TY - JOUR
T1 - A novel Asn344 deletion in the core domain of coagulation factor XIII a subunit
T2 - Its effects on protein structure and function
AU - Kangsadalampai, Sasichai
AU - Chelvanayagam, Gareth
AU - Baker, Rohan T.
AU - Yenchitsomanus, Pa Thai
AU - Pung-amritt, Parichat
AU - Mahasandana, Chularatana
AU - Board, Philip G.
PY - 1998/7/15
Y1 - 1998/7/15
N2 - In this study a previously undescribed 3 bp deletion, AAT1030- 1032, in the factor XIII A subunit gene, has been detected in a Thai patient. The inframe deletion results in the translation of a factor XIII A subunit that lacks Asn344. This is the first inframe deletion to be identified in the factor XIII A subunit gene because six previously reported deletions have all caused frameshifts. The deletion has been introduced into a factor XIII A subunit cDNA and the deleted polypeptide expressed in yeast. The mRNA encoding the mutant enzyme appears to have normal stability but the translated protein is subject to premature degradation. In addition, the mutated enzyme exhibited very little transglutaminase activity compared with the wild-type enzyme. Structural modeling of the deleted enzyme suggests that the absence of Asn344 would have a potent impact on the catalytic activity by reorienting the residues associated with the catalytic center. Thus, the Asn344 deletion strongly confirms the significance of the residues surrounding the catalytic center of the factor XIII A subunit.
AB - In this study a previously undescribed 3 bp deletion, AAT1030- 1032, in the factor XIII A subunit gene, has been detected in a Thai patient. The inframe deletion results in the translation of a factor XIII A subunit that lacks Asn344. This is the first inframe deletion to be identified in the factor XIII A subunit gene because six previously reported deletions have all caused frameshifts. The deletion has been introduced into a factor XIII A subunit cDNA and the deleted polypeptide expressed in yeast. The mRNA encoding the mutant enzyme appears to have normal stability but the translated protein is subject to premature degradation. In addition, the mutated enzyme exhibited very little transglutaminase activity compared with the wild-type enzyme. Structural modeling of the deleted enzyme suggests that the absence of Asn344 would have a potent impact on the catalytic activity by reorienting the residues associated with the catalytic center. Thus, the Asn344 deletion strongly confirms the significance of the residues surrounding the catalytic center of the factor XIII A subunit.
UR - http://www.scopus.com/inward/record.url?scp=0032528345&partnerID=8YFLogxK
U2 - 10.1182/blood.v92.2.481
DO - 10.1182/blood.v92.2.481
M3 - Article
SN - 0006-4971
VL - 92
SP - 481
EP - 487
JO - Blood
JF - Blood
IS - 2
ER -