TY - JOUR
T1 - Chromosomal localization of three pulmonary surfactant protein genes in the mouse
AU - Moore, Karen J.
AU - D'Amore-Bruno, Melanie A.
AU - Korfhagen, Thomas R.
AU - Glasser, Stephan W.
AU - Whitsett, Jeffrey A.
AU - Jenkins, Nancy A.
AU - Copeland, Neal G.
N1 - Funding Information:
We thank Linda Brubaker for typing the manuscript. This work was supported by the National Cancer Institute, DHHS, under Contract No. NOl-CO-74101 with ABL (K.J.M., N.A.J., N.G.C.) and by National Institutes of Health Grants HL28623 (J.A.W.) and HL3859 (J.A.W.). M.A.D’A.-B. was supported by a Molecular and Cellular Biology Training Grant, NIH HL7527, and an American Lung Association Grant.
PY - 1992/2
Y1 - 1992/2
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=0026549894&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0026549894&partnerID=8YFLogxK
U2 - 10.1016/0888-7543(92)90389-A
DO - 10.1016/0888-7543(92)90389-A
M3 - Article
C2 - 1346779
AN - SCOPUS:0026549894
SN - 0888-7543
VL - 12
SP - 388
EP - 393
JO - Genomics
JF - Genomics
IS - 2
ER -