Cargando…
Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2
Type 3 Von Willebrand disease is an autosomal recessive disease caused by the virtual absence of the von Willebrand factor (VWF). A rare 253 kb gene deletion on chromosome 12, identified only in Italian and German families, involves both the VWF gene and the N-terminus of the neighbouring TMEM16B/AN...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4312080/ https://www.ncbi.nlm.nih.gov/pubmed/25635880 http://dx.doi.org/10.1371/journal.pone.0116483 |
_version_ | 1782355092766195712 |
---|---|
author | Cenedese, Valentina Mezzavilla, Massimo Morgan, Anna Marino, Renato Ettorre, Cosimo Pietro Margaglione, Maurizio Gasparini, Paolo Menini, Anna |
author_facet | Cenedese, Valentina Mezzavilla, Massimo Morgan, Anna Marino, Renato Ettorre, Cosimo Pietro Margaglione, Maurizio Gasparini, Paolo Menini, Anna |
author_sort | Cenedese, Valentina |
collection | PubMed |
description | Type 3 Von Willebrand disease is an autosomal recessive disease caused by the virtual absence of the von Willebrand factor (VWF). A rare 253 kb gene deletion on chromosome 12, identified only in Italian and German families, involves both the VWF gene and the N-terminus of the neighbouring TMEM16B/ANO2 gene, a member of the family named transmembrane 16 (TMEM16) or anoctamin (ANO). TMEM16B is a calcium-activated chloride channel expressed in the olfactory epithelium. As a patient homozygous for the 253 kb deletion has been reported to have an olfactory impairment possibly related to the partial deletion of TMEM16B, we assessed the olfactory function in other patients using the University of Pennsylvania Smell Identification Test (UPSIT). The average UPSIT score of 4 homozygous patients was significantly lower than that of 5 healthy subjects with similar sex, age and education. However, 4 other members of the same family, 3 heterozygous for the deletion and 1 wild type, had a slightly reduced olfactory function indicating that socio-cultural or other factors were likely to be responsible for the observed difference. These results show that the ability to identify odorants of the homozygous patients for the deletion was not significantly different from that of the other members of the family, showing that the 253 kb deletion does not affect the olfactory performance. As other genes may compensate for the lack of TMEM16B, we identified some predicted functional partners from in silico studies of the protein-protein network of TMEM16B. Calculation of diversity for the corresponding genes for individuals of the 1000 Genomes Project showed that TMEM16B has the highest level of diversity among all genes of the network, indicating that TMEM16B may not be under purifying selection and suggesting that other genes in the network could compensate for its function for olfactory ability. |
format | Online Article Text |
id | pubmed-4312080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43120802015-02-13 Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2 Cenedese, Valentina Mezzavilla, Massimo Morgan, Anna Marino, Renato Ettorre, Cosimo Pietro Margaglione, Maurizio Gasparini, Paolo Menini, Anna PLoS One Research Article Type 3 Von Willebrand disease is an autosomal recessive disease caused by the virtual absence of the von Willebrand factor (VWF). A rare 253 kb gene deletion on chromosome 12, identified only in Italian and German families, involves both the VWF gene and the N-terminus of the neighbouring TMEM16B/ANO2 gene, a member of the family named transmembrane 16 (TMEM16) or anoctamin (ANO). TMEM16B is a calcium-activated chloride channel expressed in the olfactory epithelium. As a patient homozygous for the 253 kb deletion has been reported to have an olfactory impairment possibly related to the partial deletion of TMEM16B, we assessed the olfactory function in other patients using the University of Pennsylvania Smell Identification Test (UPSIT). The average UPSIT score of 4 homozygous patients was significantly lower than that of 5 healthy subjects with similar sex, age and education. However, 4 other members of the same family, 3 heterozygous for the deletion and 1 wild type, had a slightly reduced olfactory function indicating that socio-cultural or other factors were likely to be responsible for the observed difference. These results show that the ability to identify odorants of the homozygous patients for the deletion was not significantly different from that of the other members of the family, showing that the 253 kb deletion does not affect the olfactory performance. As other genes may compensate for the lack of TMEM16B, we identified some predicted functional partners from in silico studies of the protein-protein network of TMEM16B. Calculation of diversity for the corresponding genes for individuals of the 1000 Genomes Project showed that TMEM16B has the highest level of diversity among all genes of the network, indicating that TMEM16B may not be under purifying selection and suggesting that other genes in the network could compensate for its function for olfactory ability. Public Library of Science 2015-01-30 /pmc/articles/PMC4312080/ /pubmed/25635880 http://dx.doi.org/10.1371/journal.pone.0116483 Text en © 2015 Cenedese et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Cenedese, Valentina Mezzavilla, Massimo Morgan, Anna Marino, Renato Ettorre, Cosimo Pietro Margaglione, Maurizio Gasparini, Paolo Menini, Anna Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2 |
title | Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2
|
title_full | Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2
|
title_fullStr | Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2
|
title_full_unstemmed | Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2
|
title_short | Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2
|
title_sort | assessment of the olfactory function in italian patients with type 3 von willebrand disease caused by a homozygous 253 kb deletion involving vwf and tmem16b/ano2 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4312080/ https://www.ncbi.nlm.nih.gov/pubmed/25635880 http://dx.doi.org/10.1371/journal.pone.0116483 |
work_keys_str_mv | AT cenedesevalentina assessmentoftheolfactoryfunctioninitalianpatientswithtype3vonwillebranddiseasecausedbyahomozygous253kbdeletioninvolvingvwfandtmem16bano2 AT mezzavillamassimo assessmentoftheolfactoryfunctioninitalianpatientswithtype3vonwillebranddiseasecausedbyahomozygous253kbdeletioninvolvingvwfandtmem16bano2 AT morgananna assessmentoftheolfactoryfunctioninitalianpatientswithtype3vonwillebranddiseasecausedbyahomozygous253kbdeletioninvolvingvwfandtmem16bano2 AT marinorenato assessmentoftheolfactoryfunctioninitalianpatientswithtype3vonwillebranddiseasecausedbyahomozygous253kbdeletioninvolvingvwfandtmem16bano2 AT ettorrecosimopietro assessmentoftheolfactoryfunctioninitalianpatientswithtype3vonwillebranddiseasecausedbyahomozygous253kbdeletioninvolvingvwfandtmem16bano2 AT margaglionemaurizio assessmentoftheolfactoryfunctioninitalianpatientswithtype3vonwillebranddiseasecausedbyahomozygous253kbdeletioninvolvingvwfandtmem16bano2 AT gasparinipaolo assessmentoftheolfactoryfunctioninitalianpatientswithtype3vonwillebranddiseasecausedbyahomozygous253kbdeletioninvolvingvwfandtmem16bano2 AT meninianna assessmentoftheolfactoryfunctioninitalianpatientswithtype3vonwillebranddiseasecausedbyahomozygous253kbdeletioninvolvingvwfandtmem16bano2 |