Noh S-J, Lee Y T, Byrnes C, Miller J L
Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH), 31 Center Drive, Bethesda, Building 10, Room 9N311, MD 20892, USA.
Transfus Clin Biol. 2010 Sep;17(3):120-5. doi: 10.1016/j.tracli.2010.06.010. Epub 2010 Aug 3.
Over the last two decades, red cell biologists witnessed a vast expansion of genetic-based information pertaining to blood group antigens and their carrier molecules. Genetic progress has led to a better comprehension of the associated antigens. To assist with studies concerning the integrated regulation and function of blood groups, transcript levels for each of the 36 associated genes were studied. Profiles using mRNA from directly sampled reticulocytes and cultured primary erythroblasts are summarized in this report. Transcriptome profiles suggest a highly regulated pattern of blood group gene expression during erythroid differentiation and ontogeny. Approximately one-third of the blood group carrier genes are transcribed in an erythroid-specific fashion. Low-level and indistinct expression was noted for most of the carbohydrate-associated genes. Methods are now being developed to further explore and manipulate expression of the blood group genes at all stages of human erythropoiesis.
在过去二十年中,红细胞生物学家见证了与血型抗原及其载体分子相关的基于基因的信息大量增加。遗传学进展使人们对相关抗原的理解更加深入。为了协助有关血型综合调控和功能的研究,对36个相关基因中每个基因的转录水平进行了研究。本报告总结了使用直接采集的网织红细胞和培养的原代成红细胞的mRNA的分析结果。转录组分析结果表明,在红细胞分化和个体发育过程中,血型基因表达呈现高度调控的模式。大约三分之一的血型载体基因以红细胞特异性方式转录。大多数与碳水化合物相关的基因表达水平较低且不明显。目前正在开发相关方法,以进一步探索和操纵人类红细胞生成各个阶段血型基因的表达。