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Pregled bibliografske jedinice broj: 1265357

Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked


Dohr, Katrin A.; Tokic, Silvija; Gastager-Ehgartner, Magdalena; Stojakovic, Tatjana; Dumic, Miroslav; Plecko, Barbara; Dumic, Katja K.
Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked // International Journal of Molecular Sciences, 24 (2023), 6; 5957, 11 doi:10.3390/ijms24065957 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 1265357 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked
(Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked Adrenoleukodystrophy)

Autori
Dohr, Katrin A. ; Tokic, Silvija ; Gastager-Ehgartner, Magdalena ; Stojakovic, Tatjana ; Dumic, Miroslav ; Plecko, Barbara ; Dumic, Katja K.

Izvornik
International Journal of Molecular Sciences (1422-0067) 24 (2023), 6; 5957, 11

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
X-linked adrenoleukodystrophy ; adrenomyeloneuropathy ; pathogenic variant

Sažetak
X-linked adrenoleukodystrophy (X-ALD) is a rare inborn error of the peroxisomal metabolism caused by pathologic variants in the ATP-binding cassette transporter type D, member 1 (ABCD1) gene located on the X-chromosome. ABCD1 protein, also known as adrenoleukodystrophy protein, is responsible for transport of the very long chain fatty acids (VLCFA) from cytoplasm into the peroxisomes. Therefore, altered function or lack of the ABCD1 protein leads to accumulation of VLCFA in various tissues and blood plasma leading to either rapidly progressive leukodystrophy (cerebral ALD), progressive adrenomyeloneuropathy (AMN), or isolated primary adrenal insufficiency (Addison’s disease). We report two distinct single nucleotide deletions in the ABCD1 gene, c.253delC [p.Arg85Glyfs*18] in exon 1, leading to both cerebral ALD and to AMN phenotype in one family, and c.1275delA [p.Phe426Leufs*15] in exon 4, leading to AMN and primary adrenal insufficiency in a second family. For the latter variant, we demonstrate reduced mRNA expression and a complete absence of the ABCD1 protein in PBMC. Distinct mRNA and protein expression in the index patient and heterozygous carriers does not associate with VLCFA concentration in plasma, which is in line with the absence of genotype–phenotype correlation in X-ALD.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)



POVEZANOST RADA


Ustanove:
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb

Profili:

Avatar Url Miroslav Dumić (autor)

Avatar Url Katja Dumić Kubat (autor)

Poveznice na cjeloviti tekst rada:

doi www.ncbi.nlm.nih.gov

Citiraj ovu publikaciju:

Dohr, Katrin A.; Tokic, Silvija; Gastager-Ehgartner, Magdalena; Stojakovic, Tatjana; Dumic, Miroslav; Plecko, Barbara; Dumic, Katja K.
Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked // International Journal of Molecular Sciences, 24 (2023), 6; 5957, 11 doi:10.3390/ijms24065957 (međunarodna recenzija, članak, znanstveni)
Dohr, K., Tokic, S., Gastager-Ehgartner, M., Stojakovic, T., Dumic, M., Plecko, B. & Dumic, K. (2023) Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked. International Journal of Molecular Sciences, 24 (6), 5957, 11 doi:10.3390/ijms24065957.
@article{article, author = {Dohr, Katrin A. and Tokic, Silvija and Gastager-Ehgartner, Magdalena and Stojakovic, Tatjana and Dumic, Miroslav and Plecko, Barbara and Dumic, Katja K.}, year = {2023}, pages = {11}, DOI = {10.3390/ijms24065957}, chapter = {5957}, keywords = {X-linked adrenoleukodystrophy, adrenomyeloneuropathy, pathogenic variant}, journal = {International Journal of Molecular Sciences}, doi = {10.3390/ijms24065957}, volume = {24}, number = {6}, issn = {1422-0067}, title = {Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked}, keyword = {X-linked adrenoleukodystrophy, adrenomyeloneuropathy, pathogenic variant}, chapternumber = {5957} }
@article{article, author = {Dohr, Katrin A. and Tokic, Silvija and Gastager-Ehgartner, Magdalena and Stojakovic, Tatjana and Dumic, Miroslav and Plecko, Barbara and Dumic, Katja K.}, year = {2023}, pages = {11}, DOI = {10.3390/ijms24065957}, chapter = {5957}, keywords = {X-linked adrenoleukodystrophy, adrenomyeloneuropathy, pathogenic variant}, journal = {International Journal of Molecular Sciences}, doi = {10.3390/ijms24065957}, volume = {24}, number = {6}, issn = {1422-0067}, title = {Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked Adrenoleukodystrophy}, keyword = {X-linked adrenoleukodystrophy, adrenomyeloneuropathy, pathogenic variant}, chapternumber = {5957} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Citati:





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