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Cited by 157Connective tissue disorders researchMetabolism and Genetic DisordersCollagen: Extraction and Characterization

The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.

Lysyl-Protocollagen Hydroxylase Deficiency in Fibroblasts from Siblings with Hydroxylysine-Deficient Collagen

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Krane, S. M., Pinnell, S. R., Erbe, R. W.·1972·Proceedings of the National Academy of Sciences
DOI 10.1073/pnas.69.10.2899PMC PMC389670
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Abstract

Cell culture studies were performed on members of a family in which two sisters, ages 9 and 12, have a similar disorder characterized clinically by severe scoliosis, joint laxity and recurrent dislocations, hyperextensible skin, and thin scars. The skin collagen from the sisters was markedly deficient in hydroxylysine, but other amino acids were present in normal amounts. Hydroxylysine in collagen from fascia and bone was reduced to a lesser extent. Since the most likely explanation for the hydroxylysine deficiency was a reduction in enzymatic hydroxylation of lysine residues in protocollagen, we measured the activity of lysyl-protocollagen hydroxylase in crude lysates of cultured skin fibroblasts. Enzyme activities in the two affected children were 14 and 10% of controls, whereas the activity was about 60% of normal in the mother, a pattern most consistent with autosomal recessive inheritance. The mutant enzyme demonstrated the same cofactor requirements as that from normal cells. Deficiency of lysyl-protocollagen hydroxylase is the first inborn error of human collagen metabolism to be defined at the biochemical level.

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Metadata

Authors
Krane, S. M., Pinnell, S. R., & Erbe, R. W.
Affiliations
Harvard University (US)
Venue
Proceedings of the National Academy of Sciences
Publisher
National Academy of Sciences
Published
1972-10
Volume
69
Issue
10
Pages
2899-2903
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
DOI
10.1073/pnas.69.10.2899
PMC
PMC389670
OpenAlex
W1987968808
Cited by
157
References
27
Citations by year
2026: 1 · 2024: 2 · 2022: 2 · 2021: 5 · 2020: 4 · 2019: 1 · 2018: 3 · 2017: 2 · 2015: 3 · 2014: 2 · 2013: 2 · 2012: 2
FWCI
5.47
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Helen Hay Whitney Foundation
  • U.S. Public Health Service
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Connective tissue disorders research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
  • Physical Sciences › Materials Science › Biomaterials › Collagen: Extraction and Characterization
Keywords
lysine hydroxylation, collagen metabolism, inborn errors of metabolism, autosomal recessive inheritance, fibroblasts, scoliosis, joint laxity
MeSH terms
Adolescent, Adult, Amino Acids, Cells, Cultured, Child, Collagen, Consanguinity, Ehlers-Danlos Syndrome, Female, Fibroblasts, Humans, Hydrogen-Ion Concentration, Mixed Function Oxygenases, Hydroxylysine, L-Lactate Dehydrogenase, Lysine, Male, Metabolism, Inborn Errors, Methyltransferases, Proline, Procollagen-Proline Dioxygenase, Protein Precursors, Serine, Skin, Time Factors

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