Abstract
The structural organization of the gene for the human cysteine-proteinase inhibitor cystatin C was studied. Restriction-endonuclease digests of human genomic DNA hybridized with human cystatin C cDNA and genomic probes produced patterns consistent with a single cystatin C gene and, also, the presence of six closely related sequences in the human genome. A 30 kb restriction map covering the genomic region of the cystatin C gene was constructed. The positions of three polymorphic restriction sites, found at examination of digests of genomic DNA from 79 subjects, were localized in the flanking regions of the gene. The gene was cloned and the nucleotide sequence of a 7.3 kb genomic segment was determined, containing the three exons of the cystatin C structural gene as well as 1.0 kb of 5'-flanking and 2.0 kb of 3'-flanking sequences. Northern-blot experiments revealed that the cystatin C gene is expressed in every human tissue examined, including kidney, liver, pancreas, intestine, stomach, antrum, lung and placenta. The highest cystatin C expression was seen in seminal vesicles. The apparently non-tissue-specific expression of this cysteine-proteinase inhibitor gene is discussed with respect to the structure of its 5'-flanking region, which shares several features with those of housekeeping genes.
MeSH Terms
Amino Acid Sequence
Base Sequence
Blotting, Northern
Cystatin C
Cystatins/biosynthesis,genetics
DNA Probes
Exons
Gene Expression
Genes
Humans
Male
Molecular Sequence Data
Multigene Family
Organ Specificity
RNA, Messenger/analysis
Restriction Mapping
Seminal Vesicles/metabolism
Chemicals
CST3 protein, human
Cystatin C
Cystatins
DNA Probes
RNA, Messenger
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Abrahamson M
Department of Clinical Chemistry, University Hospital, Lund, Sweden.
Olafsson I
Palsdottir A
Ulvsbäck M
Lundwall A
Jensson O
Grubb A
References (27)
27 references, click to expand
-
Abnormal metabolism of gamma-trace alkaline microprotein. The basic defect in hereditary cerebral hemorrhage with amyloidosis.
N Engl J Med. 1984 Dec 13;311(24):1547-9
PMID: 6390199
-
Isolation and amino acid sequence of SAP-1, an acidic protein of human whole saliva, and sequence homology with human gamma-trace.
J Biochem. 1984 Aug;96(2):489-98
PMID: 6501254
-
Structural organization of the human kininogen gene and a model for its evolution.
J Biol Chem. 1985 Jul 15;260(14):8610-7
PMID: 2989294
-
Amino acid sequence of the intracellular cysteine proteinase inhibitor cystatin B from human liver.
Biochem Biophys Res Commun. 1985 Sep 30;131(3):1187-92
PMID: 3902020
-
Characterization of a new cysteine proteinase inhibitor of human saliva, cystatin SN, which is immunologically related to cystatin S.
FEBS Lett. 1986 Mar 17;198(1):145-9
PMID: 3514272
-
CpG-rich islands and the function of DNA methylation.
Nature. 1986 May 15-21;321(6067):209-13
PMID: 2423876
-
Structure of the human neutrophil elastase gene.
J Biol Chem. 1988 Oct 15;263(29):14739-47
PMID: 2902087
-
Stroke in Icelandic patients with hereditary amyloid angiopathy is related to a mutation in the cystatin C gene, an inhibitor of cysteine proteases.
J Exp Med. 1989 May 1;169(5):1771-8
PMID: 2541223
-
The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20.
Hum Genet. 1989 Jun;82(3):223-6
PMID: 2567273
-
DNA binding specificity of steroid receptors.
Cell. 1989 Jun 30;57(7):1065-8
PMID: 2661016
-
Isolation of six cysteine proteinase inhibitors from human urine. Their physicochemical and enzyme kinetic properties and concentrations in biological fluids.
J Biol Chem. 1986 Aug 25;261(24):11282-9
PMID: 3488317
-
Nomenclature and classification of the proteins homologous with the cysteine-proteinase inhibitor chicken cystatin.
Biochem J. 1986 May 15;236(1):312
PMID: 3491603
-
Molecular cloning and sequence analysis of cDNA coding for the precursor of the human cysteine proteinase inhibitor cystatin C.
FEBS Lett. 1987 Jun 1;216(2):229-33
PMID: 3495457
-
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.
Anal Biochem. 1987 Apr;162(1):156-9
PMID: 2440339
-
Characterization and amino acid sequence of a new acidic cysteine proteinase inhibitor (cystatin SA) structurally closely related to cystatin S, from human whole saliva.
J Biochem. 1987 Oct;102(4):693-704
PMID: 3436950
-
Human cysteine-proteinase inhibitors: nucleotide sequence analysis of three members of the cystatin gene family.
Gene. 1987;61(3):329-38
PMID: 3446578
-
Purification, molecular cloning, and sequencing of salivary cystatin SA-1.
J Biol Chem. 1988 Jul 5;263(19):9381-7
PMID: 2837486
-
Mutation in cystatin C gene causes hereditary brain haemorrhage.
Lancet. 1988 Sep 10;2(8611):603-4
PMID: 2900981
-
Organization and expression of eucaryotic split genes coding for proteins.
Annu Rev Biochem. 1981;50:349-83
PMID: 6791577
-
Polymorphic DNA region adjacent to the 5' end of the human insulin gene.
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5759-63
PMID: 6272317
-
Human gamma-trace, a basic microprotein: amino acid sequence and presence in the adenohypophysis.
Proc Natl Acad Sci U S A. 1982 May;79(9):3024-7
PMID: 6283552
-
An interactive graphics program for comparing and aligning nucleic acid and amino acid sequences.
Nucleic Acids Res. 1982 May 11;10(9):2951-61
PMID: 7099970
-
Automation of the computer handling of gel reading data produced by the shotgun method of DNA sequencing.
Nucleic Acids Res. 1982 Aug 11;10(15):4731-51
PMID: 7133997
-
Buffer gradient gels and 35S label as an aid to rapid DNA sequence determination.
Proc Natl Acad Sci U S A. 1983 Jul;80(13):3963-5
PMID: 6575390
-
Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastroentero-pancreatic neuroendocrine protein, gamma trace.
J Exp Med. 1983 Aug 1;158(2):623-8
PMID: 6886625
-
Protein inhibitors of cysteine proteinases. III. Amino-acid sequence of cystatin from chicken egg white.
Hoppe Seylers Z Physiol Chem. 1983 Nov;364(11):1487-96
PMID: 6662498
-
Isolation of a human cDNA for alpha 2-thiol proteinase inhibitor and its identity with low molecular weight kininogen.
Biochemistry. 1984 Nov 20;23(24):5691-7
PMID: 6441591