RETINA-SPECIFIC EXPRESSION FROM THE IRBP PROMOTER IN TRANSGENIC MICE IS CONFERRED BY 212 BP OF THE 5'-FLANKING REGION

被引:35
作者
LIOU, GI
MATRAGOON, S
YANG, J
GENG, L
OVERBEEK, PA
MA, DP
机构
[1] MISSISSIPPI STATE UNIV, DEPT BIOCHEM & MOLEC BIOL, MISSISSIPPI STATE, MS 39762 USA
[2] MED COLL GEORGIA, DEPT BIOCHEM & MOLEC BIOL, AUGUSTA, GA 30912 USA
[3] HOSP SICK CHILDREN, DEPT RHEUMATOL, TORONTO M5G 1X8, ONTARIO, CANADA
[4] BAYLOR COLL MED, HOWARD HUGHES MED INST, HOUSTON, TX 77030 USA
[5] BAYLOR COLL MED, DEPT CELL BIOL, HOUSTON, TX 77030 USA
[6] BAYLOR COLL MED, DEPT OPHTHALMOL, HOUSTON, TX 77030 USA
[7] BAYLOR COLL MED, DIV NEUROSCI, HOUSTON, TX 77030 USA
关键词
D O I
10.1016/S0006-291X(05)81395-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
IRBP is a photoreceptor-specific glycoprotein that has been suggested as a retinoid carrier in the visual process. Previous research has shown that 1.3 kb of 5′-flanking sequence from the human IRBP gene is sufficient to promote photoreceptor-specific expression of reporter genes in transgenic mice. To define more narrowly the sequences that promote tissue-specific expression, chimeric constructs with shorter promoters were used to generate transgenic mice. The bacterial CAT gene was fused to fragments of 706 bp or 212 bp from the 5′ end of the human IRBP gene. Analysis of the three transgenic families bearing the 706 bp IRBP promoter revealed that CAT expression was confined to the neuro-retina and the pineal gland. Analysis of the four transgenic families bearing the 212 bp IRBP promoter revealed the same tissue-specific CAT expression in three families. These results establish that tissue-specific expression of IRBP can be regulated by a short 212 bp promoter which has been conserved between humans and mice. © 1991 Academic Press, Inc.
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收藏
页码:159 / 165
页数:7
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