Differential regulation of rat aquaporin-5 promoter/enhancer activities in lung and salivary epithelial cells

被引:35
作者
Barok, Z
Li, X
Fernandes, VFJ
Zhou, B
Ann, DK
Crandall, ED
机构
[1] Univ So Calif, Div Pulm & Crit Care Med, Dept Med, Los Angeles, CA 90033 USA
[2] Univ So Calif, Dept Mol Pharmacol & Toxicol, Will Rogers Inst Pulm Res Ctr, Los Angeles, CA 90033 USA
[3] Univ So Calif, Sch Med, Los Angeles, CA 90033 USA
[4] Univ So Calif, Sch Pharm, Los Angeles, CA 90033 USA
关键词
D O I
10.1074/jbc.M910007199
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
Aquaporin-5 (AQP5) is a water channel protein that is selectively expressed in respiratory, salivary, and lacrimal tissues. In order to establish the tissue-specific transcriptional programs that underlie its lung and salivary-specific expression, a 4,5-kilobase pair DNA fragment encompassing the 5'-flanking region of the rat AQP5 gene has been characterized in detail. A major transcription start site utilized in lung and salivary glands has been localized downstream of a TATAA-like motif, Transient transfection assays of -4,3- and -1.7-AQP5-luciferase constructs in AQP5-expressing lung (MLE-15) and salivary (Pa-4) cells and nonexpressing fibroblast (NIH3T3) and epithelial (HeLa) cells demonstrate preferential transcriptional enhancement of reporter activities in MLE-15 and Pa-4 cells. Transient transfection assays of a series of 5' -> 3' deletion constructs of -4.3-AQP5-luciferase suggest that a common salivary and lung enhancer is located between nucleotides -274 and -139, and a lung-specific enhancer is located between nucleotides -894 and -710. There is one putative lung-specific repressor located in the region of nucleotides -1003/-894 and a common lung and salivary repressor located at nucleotides -503/-385, Moreover, 3' -> 5' deletions up to -171 and -127 base pairs almost abolish transcriptional activation in salivary and lung cells, respectively. Together, our findings indicate that the combination of enhancer/repressor elements within the proximal 5'-flankinng region of rat AQP5 gene dictates its restricted expression in both lung and salivary cells.
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页码:26507 / 26514
页数:8
相关论文
共 55 条
[1]  
ADAMSON IYR, 1974, LAB INVEST, V30, P35
[2]   The aquaporins, blueprints for cellular plumbing systems [J].
Agre, P ;
Bonhivers, M ;
Borgnia, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (24) :14659-14662
[3]   Regulation of gene expression by alternative promoters [J].
Ayoubi, TAY ;
VanDeVen, WJM .
FASEB JOURNAL, 1996, 10 (04) :453-460
[4]   Nuclear factor I family members regulate the transcription of surfactant protein-C [J].
Bachurski, CJ ;
Kelly, SE ;
Glasser, SW ;
Currier, TA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (52) :32759-32766
[5]   THE LUNG-SPECIFIC SURFACTANT PROTEIN-B GENE PROMOTER IS A TARGET FOR THYROID TRANSCRIPTION FACTOR-1 AND HEPATOCYTE NUCLEAR FACTOR-3, INDICATING COMMON FACTORS FOR ORGAN-SPECIFIC GENE-EXPRESSION ALONG THE FOREGUT AXIS [J].
BOHINSKI, RJ ;
DILAURO, R ;
WHITSETT, JA .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (09) :5671-5681
[6]   Keratinocyte growth factor modulates alveolar epithelial cell phenotype in vitro:: Expression of aquaporin 5 [J].
Borok, Z ;
Lubman, RL ;
Danto, SI ;
Zhang, XL ;
Zabski, SM ;
King, LS ;
Lee, DM ;
Agre, P ;
Crandall, ED .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 18 (04) :554-561
[7]   Modulation of T1α expression With alveolar epithelial cell phenotype in vitro [J].
Borok, Z ;
Danto, SI ;
Lubman, RL ;
Cao, YX ;
Williams, MC ;
Crandall, ED .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1998, 275 (01) :L155-L164
[8]  
BOROK Z, 1994, IN VITRO CELL DEV-AN, V30A, P99
[9]   CELLULAR-DISTRIBUTION OF THE AQUAPORINS - A FAMILY OF WATER CHANNEL PROTEINS [J].
BROWN, D ;
KATSURA, T ;
KAWASHIMA, M ;
VERKMAN, AS ;
SABOLIC, I .
HISTOCHEMISTRY AND CELL BIOLOGY, 1995, 104 (01) :1-9
[10]   LUNG CELL-SPECIFIC EXPRESSION OF THE MURINE SURFACTANT PROTEIN-A (SP-A) GENE IS MEDIATED BY INTERACTIONS BETWEEN THE SP-A PROMOTER AND THYROID TRANSCRIPTION FACTOR-I [J].
BRUNO, MD ;
BOHINSKI, RJ ;
HUELSMAN, KM ;
WHITSETT, JA ;
KORFHAGEN, TR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (12) :6531-6536