Pretražite po imenu i prezimenu autora, mentora, urednika, prevoditelja

Napredna pretraga

Pregled bibliografske jedinice broj: 218014

Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)


Zenker, Martin; Mayerle, Julia; Lerch, Markus M.; Tagariello, Andreas; Zerres, Klaus; Durie, Peter R.; Beier, Matthias; Hülskamp, Georg; Guzman, Celina; Rehder, Helga et al.
Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome) // Nature Genetics, 37 (2005), 12; 1345-1350 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 218014 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)

Autori
Zenker, Martin ; Mayerle, Julia ; Lerch, Markus M. ; Tagariello, Andreas ; Zerres, Klaus ; Durie, Peter R. ; Beier, Matthias ; Hülskamp, Georg ; Guzman, Celina ; Rehder, Helga ; Beemer, Frits A. ; Hame, Ben ; Vanlieferinghen, Philippe ; Gershoni-Baruch, Ruth ; Vieira, Marta W. ; Dumić, Miroslav ; Auslender, Ron ; Gil-da-Silva-Lopes, Vera L. ; Steinlicht, Simone ; Rauh, Manfred ; Shalev, Stavit A. ; Thiel, Christian ; Winterpacht, Andreas ; Kwon, Young Tae ; Varshavsky, Alexander ; Reis, André

Izvornik
Nature Genetics (1061-4036) 37 (2005), 12; 1345-1350

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

Ključne riječi
Johanson-Blizzard syndrome; pancreatic insufficiency; nasal wing aplasia

Sažetak
Johanson-Blizzard syndrome (JBS ; OMIM 243800) is an autosomal recessive disorder that includes congenital exocrine pancreatic insufficiency, multiple malformations, such as nasal wing aplasia, and frequent mental retardation1. We mapped the disease locus to chromosome 15q14-21.1, and identified mutations, mostly truncating ones, in the UBR1 gene in 12 unrelated JBS families. UBR1 encodes one of at least four functionally overlapping E3 ubiquitin ligases of the N-end rule pathway, a conserved proteolytic system whose substrates include proteins with destabilizing N-terminal residues2-5. Pancreas of JBS patients did not express UBR1, and exhibited intrauterine-onset destructive pancreatitis. We also show that UBR1– /– mice, whose previously reported phenotypes include reduced weight and behavioural abnormalities6, 7, have an exocrine pancreatic insufficiency, with impaired stimulus-secretion coupling and increased susceptibility to pancreatic injury. Our findings indicate that deficiency of UBR1 perturbs the pancreas’ acinar cells and other organs, presumably owing to metabolic stabilization of specific substrates of the N-end rule pathway.

Izvorni jezik
Engleski



POVEZANOST RADA


Projekti:
0108077

Ustanove:
Medicinski fakultet, Zagreb

Profili:

Avatar Url Miroslav Dumić (autor)


Citiraj ovu publikaciju:

Zenker, Martin; Mayerle, Julia; Lerch, Markus M.; Tagariello, Andreas; Zerres, Klaus; Durie, Peter R.; Beier, Matthias; Hülskamp, Georg; Guzman, Celina; Rehder, Helga et al.
Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome) // Nature Genetics, 37 (2005), 12; 1345-1350 (međunarodna recenzija, članak, znanstveni)
Zenker, M., Mayerle, J., Lerch, M., Tagariello, A., Zerres, K., Durie, P., Beier, M., Hülskamp, G., Guzman, C. & Rehder, H. (2005) Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome). Nature Genetics, 37 (12), 1345-1350.
@article{article, author = {Zenker, Martin and Mayerle, Julia and Lerch, Markus M. and Tagariello, Andreas and Zerres, Klaus and Durie, Peter R. and Beier, Matthias and H\"{u}lskamp, Georg and Guzman, Celina and Rehder, Helga and Beemer, Frits A. and Hame, Ben and Vanlieferinghen, Philippe and Gershoni-Baruch, Ruth and Vieira, Marta W. and Dumi\'{c}, Miroslav and Auslender, Ron and Gil-da-Silva-Lopes, Vera L. and Steinlicht, Simone and Rauh, Manfred and Shalev, Stavit A. and Thiel, Christian and Winterpacht, Andreas and Kwon, Young Tae and Varshavsky, Alexander and Reis, Andr\'{e}}, year = {2005}, pages = {1345-1350}, keywords = {Johanson-Blizzard syndrome, pancreatic insufficiency, nasal wing aplasia}, journal = {Nature Genetics}, volume = {37}, number = {12}, issn = {1061-4036}, title = {Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)}, keyword = {Johanson-Blizzard syndrome, pancreatic insufficiency, nasal wing aplasia} }
@article{article, author = {Zenker, Martin and Mayerle, Julia and Lerch, Markus M. and Tagariello, Andreas and Zerres, Klaus and Durie, Peter R. and Beier, Matthias and H\"{u}lskamp, Georg and Guzman, Celina and Rehder, Helga and Beemer, Frits A. and Hame, Ben and Vanlieferinghen, Philippe and Gershoni-Baruch, Ruth and Vieira, Marta W. and Dumi\'{c}, Miroslav and Auslender, Ron and Gil-da-Silva-Lopes, Vera L. and Steinlicht, Simone and Rauh, Manfred and Shalev, Stavit A. and Thiel, Christian and Winterpacht, Andreas and Kwon, Young Tae and Varshavsky, Alexander and Reis, Andr\'{e}}, year = {2005}, pages = {1345-1350}, keywords = {Johanson-Blizzard syndrome, pancreatic insufficiency, nasal wing aplasia}, journal = {Nature Genetics}, volume = {37}, number = {12}, issn = {1061-4036}, title = {Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)}, keyword = {Johanson-Blizzard syndrome, pancreatic insufficiency, nasal wing aplasia} }

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





Contrast
Increase Font
Decrease Font
Dyslexic Font