Genomic structure, organization and promoter analysis of the human F11R/F11 receptor/junctional adhesion molecule-1/JAM-A

• Published in: Gene 2006-01, Vol.366 (1), p.128-144
• Main Authors: Sobocki, T., Sobocka, M.B., Babinska, A., Ehrlich, Y.H., Banerjee, P., Kornecki, E.
• Format: Article
• Language: English
• Subjects: 5' Untranslated Regions - genetics; Blood Platelets - cytology; Blood Platelets - metabolism; CD321; Cell adhesion molecule; Cell Adhesion Molecules - biosynthesis; Cell Adhesion Molecules - genetics; Cell Adhesion Molecules - metabolism; Codon, Initiator - genetics; DNA, Complementary - genetics; Endothelial Cells - cytology; Endothelial Cells - metabolism; Endothelium; Exons - genetics; F11 receptor; F11R; HeLa Cells; Humans; Immunoglobulin superfamily; Inflammation - genetics; Inflammation - metabolism; JAM; JAM-A; K562 Cells; Organ Specificity - genetics; Platelet Aggregation - genetics; Platelets; Receptors, Cell Surface - biosynthesis; Receptors, Cell Surface - genetics; Receptors, Cell Surface - metabolism; Response Elements - genetics; RNA, Messenger - genetics; TATA Box - genetics; Thrombosis - genetics; Thrombosis - metabolism; Transcription, Genetic - genetics
• ISSN: 0378-1119; 1879-0038
• DOI: 10.1016/j.gene.2005.08.025

The F11-receptor (F11R) (a.k.a. JAM-1, JAM-A, CD321) is a cell adhesion molecule of the immunoglobulin superfamily involved in platelet adhesion, secretion and aggregation. In addition, the F11R plays a critical role in the function of endothelial cells and in platelet adhesion to inflamed endothelium. In the present study, we used partial sequences of the human F11R gene, F11R cDNAs, and information in unannotated human genome databases, to delineate the F11R gene. We found that the F11R gene is composed of 13 exons (E1a, 1b, 1c, E1–E10) encoding two groups of mRNAs differing in length and sequence at their 5′ UTRs, referred to as type 1 and type 2 messages. Type 1 cDNAs are shorter at the 5′ end and contain a region not found within type 2 messages. Type 1 mRNAs are present in endothelial cells (EC), platelets, white blood cells and in the cell lines CMK, HeLa, K562, HOG and A549, while type 2 messages are limited to EC. Type 1 messages contain exons E1–E10 whereas type 2 messages usually contain exons E1a, 1c, part of E1 and E2–E10. The translation start site is localized in the 3′ end of E1, common for both type 1 and type 2 messages. Expression of these messages is regulated by two alternative promoters, P1 and P2. P1 is a TATA-less promoter containing an initiator element, multiple transcription start sites, several GC and CCAAT boxes, and GATA, NF-κB and ets consensus sequences. The cloned P1 drives efficient expression of the luciferase reporter gene. A high level of similarity between human P1 and its rat and mouse counterparts was observed. Promoter P2, located upstream of P1, contains a TATA box, GC boxes, a CCAAT box and GATA and ets consensus sequences. 3′ RACE provided evidence for variability in the 3′ UTR due to the presence of two polyadenylation signals. The finding of multiple regulatory sites in the promoters supplements the biochemical evidence that the F11R has several different roles in the functional repertoire of endothelial cells, platelets and other cells. In particular, the presence of NF-κB provides additional evidence to the significance of the F11R function in the initiation of inflammatory thrombosis.