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Cited by 95

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Human group-specific component (Gc) is a member of the albumin family.

Yang, F, Brune, J L, Naylor, S L, Cupples, R L, Naberhaus, K H, Bowman, B H·1985·Proceedings of the National Academy of Sciences

Abstract

The group-specific component (Gc) is the major vitamin D-binding protein in plasma. The gene encoding Gc is linked, on human chromosome 4, to the albumin and alpha-fetoprotein genes. These two genes previously were shown to have evolved from a smaller ancestral gene by intragenic triplication. Recombinant plasmids containing human cDNA encoding Gc have been isolated by screening an adult human liver library with a mixed oligonucleotide probe. Characterization of Gc cDNA has provided the complete amino acid sequence of the protein and revealed strong sequence homology with albumin and alpha-fetoprotein. Of particular interest is a conserved pattern of disulfide bridges that form the triple-domain structures in albumin, alpha-fetoprotein, and Gc. Gc cDNA was used as a probe in Southern blot analysis of somatic-cell hybrids to confirm that the Gc locus is on chromosome 4.

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Metadata

Authors
Yang, F., Brune, J. L., Naylor, S. L., Cupples, R. L., Naberhaus, K. H., & Bowman, B. H.
Venue
Proceedings of the National Academy of Sciences
Published
1985-12
Volume
82
Issue
23
Pages
7994-7998
ISSN
  • 0027-8424
  • 1091-6490
Cited by
95
References
0
Language
en

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CoChat. (2026). Citation check: Human group-specific component (Gc) is a member of the albumin family. https://app.cochat.ai/papers/10.1073/pnas.82.23.7994
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Yang, F., Brune, J. L., Naylor, S. L., Cupples, R. L., Naberhaus, K. H., & Bowman, B. H. (1985). Human group-specific component (Gc) is a member of the albumin family. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.82.23.7994

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.