Digital repository of Slovenian research organisations

Show document
A+ | A- | SLO | ENG

Title:SERPING1 variants and C1-INH biological function : a close relationship with C1-INH-HAE
Authors:ID Drouet, Christian (Author)
ID López Lera, Alberto (Author)
ID Ghannam, Arije (Author)
ID López-Trascasa, Margarita (Author)
ID Cichon, Sven (Author)
ID Ponard, Denise (Author)
ID Parsopoulou, Faidra (Author)
ID Grombirikova, Hana (Author)
ID Freiberger, Tomas (Author)
ID Rijavec, Matija, Klinika Golnik, Biotehniška fakulteta UL (Author)
ID Lopes Veronez, Camila (Author)
ID Pesquero, João Bosco (Author)
ID Germenis, Anastasios E. (Author)
Files:.docx DOCX - Presentation file, download (26,80 KB)
MD5: AD9A98F30A12155544BD5EA76EF83F5B
 
.pdf PDF - Presentation file, download (2,51 MB)
MD5: 1EC42A4C79F75680BD123AD1204A8624
 
Language:English
Typology:1.02 - Review Article
Organization:Logo UKPBAG - University Clinic of Respiratory and Allergic Diseases Golnik
Abstract:Hereditary angioedema with C1 Inhibitor deficiency (C1-INH-HAE) is caused by a constellation of variants of the SERPING1 gene (n = 809; 1,494 pedigrees), accounting for 86.8% of HAE families, showing a pronounced mutagenic liability of SERPING1 and pertaining to 5.6% de novo variants. C1-INH is the major control serpin of the kallikrein–kinin system (KKS). In addition, C1-INH controls complement C1 and plasminogen activation, both systems contributing to inflammation. Recognizing the failed control of C1s protease or KKS provides the diagnosis of C1-INH-HAE. SERPING1 variants usually behave in an autosomal-dominant character with an incomplete penetrance and a low prevalence. A great majority of variants (809/893; 90.5%) that were introduced into online database have been considered as pathogenic/likely pathogenic. Haploinsufficiency is a common feature in C1-INH-HAE where a dominant-negative variant product impacts the wild-type allele and renders it inactive. Small (36.2%) and large (8.3%) deletions/duplications are common, with exon 4 as the most affected one. Point substitutions with missense variants (32.2%) are of interest for the serpin structure–function relationship. Canonical splice sites can be affected by variants within introns and exons also (14.3%). For noncanonical sequences, exon skipping has been confirmed by splicing analyses of patients' blood-derived RNAs (n = 25). Exonic variants (n = 6) can affect exon splicing. Rare deep-intron variants (n = 6), putatively acting as pseudo-exon activating mutations, have been characterized as pathogenic. Some variants have been characterized as benign/likely benign/of uncertain significance (n = 74). This category includes some homozygous (n = 10) or compound heterozygous variants (n = 11). They are presenting with minor allele frequency (MAF) below 0.00002 (i.e., lower than C1-INH-HAE frequency), and may be quantitatively unable to cause haploinsufficiency. Rare benign variants could contribute as disease modifiers. Gonadal mosaicism in C1-INH-HAE is rare and must be distinguished from a de novo variant. Situations with paternal or maternal disomy have been recorded (n = 3). Genotypes must be interpreted with biological investigation fitting with C1-INH expression and typing. Any SERPING1 variant reminiscent of the dysfunctional phenotype of serpin with multimerization or latency should be identified as serpinopathy.
Keywords:Hereditary angioedemas -- genetics -- diagnosis, genetic variation, serpins, SERPING1 gene, C1-INH, C1-INH-HAE, C1 inhibitor, serpinopathy
Year of publishing:2022
Publication status in journal:In print
Article version:Publisher's version of article
Publisher:Frontiers
Number of pages:str. 1-17
Numbering:Vol. 3
Source:Švica
UDC:575
ISSN on article:2673-6101
DOI:10.3389/falgy.2022.835503 New window
COBISS.SI-ID:103075331 New window
Copyright:© 2022 Drouet, López-Lera, Ghannam, López-Trascasa, Cichon, Ponard, Parsopoulou, Grombirikova, Freiberger, Rijavec, Veronez, Pesquero and Germenis
Note:Soavtor iz Slovenije: Matija Rijavec; Nasl. z nasl. zaslona; Opis vira z dne 1. 4. 2022;
Publication date in DiRROS:06.04.2022
Views:182
Downloads:142
Metadata:XML RDF-CHPDL DC-XML DC-RDF
:
  
Share:AddThis
AddThis uses cookies that require your consent. Edit consent...

Hover the mouse pointer over a document title to show the abstract or click on the title to get all document metadata.

Record is a part of a journal

Title:Frontiers in allergy
Shortened title:Front. allergy
Publisher:Frontiers Media
ISSN:2673-6101
COBISS.SI-ID:59156227 New window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:31.03.2022

Secondary language

Language:Undetermined
Keywords:hereditarni angioedemi -- genetika -- diagnostika, genetska raznolikost, serpini, gen SERPING1, C1-INH, C1-INH-HAE, zaviralec C1, serpinopatija


Back