The human transmembrane secretory component (poly-Ig receptor) : molecular cloning, restriction fragment length polymorphism and chromosomal sublocalization

The human transmembrane secretory component (SC) mediates glandular translocation of polymeric IgA and IgM into exocrine secretions. A 2898-bp cDNA clone, encoding the entire sequence of the human transmembrane SC, was isolated from a colonic adenocarcinoma cell line cDNA library. The deduced amino-...

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Veröffentlicht in:Human genetics 1991-10, Vol.87 (6), p.642-648
Hauptverfasser: KRAJCI, P, GRZESCHIK, K. H, GEURTS VAN KESSEL, A. H. M, OLAISEN, B, BRANDTZAEG, P
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Sprache:eng
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Zusammenfassung:The human transmembrane secretory component (SC) mediates glandular translocation of polymeric IgA and IgM into exocrine secretions. A 2898-bp cDNA clone, encoding the entire sequence of the human transmembrane SC, was isolated from a colonic adenocarcinoma cell line cDNA library. The deduced amino-acid sequence had a length of 764 residues and showed an overall similarity of 56% and 64% with the rabbit and rat counterpart, respectively. A restriction fragment length polymorphism (RFLP) was found with PvuII, revealing a two-alle RFLP with an autosomal codominant inheritance pattern and allele frequencies of 0.65 and 0.35. Southern blot analysis of human-rodent somatic hybrid panels, including hybrids with translocation chromosomes carrying different parts of chromosome 1, assigned the SC gene to 1q31-q42, thus confirming a previously reported provisional assignment.
ISSN:0340-6717
1432-1203
DOI:10.1007/bf00201717