Robertson Amber L, Phillips Allison R
Department of Horticulture and Laboratory of Genetics, University of Wisconsin-Madison, Madison, WI 53706, USA.
CBE Life Sci Educ. 2008 Spring;7(1):89-95. doi: 10.1187/cbe.07-07-0051.
Polymerase chain reaction (PCR) is a conceptually difficult technique that embodies many fundamental biological processes. Traditionally, students have struggled to analyze PCR results due to an incomplete understanding of the biological concepts (theory) of DNA replication and strand complementarity. Here we describe the design of a novel research-oriented exercise that prepares students to design DNA primers for PCR. Our exercise design includes broad and specific learning goals and assessments of student performance and perceptions. We developed this interactive Primer Design Exercise using the principles of scientific teaching to enhance student understanding of the theory behind PCR and provide practice in designing PCR primers to amplify DNA. In the end, the students were more poised to troubleshoot problems that arose in real experiments using PCR. In addition, students had the opportunity to utilize several bioinformatics tools to gain an increased understanding of primer quality, directionality, and specificity. In the course of this study many misconceptions about DNA replication during PCR and the need for primer specificity were identified and addressed. Students were receptive to the new materials and the majority achieved the learning goals.
聚合酶链反应(PCR)是一项在概念上较难的技术,它体现了许多基本的生物学过程。传统上,由于对DNA复制和链互补性的生物学概念(理论)理解不完整,学生们在分析PCR结果时遇到了困难。在此,我们描述了一项新颖的以研究为导向的练习设计,该练习能让学生为PCR设计DNA引物做好准备。我们的练习设计包括广泛和具体的学习目标以及对学生表现和认知的评估。我们运用科学教学原理开发了这个交互式引物设计练习,以增强学生对PCR背后理论的理解,并提供设计PCR引物以扩增DNA的实践机会。最后,学生们更有能力解决在使用PCR的实际实验中出现的问题。此外,学生有机会使用多种生物信息学工具,以加深对引物质量、方向性和特异性的理解。在这项研究过程中,发现并解决了许多关于PCR过程中DNA复制以及引物特异性需求的误解。学生们接受了新材料,大多数人实现了学习目标。