| Literature DB >> 25452492 |
Pamela A Harvey1, Christopher Wall2, Stephen W Luckey3, Stephen Langer1, Leslie A Leinwand4.
Abstract
Undergraduate science education curricula are traditionally composed of didactic instruction with a small number of laboratory courses that provide introductory training in research techniques. Research on learning methodologies suggests this model is relatively ineffective, whereas participation in independent research projects promotes enhanced knowledge acquisition and improves retention of students in science. However, availability of faculty mentors and limited departmental budgets prevent the majority of students from participating in research. A need therefore exists for this important component in undergraduate education in both small and large university settings. A course was designed to provide students with the opportunity to engage in a research project in a classroom setting. Importantly, the course collaborates with a sponsor's laboratory, producing a symbiotic relationship between the classroom and the laboratory and an evolving course curriculum. Students conduct a novel gene expression study, with their collective data being relevant to the ongoing research project in the sponsor's lab. The success of this course was assessed based on the quality of the data produced by the students, student perception data, student learning gains, and on whether the course promoted interest in and preparation for careers in science. In this paper, we describe the strategies and outcomes of this course, which represents a model for efficiently providing research opportunities to undergraduates.Entities:
Mesh:
Year: 2014 PMID: 25452492 PMCID: PMC4255356 DOI: 10.1187/cbe.14-05-0089
Source DB: PubMed Journal: CBE Life Sci Educ ISSN: 1931-7913 Impact factor: 3.325
Demographics of the 84 students enrolled between Spring 2009 and Fall 2013
| Percentage of students ( | |
|---|---|
| Male | 53.6 |
| Female | 46.4 |
| Ethnicity | |
| Underrepresented minoritiesa | 6.0 |
| Foreign exchange | 9.5 |
| Year | |
| Freshman | 7.1 |
| Sophomore | 3.6 |
| Junior | 29.8 |
| Senior | 40.5 |
| Fifth-year senior | 19.0 |
| Major | |
| MCDB | 79.8 |
| Biochemistry | 8.3 |
| Other | 11.9 |
aThis category includes African-American and Latino students.
Representative lecture topics from Fall 2009 to Fall 2013
| Lecture 1 | Course introduction, general chemistry review |
| Lecture 2 | Sponsor's lab member lecture 1: Overview of the python project |
| Lectures 3–6 | Primer design |
| Lecture 7 | Sponsor's lab member lecture 2: Gene candidate review |
| Lecture 8 | RNA isolation and spectrophotometry |
| Lecture 9 | cDNA synthesis |
| Lecture 10 | 10-min talk: review and demonstration |
| Lecture 11 | Cloning and enzyme restriction analysis |
| Lecture 12 | Pipetting accuracy and exercise review/demonstration |
| Lectures 13–15 | Introduction to qPCR |
| Lecture 16 | Biostatistics |
| Lecture 17 | Poster examples and demonstration of presentation |
Learning objectives and assessments of the Python Project
| Learning objective | Assessment |
|---|---|
| 1. Design experiments to measure gene expression in postprandial Burmese python tissues | Midterm examination, oral presentation, poster session, and research paper |
| 2. Perform experiments to validate all aspects of experimental design | In silico validation of primers in a related species, PCR validation of product size, and qPCR validation of single-product amplification |
| 3. Research background on the gene of choice using primary literature and develop a well-supported hypothesis | Review paper, oral presentation, poster session, and research paper |
| 4. Understand and be able to describe the rationale for each experiment and choice of gene | Poster session and research paper |
| 5. Develop proficiency in qPCR | qPCR experiments |
| 6. Present data effectively in a public poster presentation | Poster session |
Figure 1.Flowchart of experimental design. The course requires three major processes: primer design (gray boxes), validation of appropriate techniques (blue boxes), and measurement of gene expression (white boxes). Primers are designed using the assembled transcript for the gene of interest. In silico validation includes translation of the assembled transcript and verification of the intended product amplified by the primers. Primers are also tested in vitro using conventional PCR; the students evaluate whether a product of the correct size is amplified by using their primers. While primers are being synthesized, students begin pipetting exercises to demonstrate accurate pipetting skills before beginning qPCR. These exercises include production of standard curves using a protein assay and a highly expressed control gene using qPCR. The semester culminates with qPCR experiments to measure expression of students’ genes of interest, which requires both RNA isolation and cDNA synthesis.
Materials provided to students in the Python Projecta
| Common use laboratory equipment | Bench supplies for each student |
|---|---|
| Bio-Rad CFX96 Real-Time PCR | Tips: P10, P20, P200, |
a Each student is provided bench supplies for their use only as well as shared resources, including the larger equipment in the laboratory. All supplies, with the exception of disposables, are returned at the end of the semester.
Techniques learned by each student in the Python Project and validation methods required to proceed to the next experimental step
| Technique | Validation | Criteria for success |
|---|---|---|
| RNA isolation | 1. Spectrophotometry | A260/280 greater than 1.8 |
| 2. Denaturing gel electrophoresis | Two clear bands representing 18S and 28S rRNA | |
| Primer design | 1. Amino acid translation of assembled transcript | One reading frame with no stop codons introduced |
| 2. In silico Protein BLAST | Correct protein returned in a closely related species | |
| 3. Conventional PCR | Correctly sized product amplified | |
| 4. qPCR | Single melt curve for the amplified product | |
| cDNA synthesis | Conventional PCR | Amplification of a housekeeping gene in all samples |
| Measurement of gene expression | Multiple qPCR experiments | Results must be repeatable |
Figure 2.Pre- and posttest student self-evaluation summary. The students evaluated their confidence in seven laboratory skills (questions 1–7) and 10 molecular biology techniques (questions 8–17). (For a list of the questions, see Figure S1.) An unannounced pretest was administered on the first day of class, and an identical survey was administered on the last day. Responses were recorded for three semesters (n = 27 students). Results are reported for the average gains in each area for all students (white bars) and for individual students (gray bars). Error bars represent SEM.
Pre- and posttest molecular biology knowledge resultsa
| Pretest average score | Posttest average score | Percent increase in score | |
|---|---|---|---|
| Gel electrophoresis | 78.6 | 92.8 | 14.2 |
| DNA structure | 80.7 | 85.7 | 5 |
| Reverse complement DNA sequence | 85.7 | 100 | 14.3 |
| Parameters affecting annealing temperature | 14.3 | 78.6 | 64.3 |
| Properties of | 64.3 | 92.8 | 28.5 |
| Spectrophotometry | 57.1 | 100 | 42.9 |
| Define “conserved sequence” | 71.4 | 92.8 | 21.4 |
a See also Figure S2.
Figure 3.Student opinions of the Python Project. An annonymous survey was administered through SurveyMonkey to students who had completed the course between 2009 and 2013. The percentage of responding students in each category is indicated below the circle graphs.
Figure 4.Intended education plans at the beginning (Entry Survey) and end (Exit Survey) of students participating in the Python Project between 2010 and 2013.
Figure 5.Effect of the Python Project on students’ career and education choices.