HORMONAL MODULATION OF A GENE INJECTED INTO RAT-HEART INVIVO

被引:163
作者
KITSIS, RN
BUTTRICK, PM
MCNALLY, EM
KAPLAN, ML
LEINWAND, LA
机构
[1] YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT MED, BRONX, NY 10461 USA
[2] MONTEFIORE MED CTR, BRONX, NY 10467 USA
关键词
CARDIAC GENE TRANSFER; TRANSFECTION; GENE REGULATION; THYROID HORMONE; MYOSIN HEAVY CHAIN;
D O I
10.1073/pnas.88.10.4138
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We demonstrate gene transfer into rat heart in vivo by the direct injection of plasmid DNA. Injection of gene constructs driven by retroviral and cellular promoters resulted in detectable levels of reporter gene activities. The cellular promoter and 5' flanking sequence (positions -613 to +32) were derived from the rat alpha-myosin heavy chain gene whose expression in vivo is restricted to cardiac muscle and is positively regulated by thyroid hormone. After DNA injection, activity of the firefly luciferase gene coupled to the myosin heavy chain promoter and regulatory sequence was detected in heart but not in skeletal muscle and was significantly increased in response to thyroid hormone treatment. Consequently, expression of injected genes can be targeted to specific cell types in vivo and can be modulated by the hormonal status of the animal. This approach provides a means of mapping the elements of genes that regulate their responses to complex stimuli that cannot be modeled in vitro.
引用
收藏
页码:4138 / 4142
页数:5
相关论文
共 29 条
[1]  
ACSADI G, 1991, NEW BIOL, V3, P71
[2]  
BRASIER AR, 1989, BIOTECHNIQUES, V7, P1116
[3]  
CHIZZONITE RA, 1984, J BIOL CHEM, V259, P2628
[4]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[5]   PROGRESS TOWARD HUMAN-GENE THERAPY [J].
FRIEDMANN, T .
SCIENCE, 1989, 244 (4910) :1275-1281
[6]   THE ROUS-SARCOMA VIRUS LONG TERMINAL REPEAT IS A STRONG PROMOTER WHEN INTRODUCED INTO A VARIETY OF EUKARYOTIC CELLS BY DNA-MEDIATED TRANSFECTION [J].
GORMAN, CM ;
MERLINO, GT ;
WILLINGHAM, MC ;
PASTAN, I ;
HOWARD, BH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (22) :6777-6781
[7]   THYROID-HORMONE REGULATES EXPRESSION OF A TRANSFECTED ALPHA-MYOSIN HEAVY-CHAIN FUSION GENE IN FETAL HEART-CELLS [J].
GUSTAFSON, TA ;
MARKHAM, BE ;
BAHL, JJ ;
MORKIN, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (10) :3122-3126
[8]   DIVERSITY OF ALPHA-FETOPROTEIN GENE-EXPRESSION IN MICE IS GENERATED BY A COMBINATION OF SEPARATE ENHANCER ELEMENTS [J].
HAMMER, RE ;
KRUMLAUF, R ;
CAMPER, SA ;
BRINSTER, RL ;
TILGHMAN, SM .
SCIENCE, 1987, 235 (4784) :53-58
[9]   DIFFERENTIAL RESPONSE TO L-TRIIODOTHYRONINE OF ANTERIOR-PITUITARY GROWTH-HORMONE MESSENGER-RIBONUCLEIC-ACID (MESSENGER-RNA) AND BETA-THYROTROPIN MESSENGER-RNA IN A HYPOTHYROID WALKER 256 CARCINOMA-BEARING RAT MODEL OF NONTHYROIDAL DISEASE [J].
HUPART, KH ;
DEFESI, CR ;
KATZ, CP ;
SHAPIRO, LE ;
SURKS, MI .
ENDOCRINOLOGY, 1990, 126 (01) :616-621
[10]   ALL MEMBERS OF THE MHC MULTIGENE FAMILY RESPOND TO THYROID-HORMONE IN A HIGHLY TISSUE-SPECIFIC MANNER [J].
IZUMO, S ;
NADALGINARD, B ;
MAHDAVI, V .
SCIENCE, 1986, 231 (4738) :597-600