any additional effect on promoter activity. (iii) Between bp -1170 and -2080, we found a putative extinguisher whose transcriptional inhibitory effect is much more marked in the small intestine than in the liver. (iv) Finally, between bp -2080 and -3200, we identified an activating sequence required for full expression of the gene in the liver.
L型丙酮酸激酶(L-PK)是糖酵解途径中的关键酶,在肝脏中特异性表达,在小肠和肾脏中的表达程度较低。L-PK基因表达的一个重要特征是其受到葡萄糖和胰岛素的强烈激活,而禁食或胰高血糖素处理则可使其完全抑制。我们之前已经确定,完整的大鼠L-PK基因加上3.2kbp的5'侧翼区域在小鼠中以组织特异性和激素调节的方式发挥作用,因此在转基因动物中测试了这3.2kbp的5'侧翼区域的各种缺失情况,以定位参与转录基因调控的顺式作用元件。我们的实验表明,-183至+11之间的近端区域赋予组织特异性,并包含体内L-PK基因表达的饮食和激素控制所需的所有信息。然而,我们发现该近端启动子片段产生的转录活性可被远端序列以组织特异性方式调节。(i)-183至-392bp之间的序列在肝脏和小肠中似乎发挥双重作用;它们在肝脏中诱导L-PK表达,但在小肠中抑制其表达。(ii)-392至-1170bp的序列似乎对启动子活性没有任何额外影响。(iii)在-1170至-2080bp之间,我们发现了一个推定的抑制子,其转录抑制作用在小肠中比在肝脏中更为明显。(iv)最后,在-2080至-3200bp之间,我们鉴定出一个肝脏中基因完全表达所需的激活序列。