CHROMOSOMAL LOCALIZATION OF 3 PULMONARY SURFACTANT PROTEIN GENES IN THE MOUSE

被引:45
作者
MOORE, KJ
DAMOREBRUNO, MA
KORFHAGEN, TR
GLASSER, SW
WHITSETT, JA
JENKINS, NA
COPELAND, NG
机构
[1] NCI,FREDERICK CANC RES & DEV CTR,ABL BASIC RES PROGRAM,MAMMALIAN GENET LAB,POB B,BLDG 539,FREDERICK,MD 21702
[2] CHILDRENS HOSP,MED CTR,COLL MED,DIV PULM BIOL,CINCINNATI,OH 45267
关键词
D O I
10.1016/0888-7543(92)90389-A
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Pulmonary surfactant, a protein-phospholipid mixture, maintains surface tension at the lung epithelium/air interface preventing alveolar collapse during respiration. For mammals appropriate developmental production of surfactant is necessary for adaptation to the air breathing environment. Deficiency of pulmonary surfactant results in respiratory distress syndrome (RDS), a leading cause of death in premature infants. Recently, three lung-specific pulmonary surfactant proteins designated SP-A, SP-B, and SP-C have been described. Cloned sequences for the genes that encode each of these proteins have been partially characterized in humans and other species. Analysis of interspecific backcross mice has allowed us to map the chromosomal locations of these three genes in the mouse. The gene encoding SP-A (Sftp-1) and the gene encoding SP-C (Sftp-2) both map to mouse chromosome 14, although at separate locations, while the gene encoding SP-B (Sftp-3) maps to chromosome 6. The mouse map locations determined in this study for the Sftp genes are consistent with the locations of these genes on the human genetic map and the syntenic relationships between the human and the mouse genomes. © 1992.
引用
收藏
页码:388 / 393
页数:6
相关论文
共 67 条
[1]   SURFACE PROPERTIES IN RELATION TO ATELECTASIS AND HYALINE MEMBRANE DISEASE [J].
AVERY, ME ;
MEAD, J .
AMA JOURNAL OF DISEASES OF CHILDREN, 1959, 97 (05) :517-523
[2]   GENETIC-ANALYSIS OF THE MOUSE USING INTERSPECIFIC CROSSES [J].
AVNER, P ;
AMAR, L ;
DANDOLO, L ;
GUENET, JL .
TRENDS IN GENETICS, 1988, 4 (01) :18-23
[3]  
BENSON B, 1985, P NATL ACAD SCI USA, V82, P3679
[4]   STRUCTURE AND EXPRESSION OF THE MURINE RETINOBLASTOMA GENE AND CHARACTERIZATION OF ITS ENCODED PROTEIN [J].
BERNARDS, R ;
SCHACKLEFORD, GM ;
GERBER, MR ;
HOROWITZ, JM ;
FRIEND, SH ;
SCHARTL, M ;
BOGENMANN, E ;
RAPAPORT, JM ;
MCGEE, T ;
DRYJA, TP ;
WEINBERG, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (17) :6474-6478
[5]  
BOGGARAM V, 1988, J BIOL CHEM, V263, P2939
[6]   BIOCHEMICAL DIVERSITY AND EVOLUTION IN THE GENUS MUS [J].
BONHOMME, F ;
CATALAN, J ;
BRITTONDAVIDIAN, J ;
CHAPMAN, VM ;
MORIWAKI, K ;
NEVO, E ;
THALER, L .
BIOCHEMICAL GENETICS, 1984, 22 (3-4) :275-303
[7]   THE HUMAN HOMOLOGS OF THE RAF (MIL) ONCOGENE ARE LOCATED ON HUMAN CHROMOSOME-3 AND CHROMOSONE-4 [J].
BONNER, T ;
OBRIEN, SJ ;
NASH, WG ;
RAPP, UR ;
MORTON, CC ;
LEDER, P .
SCIENCE, 1984, 223 (4631) :71-74
[8]  
BOWCOCK AM, 1988, AM J HUM GENET, V43, P664
[9]  
BRUNS G, 1987, HUM GENET, V76, P58
[10]  
BUCHBERG AM, 1988, ONCOGENE RES, V2, P149