Pitfalls of X‐chromosome inactivation testing in females with Fabry disease. Issue 7 (26th March 2022)
- Record Type:
- Journal Article
- Title:
- Pitfalls of X‐chromosome inactivation testing in females with Fabry disease. Issue 7 (26th March 2022)
- Main Title:
- Pitfalls of X‐chromosome inactivation testing in females with Fabry disease
- Authors:
- Řeboun, Martin
Sikora, Jakub
Magner, Martin
Wiederlechnerová, Helena
Černá, Alena
Poupětová, Helena
Štorkánova, Gabriela
Mušálková, Dita
Dostálová, Gabriela
Goláň, Lubor
Linhart, Aleš
Dvořáková, Lenka - Abstract:
- Abstract: Fabry disease (FD) is an X‐linked lysosomal storage disorder caused by mutations in the GLA gene encoding alpha‐galactosidase A (AGAL). The impact of X‐chromosome inactivation (XCI) on the phenotype of female FD patients remains unclear. In this study we aimed to determine pitfalls of XCI testing in a cohort of 35 female FD patients. XCI was assessed by two methylation‐based and two allele‐specific expression assays. The results correlated, although some variance among the four assays was observed. GLA transcript analyses identified crossing‐over in three patients and detected mRNA instability in three out of four analyzed null alleles. AGAL activity correlated with XCI pattern and was not influenced by the mutation type or by reduced mRNA stability. Therefore, AGAL activity may help to detect crossing‐over in patients with unstable GLA alleles. Tissue‐specific XCI patterns in six patients, and age‐related changes in two patients were observed. To avoid misinterpretation of XCI results in female FD patients we show that (i) a combination of several XCI assays generates more reliable results and minimizes possible biases; (ii) correlating XCI to GLA expression and AGAL activity facilitates identification of cross‐over events; (iii) age‐ and tissue‐related XCI specificities of XCI patterning should be considered.
- Is Part Of:
- American journal of medical genetics. Volume 188:Issue 7(2022)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 188:Issue 7(2022)
- Issue Display:
- Volume 188, Issue 7 (2022)
- Year:
- 2022
- Volume:
- 188
- Issue:
- 7
- Issue Sort Value:
- 2022-0188-0007-0000
- Page Start:
- 1979
- Page End:
- 1989
- Publication Date:
- 2022-03-26
- Subjects:
- alpha‐galactosidase A activity -- Fabry disease heterozygotes -- GLA transcript expression -- X chromosome inactivation assay
Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.62728 ↗
- Languages:
- English
- ISSNs:
- 1552-4825
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22090.xml