TY - JOUR
T1 - The genes for a mouse hematopoietic differentiation marker called the heat‐stable antigen
AU - Wenger, Roland H.
AU - Ayane, Mohamed
AU - Bose, Ron
AU - Köhler, Georges
AU - Nielsen, Peter J.
PY - 1991/4
Y1 - 1991/4
N2 - We have isolated a murine cDNA by virtue of its expression in pre‐B cell lines but not in plasmacytomas. In mouse, mRNA is detected by Northern blot analysis exclusively in hematopoietic tissues with the exception of brain. When expressed in bacteria, the encoded protein is specifically recognized by several antibodies against the murine hematopoietic differentiation marker called heat‐stable antigen (HSA). In contrast to previous speculations, these results suggest that the antigenic determinant recognized by anti‐HSA antibodies is proteinaceous. The cDNA sequence is essentially identical to a mouse HSA cDNA recently published (Kay et al., J. Immunol. 1990. 145: 1952). Three HSA genes were isolated, one of which corresponds to the isolated cDNA. The other two appear to be intronless retroposons which, despite numerous sequence changes, maintain an open reading frame. One of these intronless genes could code for an alternative form of HSA with a transmembrane domain and a cytoplasmic tail not encoded by the intron‐containing gene. This gene could be expressed, based on sequence comparisons of the three genes. However, using polymerase chain reaction amplification of first strand cDNA from various cell lines and adult mouse tissues, we could detect expression only of the intron‐containing gene.
AB - We have isolated a murine cDNA by virtue of its expression in pre‐B cell lines but not in plasmacytomas. In mouse, mRNA is detected by Northern blot analysis exclusively in hematopoietic tissues with the exception of brain. When expressed in bacteria, the encoded protein is specifically recognized by several antibodies against the murine hematopoietic differentiation marker called heat‐stable antigen (HSA). In contrast to previous speculations, these results suggest that the antigenic determinant recognized by anti‐HSA antibodies is proteinaceous. The cDNA sequence is essentially identical to a mouse HSA cDNA recently published (Kay et al., J. Immunol. 1990. 145: 1952). Three HSA genes were isolated, one of which corresponds to the isolated cDNA. The other two appear to be intronless retroposons which, despite numerous sequence changes, maintain an open reading frame. One of these intronless genes could code for an alternative form of HSA with a transmembrane domain and a cytoplasmic tail not encoded by the intron‐containing gene. This gene could be expressed, based on sequence comparisons of the three genes. However, using polymerase chain reaction amplification of first strand cDNA from various cell lines and adult mouse tissues, we could detect expression only of the intron‐containing gene.
UR - http://www.scopus.com/inward/record.url?scp=0025909389&partnerID=8YFLogxK
U2 - 10.1002/eji.1830210427
DO - 10.1002/eji.1830210427
M3 - Article
C2 - 2019286
AN - SCOPUS:0025909389
SN - 0014-2980
VL - 21
SP - 1039
EP - 1046
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 4
ER -