Molecular characterization of five Italian families with inherited severe factor XIII deficiency.

Castaman, G; Giacomelli, S H; Ivaskevicius, V; Schroeder, Verena; Kohler, Hans-Peter; Dragani, A; Biasioli, C; Oldenburg, J; Madeo, D; Rodeghiero, F (2008). Molecular characterization of five Italian families with inherited severe factor XIII deficiency. Haemophilia, 14(1), pp. 96-102. Wiley 10.1111/j.1365-2516.2007.01603.x

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Factor XIII (FXIII) deficiency is a very rare (1:2 000 000) severe autosomal recessive bleeding disorder, mostly due to mutations in the coagulation FXIII A-subunit gene. We have studied the molecular basis of FXIII deficiency in five unrelated Italian families. The coding region, intron-exon boundaries and 5'- and 3'-untranslated regions of the FXIII gene encoding the A subunit were amplified and directly sequenced. Candidate mutations were identified in all the patients. Three novel mutations occurred in three patients. These include a novel homozygous deletion of two base pairs (bp) in exon 14 (c.2002-2003 DelCT). This deletion causes a frameshift from Leu667 and the formation of a stop codon at amino acid position 681. The second patient presents a novel homozygous (c.2126 G>A) transition in exon 15, predicting a Ser708Asn in Barrel 2 domain. The third patient is compound heterozygote for two missense mutations, a previously reported Arg260His substitution, and a novel transition in exon 4 (c.560 C>T) predicting a Pro186Leu in the core domain. The remaining two patients have two previously reported mutations: a 4-bp homozygous deletion in exon 11 (c.1392-1395 Del AATT), previously reported to occur in the Vicenza Area, and a homozygous nonsense mutation in exon 8 (c.979 C>T) predicting an Arg326X in the core domain. The novel mutations occurred at amino acid residues highly conserved among different species (pig, monkey, mouse and dog) and were not detected in 110 normal alleles. Structural analysis shows that Pro186Leu mutation leads to the replacement of the rigid proline pyrrolidine ring by the larger and more flexible leucine side chain and Ser708Asn may probably disrupt the hydrogen bond with Ala291.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > Forschungsbereich Pavillon 52 > Forschungsgruppe Experimentelle Hämostase
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR)

UniBE Contributor:

Schröder, Verena

Subjects:

600 Technology > 610 Medicine & health

ISSN:

1365-2516

Publisher:

Wiley

Language:

English

Submitter:

Marla Rittiner

Date Deposited:

14 Jan 2020 12:37

Last Modified:

14 Jan 2020 12:37

Publisher DOI:

10.1111/j.1365-2516.2007.01603.x

PubMed ID:

18028394

BORIS DOI:

10.7892/boris.138278

URI:

https://boris.unibe.ch/id/eprint/138278

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