Редактирование: CNDP1 (раздел)

==Publications==

{{medline-entry
|title=Allelic variation in the [[CNDP1]] gene and its lack of association with longevity and coronary heart disease.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/16965804
|abstract=Carnosine, a cytoprotective dipeptide found at very high concentrations in skeletal muscle, heart and brain, is cleaved in blood by serum carnosinase which is encoded by the [[CNDP1]] gene. We recently found that homozygosity of a 5-leucine variant in the leader peptide of this enzyme protects diabetes mellitus patients against nephropathy. Hypothesising that the same allele could also be associated with longevity or a reduced incidence of cardiovascular problems, we examined the frequency of [[CNDP1]] alleles in German centenarians, patients with premature coronary heart disease, and matched controls. A total of 1382 individuals was investigated. The 5-leucine allele was the most common allele in all groups investigated. There was no difference in allele or genotype frequency between centenarians and their control group, or between cardiovascular patients and their control group. The recently identified functional carnosinase variant therefore does neither contribute to longevity nor protect against coronary heart disease in our probands. In addition to the known trinucleotide repeat alleles in the [[CNDP1]] gene, we detected a rare 8-leucine allele, a rare duplication, p.L13_V15dup, and a more common frameshift deletion, L17fsX20. Homozygosity for L17fsX20, estimated to have a prevalence of approximately 1:20,000, would be expected to cause carnosinaemia, an autosomal recessive trait with uncertain clinical relevance.
|mesh-terms=* Aged
* Aged, 80 and over
* Alleles
* Amino Acid Sequence
* Base Sequence
* Coronary Disease
* Dipeptidases
* Female
* Genetic Variation
* Humans
* Longevity
* Male
* Middle Aged
* Molecular Sequence Data

|full-text-url=https://sci-hub.do/10.1016/j.mad.2006.08.002
}}