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Pregled bibliografske jedinice broj: 627252

Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses


Sundström, Elisabeth; Imsland, Freyja; Mikko, Sofia; Wade, Claire; Sigurdsson, Snaevar; Pielberg, Gerli R; Golovko, Anna; Curik, Ino; Seltenhammer, Monika H; Sölkner, Johann et al.
Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses // Bmc genomics, 13 (2012), 13:365; 1-13 doi::10.1186/1471-2164-13-365 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 627252 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses

Autori
Sundström, Elisabeth ; Imsland, Freyja ; Mikko, Sofia ; Wade, Claire ; Sigurdsson, Snaevar ; Pielberg, Gerli R ; Golovko, Anna ; Curik, Ino ; Seltenhammer, Monika H ; Sölkner, Johann ; Lindblad-Toh, Kerstin ; Andersson, Leif

Izvornik
Bmc genomics (1471-2164) 13 (2012), 13:365; 1-13

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

Ključne riječi
STX17 ; Melanoma ; Hair greying ; Copy number variation ; Melanocytes

Sažetak
Background Greying with age in horses is an autosomal dominant trait, associated with loss of hair pigmentation, melanoma and vitiligo-like depigmentation. We recently identified a 4.6 kb duplication in STX17 to be associated with the phenotype. The aims of this study were to investigate if the duplication in Grey horses shows copy number variation and to exclude that any other polymorphism is uniquely associated with the Grey mutation. Results We found little evidence for copy number expansion of the duplicated sequence in blood DNA from Grey horses. In contrast, clear evidence for copy number expansions was indicated in five out of eight tested melanoma tissues or melanoma cell lines. A tendency of a higher copy number in aggressive tumours was also found. Massively parallel resequencing of the ~350 kb Grey haplotype did not reveal any additional mutations perfectly associated with the phenotype, confirming the duplication as the true causative mutation. We identified three SNP alleles that were present in a subset of Grey haplotypes within the 350 kb region that shows complete linkage disequilibrium with the causative mutation. Thus, these three nucleotide substitutions must have occurred subsequent to the duplication, consistent with our interpretation that the Grey mutation arose more than 2, 000 years before present. Conclusions These results suggest that the mutation acts as a melanoma-driving regulatory element. The elucidation of the mechanistic features of the duplication will be of considerable interest for the characterization of these horse melanomas as well as for the field of human melanoma research.

Izvorni jezik
Engleski

Znanstvena područja
Biologija, Veterinarska medicina, Poljoprivreda (agronomija)



POVEZANOST RADA


Projekti:
178-1780460-0546 - Strategije eliminacije genetskih defekata u selekcioniranim populacijama (Čurik, Ino, MZOS ) ( CroRIS)

Ustanove:
Agronomski fakultet, Zagreb

Profili:

Avatar Url Ino Čurik (autor)

Poveznice na cjeloviti tekst rada:

Pristup cjelovitom tekstu rada doi

Citiraj ovu publikaciju:

Sundström, Elisabeth; Imsland, Freyja; Mikko, Sofia; Wade, Claire; Sigurdsson, Snaevar; Pielberg, Gerli R; Golovko, Anna; Curik, Ino; Seltenhammer, Monika H; Sölkner, Johann et al.
Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses // Bmc genomics, 13 (2012), 13:365; 1-13 doi::10.1186/1471-2164-13-365 (međunarodna recenzija, članak, znanstveni)
Sundström, E., Imsland, F., Mikko, S., Wade, C., Sigurdsson, S., Pielberg, G., Golovko, A., Curik, I., Seltenhammer, M. & Sölkner, J. (2012) Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses. Bmc genomics, 13 (13:365), 1-13 doi::10.1186/1471-2164-13-365.
@article{article, author = {Sundstr\"{o}m, Elisabeth and Imsland, Freyja and Mikko, Sofia and Wade, Claire and Sigurdsson, Snaevar and Pielberg, Gerli R and Golovko, Anna and Curik, Ino and Seltenhammer, Monika H and S\"{o}lkner, Johann and Lindblad-Toh, Kerstin and Andersson, Leif}, year = {2012}, pages = {1-13}, DOI = {doi:10.1186/1471-2164-13-365}, keywords = {STX17, Melanoma, Hair greying, Copy number variation, Melanocytes}, journal = {Bmc genomics}, doi = {doi:10.1186/1471-2164-13-365}, volume = {13}, number = {13:365}, issn = {1471-2164}, title = {Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses}, keyword = {STX17, Melanoma, Hair greying, Copy number variation, Melanocytes} }
@article{article, author = {Sundstr\"{o}m, Elisabeth and Imsland, Freyja and Mikko, Sofia and Wade, Claire and Sigurdsson, Snaevar and Pielberg, Gerli R and Golovko, Anna and Curik, Ino and Seltenhammer, Monika H and S\"{o}lkner, Johann and Lindblad-Toh, Kerstin and Andersson, Leif}, year = {2012}, pages = {1-13}, DOI = {doi:10.1186/1471-2164-13-365}, keywords = {STX17, Melanoma, Hair greying, Copy number variation, Melanocytes}, journal = {Bmc genomics}, doi = {doi:10.1186/1471-2164-13-365}, volume = {13}, number = {13:365}, issn = {1471-2164}, title = {Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses}, keyword = {STX17, Melanoma, Hair greying, Copy number variation, Melanocytes} }

Časopis indeksira:


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


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