EVOLUTION OF GENE-REGULATION AS REVEALED BY DIFFERENTIAL REGULATION OF THE CHICKEN LYSOZYME TRANSGENE AND THE ENDOGENOUS MOUSE LYSOZYME GENE IN MOUSE MACROPHAGES

被引:27
作者
BONIFER, C [1 ]
BOSCH, FX [1 ]
FAUST, N [1 ]
SCHUHMANN, A [1 ]
SIPPEL, AE [1 ]
机构
[1] UNIV HEIDELBERG, HALS NASEN OHREN KLIN, W-6900 HEIDELBERG, GERMANY
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1994年 / 226卷 / 01期
关键词
D O I
10.1111/j.1432-1033.1994.tb20045.x
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
Lysozyme gene expression is a marker for macrophage differentiation in vertebrates. We have previously shown that expression of the complete chicken lysozyme gene domain in macrophages of transgenic mice is directly correlated to the copy number of integrated transgenes. Thus, the chicken lysozyme locus in the mouse acts as an independent regulatory unit irrespective of its random position in the host genome. This finding allowed a comparative analysis of the regulation of the endogenous mouse lysozyme M gene and the chicken lysozyme transgene in the same animal. We demonstrate by transcript analysis of total tissue RNA and by in situ hybridization, that both genes are expressed in macrophages. In macrophages of the same animal the regulation of both genes in response to external signals was distinctly different: the lysozyme transgene responded to various agents influencing macrophage activation, in contrast, mouse lysozyme RNA levels remained unchanged under these conditions. Thus, as in chicken macrophages, the chicken lysozyme expression level in mouse macrophages is coupled to the macrophage activation status, while the mouse lysozyme is not. Our results suggest, that the cis-regulatory elements of lysozyme genes have evolved more rapidly than the function and expression of the trans-acting factors involved in the regulation of macrophage-specific gene activation.
引用
收藏
页码:227 / 235
页数:9
相关论文
共 55 条
[11]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[12]   CLONING THE HUMAN LYSOZYME CDNA - INVERTED ALU REPEAT IN THE MESSENGER-RNA AND INSITU HYBRIDIZATION FOR MACROPHAGES AND PANETH CELLS [J].
CHUNG, LP ;
KESHAV, S ;
GORDON, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (17) :6227-6231
[13]   NUMBER AND EVOLUTIONARY CONSERVATION OF ALPHA-TUBULIN AND BETA-TUBULIN AND CYTOPLASMIC BETA-ACTIN AND GAMMA-ACTIN GENES USING SPECIFIC CLONED CDNA PROBES [J].
CLEVELAND, DW ;
LOPATA, MA ;
MACDONALD, RJ ;
COWAN, NJ ;
RUTTER, WJ ;
KIRSCHNER, MW .
CELL, 1980, 20 (01) :95-105
[14]   RECENT ORIGIN OF THE P-LYSOZYME GENE IN MICE [J].
CORTOPASSI, GA ;
WILSON, AC .
NUCLEIC ACIDS RESEARCH, 1990, 18 (07) :1911-1911
[15]   MOUSE LYSOZYME-M GENE - ISOLATION, CHARACTERIZATION, AND EXPRESSION STUDIES [J].
CROSS, M ;
MANGELSDORF, I ;
WEDEL, A ;
RENKAWITZ, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (17) :6232-6236
[16]   REPETITIVE SEQUENCE INVOLVEMENT IN THE DUPLICATION AND DIVERGENCE OF MOUSE LYSOZYME GENES [J].
CROSS, M ;
RENKAWITZ, R .
EMBO JOURNAL, 1990, 9 (04) :1283-1288
[17]   AN IN-VITRO DIFFERENTIATION SYSTEM FOR THE EXAMINATION OF TRANSGENE ACTIVATION IN MOUSE MACROPHAGES [J].
FAUST, N ;
BONIFER, C ;
WILES, MV ;
SIPPEL, AE .
DNA AND CELL BIOLOGY, 1994, 13 (09) :901-907
[18]   ALTERNATIVE SETS OF DNASE I-HYPERSENSITIVE SITES CHARACTERIZE THE VARIOUS FUNCTIONAL-STATES OF THE CHICKEN LYSOZYME GENE [J].
FRITTON, HP ;
IGOKEMENES, T ;
NOWOCK, J ;
STRECHJURK, U ;
THEISEN, M ;
SIPPEL, AE .
NATURE, 1984, 311 (5982) :163-165
[19]   DNASE I-HYPERSENSITIVE SITES IN THE CHROMATIN STRUCTURE OF THE LYSOZYME GENE IN STEROID-HORMONE TARGET AND NONTARGET CELLS [J].
FRITTON, HP ;
IGOKEMENES, T ;
NOWOCK, J ;
STRECHTURK, U ;
THEISEN, M ;
SIPPEL, AE .
BIOLOGICAL CHEMISTRY HOPPE-SEYLER, 1987, 368 (02) :111-119
[20]   INVITRO SYNTHESIS AND SECRETION OF LYSOZYME BY MONONUCLEAR PHAGOCYTES [J].
GORDON, S ;
TODD, J ;
COHN, ZA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1974, 139 (05) :1228-1248