IDENTIFICATION AND CHARACTERIZATION OF A NOVEL TRANSCRIPTIONAL SILENCER IN THE HUMAN COLLAGEN TYPE-IV GENE COL4A2

Citation
A. Haniel et al., IDENTIFICATION AND CHARACTERIZATION OF A NOVEL TRANSCRIPTIONAL SILENCER IN THE HUMAN COLLAGEN TYPE-IV GENE COL4A2, The Journal of biological chemistry, 270(19), 1995, pp. 11209-11215
Citations number
54
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
270
Issue
19
Year of publication
1995
Pages
11209 - 11215
Database
ISI
SICI code
0021-9258(1995)270:19<11209:IACOAN>2.0.ZU;2-#
Abstract
Collagen type IV [alpha 1(IV)(2) alpha 2(IV)] is the basic structural component of all basement membranes. The two subunit genes COL4A1 and COL4A2 are found closely linked in the human and murine genomes and ar e transcribed divergently from a common promoter, Previously, activati ng elements had been detected within both genes which are indispensabl e for efficient transcription. An additional negative regulatory eleme nt has now been identified within the third intron of the COL4A2 gene which is able to inhibit transcription of both COL4 genes from their s hared promoter, as well as the nonrelated herpes simplex virus thymidi ne kinase promoter. The element exerts its inhibitory effect largely i ndependently from its relative orientation and distance from the initi ation site of transcription. Therefore, the element represents a silen cer, which is named the ''COL4 silencer.'' The minimal functional sile ncer could be narrowed down by deletion mapping to a sequence element located within intron 3 of the COL4A2 gene. This motif is specifically recognized by a nuclear protein, named ''SILBF,'' and the binding sit e of which was determined by footprinting assays. Mutation studies and deletion analysis proved that the presence of this sequence element a nd its interaction with SILBF is not only essential but also sufficien t for the silencing function. We assume that the COL4 silencer plays a n important role in the control of overall expression and the balance of divergent transcription of both COL4 genes.