Biesbrock A R, Bobek L A, Levine M J
Department of Oral Biology and Research Center in Oral Biology, School of Dental Medicine, State University of New York at Buffalo, 14214, USA.
Glycoconj J. 1997 Jun;14(4):415-22. doi: 10.1023/a:1018587031814.
This study examined differential expression of several mucin genes in the human submandibular gland and trachea, MUC7 tissue and species specificity, and MUC7 genetic polymorphism. Mucin gene expression examined by RT-PCR indicated that MUC1, MUC4 and MUC7 are expressed in the human submandibular gland, while MUC1, MUC2, MUC4, MUC5 and MUC7 are expressed in the human trachea. Northern blot analysis confirmed the expression of MUC7 in the human trachea and MUC4 in the human submandibular gland. Northern blot analysis also demonstrated that MUC7 is not expressed in the submandibular/sublingual gland complexes of hamster, mouse and rat. Southern blot analysis suggested the presence of a MUC7 homologue in monkey genomic DNA. Genetic polymorphism studies of MUC7 by PCR and Southern blot analysis revealed the presence of a limited variable number of tandem repeats (VNTR) polymorphism.
本研究检测了几种黏蛋白基因在人类下颌下腺和气管中的差异表达、MUC7的组织和物种特异性以及MUC7基因多态性。通过逆转录聚合酶链反应(RT-PCR)检测黏蛋白基因表达表明,MUC1、MUC4和MUC7在人类下颌下腺中表达,而MUC1、MUC2、MUC4、MUC5和MUC7在人类气管中表达。Northern印迹分析证实了MUC7在人类气管中的表达以及MUC4在人类下颌下腺中的表达。Northern印迹分析还表明,MUC7在仓鼠、小鼠和大鼠的下颌下/舌下腺复合体中不表达。Southern印迹分析提示在猴基因组DNA中存在MUC7同源物。通过聚合酶链反应(PCR)和Southern印迹分析对MUC7进行的基因多态性研究揭示了有限数量的可变串联重复序列(VNTR)多态性的存在。