Bachwich D, Merchant J, Brand S J
Gastrointestinal Unit, Massachusetts General Hospital, Boston 02114.
Mol Endocrinol. 1992 Aug;6(8):1175-84. doi: 10.1210/mend.6.8.1357547.
Antral gastrin secretion and gene expression is inhibited by the paracrine release of somatostatin from antral D cells. Transforming growth factor-alpha and epidermal growth factor (EGF) stimulate gastrin reporter gene constructs when transfected into pituitary GH4 cells. Somatostatin inhibits EGF stimulation of gastrin gene expression, which is in part mediated at the level of transcriptional regulation as somatostatin inhibits EGF stimulation of gastrin reporter gene constructs. Somatostatin inhibition was abolished by pertussis toxin, indicating somatostatin inhibits transcription through the inhibitory G protein Gi. Somatostatin inhibition was unaffected by vanadate and okadaic acid, implying this inhibitory pathway is mediated neither through phosphotyrosine phosphatases nor serine/threonine phosphatases, respectively. Gastrin reporter genes containing 82 base pairs of the 5'-flanking DNA were sufficient to confer both EGF responsiveness and inhibition by somatostatin in GH4 cells. However, transcription of a gastrin reporter gene construct containing only the EGF response element (GGGGCGGGGTGGGGGG), located at -68 to -53, was stimulated by EGF but was not inhibited by somatostatin. Thus, somatostatin inhibits EGF-stimulated gastrin gene transcription by a mechanism other than by interfering with cell signals elicited by the EGF receptor. Since the 82 GASCAT is inhibited by somatostatin, this result also implies that sequences adjacent to the EGF response element contain a cis-regulatory element mediating transcriptional inhibition by somatostatin. This cis-element was located using gastrin reporter genes comprising sequential segments of the human gastrin promoter sequence from the transcriptional start site to -82 in the 5'-flanking DNA. Gastrin oligonucleotide constructs lacking the D oligonucleotide (gatcCATATGGCAGGGTA), located at -82 to -69 in the 5'-flanking DNA, were not inhibited by somatostatin, indicating that a somatostatin inhibitory cis-element is located between -82 and -69 in the 5'-flanking DNA of the human gastrin promoter.
胃窦部D细胞旁分泌释放的生长抑素可抑制胃窦部胃泌素的分泌及基因表达。将转化生长因子-α和表皮生长因子(EGF)转染至垂体GH4细胞时,可刺激胃泌素报告基因构建体。生长抑素抑制EGF对胃泌素基因表达的刺激作用,这部分是在转录调控水平介导的,因为生长抑素抑制EGF对胃泌素报告基因构建体的刺激。百日咳毒素可消除生长抑素的抑制作用,表明生长抑素通过抑制性G蛋白Gi抑制转录。生长抑素的抑制作用不受钒酸盐和冈田酸的影响,这意味着该抑制途径分别不是通过磷酸酪氨酸磷酸酶和丝氨酸/苏氨酸磷酸酶介导的。含有82个碱基对5'-侧翼DNA的胃泌素报告基因足以赋予GH4细胞中EGF反应性和生长抑素抑制作用。然而,仅含有位于-68至-53的EGF反应元件(GGGGCGGGGTGGGGGG)的胃泌素报告基因构建体的转录受到EGF刺激,但不受生长抑素抑制。因此,生长抑素通过不同于干扰EGF受体引发的细胞信号的机制抑制EGF刺激的胃泌素基因转录。由于82个GASCAT受到生长抑素的抑制,该结果还意味着与EGF反应元件相邻的序列包含介导生长抑素转录抑制的顺式调节元件。使用包含从转录起始位点到5'-侧翼DNA中-82的人胃泌素启动子序列连续片段的胃泌素报告基因定位该顺式元件。缺乏位于5'-侧翼DNA中-82至-69的D寡核苷酸(gatcCATATGGCAGGGTA)的胃泌素寡核苷酸构建体不受生长抑素抑制,表明生长抑素抑制性顺式元件位于人胃泌素启动子5'-侧翼DNA的-82至-69之间。