Ace Christopher I, Okulicz William C
Department of Physiology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
DNA Cell Biol. 2005 Jun;24(6):345-9. doi: 10.1089/dna.2005.24.345.
DMBT1 (deleted in malignant brain tumors) encodes a large scavenger receptor cysteine rich (SRCR) protein with proposed tumor suppressor properties due to its frequent deletion or lack of expression in a variety of different tumors including endometrial cancers. The gene is alternatively spliced to produce a number of related proteins with suspected functions in mucosal inflammation and epithelial regeneration. Expression of DMBT1 has been demonstrated in a wide variety of cell types, mostly of epithelial origin, including tissues of the respiratory system, the alimentary system, brain, and reproductive system. We have previously identified a Rhesus monkey cDNA clone H3 (homologous to human DMBT1) as a progesterone-induced gene in Rhesus monkey endometrium during the secretory phase of the menstrual cycle. As an initial step in understanding the molecular mechanisms of H3 (DMBT1) regulation we have cloned and sequenced 1.5 kb of the 5'-flanking region expected to contain promoter sequences of the Rhesus monkey gene and identified six putative progesterone receptor binding sites in the 5'-upstream region.
DMBT1(恶性脑肿瘤中缺失)编码一种富含半胱氨酸的大型清道夫受体(SRCR)蛋白,由于其在包括子宫内膜癌在内的多种不同肿瘤中频繁缺失或表达缺失,因而具有肿瘤抑制特性。该基因通过可变剪接产生多种相关蛋白,这些蛋白在黏膜炎症和上皮再生中可能具有一定功能。DMBT1已在多种细胞类型中得到证实,这些细胞大多起源于上皮细胞,包括呼吸系统、消化系统、脑和生殖系统的组织。我们之前已鉴定出恒河猴cDNA克隆H3(与人DMBT1同源)是月经周期分泌期恒河猴子宫内膜中的一种孕激素诱导基因。作为了解H3(DMBT1)调控分子机制的第一步,我们克隆并测序了预计包含恒河猴基因启动子序列的1.5 kb 5'侧翼区域,并在5'上游区域鉴定出六个假定的孕激素受体结合位点。