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Cloning, sequencing, and expression analysis of the porcine uroplakin II gene.

作者信息

Kwon Deug-Na m, Seo Han Geuk, Kim Jin-Hoi

机构信息

Division of Applied Life Science, College of Agriculture, Gyeongsang National University, Chinju, GyeongNam 660-701, Republic of Korea [corrected].

出版信息

Biochem Biophys Res Commun. 2002 May 3;293(2):862-9. doi: 10.1016/S0006-291X(02)00295-4.

Abstract

In this study, we report the cloning of porcine UPII genomic DNA, which contains a putative full-length open reading frame encoding the UPII protein. A comparison of the porcine UPII gene coding sequence with the previously published mouse UPII sequence demonstrates that the exon sequences are only partially conserved. Northern and immunohistochemical analyses show that the porcine UPII gene is expressed only in the urothelium and that the protein specifically localizes to urothelial superficial cells. Among urothelial superficial cells, 8.5-9.8% of umbrella cells expresses the UPII gene. A 2-kb region of the porcine UPII promoter contains multiple transcription factor binding sites, including GC-boxes, SP1, AP2, and GATA-box sites, but no TATA or CAAT-box sequences. A sequence comparison of the porcine and murine UPII promoter genes by the MEME system allowed two conserved motifs to be identified, suggesting that these sequences have cis-acting regulatory roles. Sequence homologies between the motifs A and B of the two species are 79% and 80%, respectively, although their relative locations are different. Our results show that the porcine UPII gene is expressed highly and specifically in the bladder urothelium.

摘要

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