Parmo-Folloni Fernando, Nunes Kelly, Lepienski Luís M, Mikami Liya R, Souza Ricardo L R, Tsuneto Luiza T, Petzl-Erler Maria Luiza, Chautard-Freire-Maia Eleidi A
Department of Genetics, Federal University of Paraná, Curitiba, PR, Brazil.
Chem Biol Interact. 2008 Sep 25;175(1-3):135-7. doi: 10.1016/j.cbi.2008.04.038. Epub 2008 May 4.
The genetic variation of human butyrylcholinesterase is associated with the majority of prolonged cases of apnea in patients submitted to the muscle relaxant succinylcholine. The present study reports two new mutations of the BCHE gene in 346 Euro-Brazilians: IVS3-14T>C found in five heterozygotes (allele frequency: 0.72+/-0.32%) and L574fsX576 found in one heterozygote (allele frequency: 0.14+/-0.14%). These two variants were not found in 85 Guarani Amerindians. It is not expected that the IVS3-14T>C mutation may interfere in the splicing process and that the mutation found in exon 4 (L574fsX576) may disturb BChE tetramerization and activity.
人类丁酰胆碱酯酶的基因变异与接受肌肉松弛剂琥珀酰胆碱治疗的患者中大多数呼吸暂停延长病例相关。本研究报告了346名欧洲裔巴西人中BCHE基因的两个新突变:IVS3-14T>C在5名杂合子中发现(等位基因频率:0.72±0.32%),L574fsX576在1名杂合子中发现(等位基因频率:0.14±0.14%)。在85名瓜拉尼美洲印第安人中未发现这两种变异。预计IVS3-14T>C突变不会干扰剪接过程,外显子4中发现的突变(L574fsX576)不会干扰丁酰胆碱酯酶的四聚化和活性。