Arrieta-Bolaños E, Madrigal J A, Shaw B E
Anthony Nolan Research Institute, Royal Free Hospital, London, UK; Cancer Institute, University College London, Royal Free Campus, London, UK; Centro de Investigaciones en Hematología y Trastornos Afines (CIHATA), Universidad de Costa Rica, San José, Costa Rica.
Tissue Antigens. 2015 Jun;85(6):484-91. doi: 10.1111/tan.12555. Epub 2015 Mar 24.
Transforming growth factor β-1, encoded by the TGFB1 gene, is a cytokine that plays a central role in many physiologic and pathogenic processes with pleiotropic effects. Regulatory activity for this gene has been shown for 3.0 kb between positions -2665 and +423 from its translational start site. At least 17 TGFB1 regulatory region and exon 1 alleles have been defined on the basis of 18 polymorphic sites. Polymorphisms in TGFB1's regulatory region have been associated with differential levels of expression of this cytokine and to genetic risk in cancer and transplantation. In this report, we present 19 novel TGFB1 regulatory region and exon 1 alleles: p018-p036. Amplification of TGFB1's regulatory region was performed with an in-house protocol, and novel alleles were defined by either allele-specific amplification and/or molecular cloning of the amplicons, followed by sequencing in isolation. Three of these novel alleles (p018, p019, and p020) are shown to be formed by novel combinations of the aforementioned known polymorphic positions. Another 16 novel alleles are shown to carry additional known and unknown single-nucleotide polymorphisms. Polymorphism in TGFB1's regulatory region could have an impact on important processes, including embryogenesis, hematopoiesis, carcinogenesis, angiogenesis, fibrosis, immune responses, and transplantation, making its characterization necessary.
由TGFB1基因编码的转化生长因子β-1是一种细胞因子,在许多具有多效性的生理和致病过程中发挥核心作用。已表明该基因在其翻译起始位点上游-2665至+423位置之间3.0 kb的区域具有调控活性。基于18个多态性位点,已定义了至少17个TGFB1调控区和外显子1等位基因。TGFB1调控区的多态性与该细胞因子的不同表达水平以及癌症和移植中的遗传风险相关。在本报告中,我们呈现了19个新的TGFB1调控区和外显子1等位基因:p018 - p036。TGFB1调控区的扩增采用内部方案进行,新等位基因通过等位基因特异性扩增和/或扩增子的分子克隆来定义,随后单独进行测序。其中三个新等位基因(p018、p019和p020)显示为由上述已知多态性位点的新组合形成。另外16个新等位基因显示携带额外的已知和未知单核苷酸多态性。TGFB1调控区的多态性可能对包括胚胎发生、造血、致癌作用、血管生成、纤维化、免疫反应和移植在内的重要过程产生影响,因此有必要对其进行表征。