TY - JOUR
T1 - Two genes, COL4A3 and COL4A4 coding for the human α3(IV) and α4(IV) collagen chains are arranged head-to-head on chromosome 2q36
AU - Momota, Ryusuke
AU - Sugimoto, Manabu
AU - Oohashi, Toshitaka
AU - Kigasawa, Kazuteru
AU - Yoshioka, Hidekatsu
AU - Ninomiya, Yoshifumi
N1 - Funding Information:
This work was supported in part by Scientific Research Grant, Grant-In-Aid for Exploratory Research 08877098 (to R.M.) and Grant-In-Aid for Scientific Research (B) 08457154 (to Y.N.) from the Ministry of Education, Science, and Culture of Japan, and The Nakatomi Foundation.
PY - 1998/3/6
Y1 - 1998/3/6
N2 - We first isolated and characterized genomic DNA fragments that cover the 5' flanking sequences of COL4A3 and COL4A4 encoding the human basement membrane α3(IV) and α4(IV) collagen chains, respectively. Nucleotide sequence analysis indicated that the two genes are arranged head-to-head. To determine transcription start site for COL4A4 gene, we performed RACE and RNase protection assays, indicating that there are two alternative transcripts presumably derived from two different promoters. Interestingly, one transcription start site (from exon 1') of COL4A4 is only 5 bp away from the reported transcription start site of COL4A3, whereas the other transcript (from exon 1) starts 373 nucleotides downstream from the first one, generating the two kinds of transcripts that differ in the 5' UTR regions. Expression of these two transcripts appears tissue-specific; exon 1 transcript was expressed predominantly in epithelial cells, while exon 1' transcript showed rather ubiquitous and low expression. The nucleotide sequence of the promoter region is composed of dense CpG dinucleotides, GC boxes, CTC boxes and a CCAAT box but no TATA box. These results provide information to delineate the promoter activity for the tissue-specific expression of the six type IV collagen genes and basement membrane assembly in different tissues and organs.
AB - We first isolated and characterized genomic DNA fragments that cover the 5' flanking sequences of COL4A3 and COL4A4 encoding the human basement membrane α3(IV) and α4(IV) collagen chains, respectively. Nucleotide sequence analysis indicated that the two genes are arranged head-to-head. To determine transcription start site for COL4A4 gene, we performed RACE and RNase protection assays, indicating that there are two alternative transcripts presumably derived from two different promoters. Interestingly, one transcription start site (from exon 1') of COL4A4 is only 5 bp away from the reported transcription start site of COL4A3, whereas the other transcript (from exon 1) starts 373 nucleotides downstream from the first one, generating the two kinds of transcripts that differ in the 5' UTR regions. Expression of these two transcripts appears tissue-specific; exon 1 transcript was expressed predominantly in epithelial cells, while exon 1' transcript showed rather ubiquitous and low expression. The nucleotide sequence of the promoter region is composed of dense CpG dinucleotides, GC boxes, CTC boxes and a CCAAT box but no TATA box. These results provide information to delineate the promoter activity for the tissue-specific expression of the six type IV collagen genes and basement membrane assembly in different tissues and organs.
KW - Alternative transcription
KW - Basement membrane
KW - COL4A3
KW - COL4A4
KW - Synteny
KW - Type IV collagen
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U2 - 10.1016/S0014-5793(98)00128-8
DO - 10.1016/S0014-5793(98)00128-8
M3 - Article
C2 - 9537506
AN - SCOPUS:0032489425
SN - 0014-5793
VL - 424
SP - 11
EP - 16
JO - FEBS Letters
JF - FEBS Letters
IS - 1-2
ER -