首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Drosophila transposon insertions as unknowns for structured inquiry recombination mapping exercises in an undergraduate genetics course.
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Drosophila transposon insertions as unknowns for structured inquiry recombination mapping exercises in an undergraduate genetics course.

机译:果蝇转座子插入作为未知物,用于在大学遗传学课程中进行结构化查询重组作图。

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Structured inquiry approaches, in which students receive a Drosophila strain of unknown genotype to analyze and map the constituent mutations, are a common feature of many genetics teaching laboratories. The required crosses frustrate many students because they are aware that they are participating in a fundamentally trivial exercise, as the map locations of the genes are already established and have been recalculated thousands of times by generations of students. We modified the traditional structured inquiry approach to include a novel research experience for the students in our undergraduate genetics laboratories. Students conducted crosses with Drosophila strains carrying P[lacW] transposon insertions in genes without documented recombination map positions, representing a large number of unique, but equivalent genetic unknowns. Using the eye color phenotypes associated with the inserts as visible markers, it is straightforward to calculate recombination map positions for the interrupted loci. Collectively, our students mapped 95 genetic loci on chromosomes 2 and 3. In most cases, the calculated 95% confidence interval for meiotic map location overlapped with the predicted map position based on cytology. The research experience evoked positive student responses and helped students better understand the nature of scientific research for little additional cost or instructor effort.
机译:结构化探究方法是许多遗传学教学实验室的共同特征,在这种方法中,学生会收到一个未知基因型的果蝇菌株,以分析和绘制组成突变。必需的杂交使许多学生感到沮丧,因为他们知道他们正在参加一项从根本上讲是微不足道的练习,因为基因的图谱位置已经确定,几代学生已经对其进行了数千次重新计算。我们对传统的结构化探究方法进行了修改,为本科遗传学实验室的学生提供了新颖的研究经验。学生与果蝇菌株杂交,该菌株在基因中携带有P [lacW]转座子插入,而没有记录重组图的位置,代表了大量独特但等效的遗传未知数。使用与插入物相关的眼睛颜色表型作为可见标记,可以轻松计算出中断基因座的重组图位置。总的来说,我们的学生在2号和3号染色体上绘制了95个遗传基因座。在大多数情况下,减数分裂图位置的计算出的95%置信区间与基于细胞学的预测图位重叠。研究经验引起了学生的积极响应,并帮助学生以很少的额外成本或老师的努力就能更好地了解科学研究的性质。

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