Cloning, sequence and expression of human interleukin-2 receptor.

Abstract:

:T lymphocytes, essential for the generation of a normal immune response, require the presence of the lymphokine interleukin-2 (IL-2) in order to proliferate. Cells that respond to IL-2 possess a surface receptor glycoprotein specific for this lymphokine. We have recently purified and chemically characterized the IL-2 receptor from both phytohaemagglutinin-activated human T cells and the human T-cell lymphoma HUT-102 (ref. 5). From the NH2-terminal protein sequence obtained in that study, we have now used synthetic oligonucleotides to probe a complementary DNA library, prepared from HUT-102 messenger RNA, for the presence of cDNA clones that might code for the IL-2 receptor. Two cDNA clones were isolated which had closely related DNA sequences. Interestingly, only one coded for an active receptor when transfected into COS-7 cells. This clone contained a 216-base pair (bp) insert that was not present in the other clone. The insert was flanked by an 8-bp direct repeat reminiscent of a transposable element, and appeared to code for a region of marked structural homology to the NH2-terminal region of the receptor molecule.

journal_name

Nature

journal_title

Nature

authors

Cosman D,Cerretti DP,Larsen A,Park L,March C,Dower S,Gillis S,Urdal D

doi

10.1038/312768a0

subject

Has Abstract

pub_date

1984-12-20 00:00:00

pages

768-71

issue

5996

eissn

0028-0836

issn

1476-4687

journal_volume

312

pub_type

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