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首页> 外文期刊>Advances in physiology education >'Sickle cell anemia: tracking down a mutation': an interactive learning laboratory that communicates basic principles of genetics and cellular biology
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'Sickle cell anemia: tracking down a mutation': an interactive learning laboratory that communicates basic principles of genetics and cellular biology

机译:“镰状细胞性贫血:追踪突变”:一个交流学习实验室,传达遗传学和细胞生物学的基本原理

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摘要

"Sickle cell anemia: tracking down a mutation" is a full-day, inquiry-based, biology experience for high school students enrolled in genetics or advanced biology courses. In the experience, students use restriction endonuclease digestion, cellulose acetate gel electrophoresis, and microscopy to discover which of three putative patients have the sickle cell genotype/phenotype using DNA and blood samples from wild-type and transgenic mice that carry a sickle cell mutation. The inquiry-based, problem-solving approach facilitates the students' understanding of the basic concepts of genetics and cellular and molecular biology and provides experience with contemporary tools of biotechnology. It also leads to students' appreciation of the causes and consequences of this genetic disease, which is relatively common in individuals of African descent, and increases their understanding of the first principles of genetics. This protocol provides optimal learning when led by well-trained facilitators (including the classroom teacher) and carried out in small groups (6:1 student-to-teacher ratio). This high-quality experience can be offered to a large number of students at a relatively low cost, and it is especially effective in collaboration with a local science museum and/or university. Over the past 15 yr, >12,000 students have completed this inquiry-based learning experience and demonstrated a consistent, substantial increase in their understanding of the disease and genetics in general.
机译:“镰状细胞性贫血:追踪突变”是针对遗传学或高级生物学课程的高中生的全日制,基于询问的生物学经验。在经验中,学生使用限制性核酸内切酶消化,醋酸纤维素凝胶电泳和显微镜检查法,利用来自带有镰状细胞突变的野生型和转基因小鼠的DNA和血液样本,发现三名推定的患者中哪些具有镰状细胞基因型/表型。以探究为基础,解决问题的方法有助于学生理解遗传学,细胞和分子生物学的基本概念,并提供使用现代生物技术工具的经验。它也使学生认识到这种遗传病的原因和后果,这种遗传病在非洲人后裔中相对普遍,并增加了他们对遗传学基本原理的理解。在训练有素的辅导员(包括课堂老师)的带领下,以小组形式(6:1的学生与老师的比例)进行操作时,此协议可提供最佳的学习效果。可以以相对较低的成本向大量学生提供这种高质量的体验,与当地的科学博物馆和/或大学合作特别有效。在过去的15年中,超过12,000名学生已经完成了这种基于探究的学习经验,并显示出他们对疾病和遗传学总体上的理解持续不断地大量增加。

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