A cDNA library has been constructed in the plasmid pBR322 using as template 12 S poly(A)-RNA isolated from spleen cells of a hyperimmunized Basilea rabbit. One of these cDNA-containing clones was used to determine the nucleotide sequence coding for the lambda light chain constant (C) region. The ded
The mink gene for the λ light immunoglobulin chain: Characterization of cDNA and chromosomal localization
✍ Scribed by T. M. Khlebodarova; N. M. Matveeva; O. L. Serov; A. M. Najakshin; E. S. Belousov; S. V. Bogachev; O. K. Baranov
- Publisher
- Springer-Verlag
- Year
- 1992
- Tongue
- English
- Weight
- 530 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0938-8990
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✦ Synopsis
A cDNA library from mink spleen was constructed by use of the phage hgtll. The library was screened using polyvalent serum raised against the mink immunoglobulin k chain. As a result, several clones expressing mink immunoglobulin h light chains were identified. Sequencing of one of the clones with an 803 bp insert was performed. The insert comprised nearly the entire coding region for the mature k light immunoglobulin gene with the exception of the leader polypeptide and several amino acids of the FR1 region of the V segment. Compared with the rabbit, mouse and human h light immunoglobulin genes, the homology of the cloned sequence was found to be highest relative to the rabbit gene. With the cloned mink cDNA containing the C-region only as a probe, the DNAs from mink-Chinese hamster hybrid clones were studied. The results of segregation analysis of this mink cDNA sequence and mink chromosomes in the mink-Chinese hamster clone panel allowed us to assign the gene for the k light immunoglobulin constant polypeptide (IGLC) to mink Chromosome (Chr) 4.
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