論文 - 詳細
| RRC ID | 64278 |
|---|---|
| 著者 | Maruyama K, Kokame K. |
| タイトル | Carrier frequencies of antithrombin, protein C, and protein S deficiency variants estimated using a public database and expression experiments. |
| ジャーナル | Res Pract Thromb Haemost |
| Abstract |
Background:Genetic deficiencies of antithrombin (AT), protein C (PC), and protein S (PS) are risk factors for venous thromboembolism. In the general population, the prevalence of heterozygous deficiency of AT, PC, and PS are reported as approximately 0.02%-0.2%, 0.2%-0.4%, and 0.03%-0.5%, respectively. The Exome Aggregation Consortium (ExAC) provides a public database containing reference data for over 60 000 exomes. Objective:This study aimed to determine the frequency of AT, PC, and PS deficiencies using the ExAC database and transient expression experiments. Methods:In total, 133, 157, and 221 variants of SERPIN1 (encoding AT), PROC (PC), and PROS1 (PS), respectively, were registered as missense and putative loss-of-function variants in the ExAC database. Variants with relatively high allele frequencies were selected and randomly sampled. Recombinant proteins were expressed in human embryo kidney 293 cells and their secretion and anticoagulant activities examined. Results and Conclusion:We assessed 9 AT, 4 PC, and 14 PS variants with relatively high allele frequencies and randomly sampled 12 AT, 15 PC, and 19 PS missense variants. All 21 AT variants showed normal or mildly reduced secretion, and 6 showed reduced total activity (specific activity × antigen level). Of the 19 PC variants, 11 showed impaired total activity. All 33 PS variants showed normal or mildly reduced secretion, and 4 showed reduced total activity. Based on allele frequencies in the ExAC database, we calculated the frequencies of AT, PC, and PS genetic deficiency as 0.36%, 0.63%, and 0.39%, respectively. |
| 巻・号 | 5(1) |
| ページ | 179-186 |
| 公開日 | 2021-1-1 |
| DOI | 10.1002/rth2.12456 |
| PII | RTH212456 |
| PMID | 33537542 |
| PMC | PMC7845069 |
| リソース情報 | |
| 遺伝子材料 | Genome Network Project Human cDNA Clone IRAK050H04 (HGX020172) |