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Your responsibilities and mine
Instructor: Dr. Bonnie K. Baxter, bkbaxter@lclark.edu, x7653
Class Time & Place: MWF 8:00 am to 9:00 am, Thaxter 2
Office Hours: T.B.A.
Textbook: Molecular Cell Biology, by Lodish et al. 4th edition. W.H. Freeman & Company (this is also the textbook for Biology 361: Cell Biology).
Molecular Biology is about investigating how genotype becomes phenotype. Given a certain set of genetic instructions in its DNA, how does a cell read and interpret those instructions to go about its day-to-day activities? How does it adapt these readings and interpretations to different circumstances? How does it "know," for example, when it is time to move, when to eat, when to "sleep," and when to divide? In a multicellular organism, how do cells with the same set of instructions end up with such different fates and roles? How does a cone cell in your retina come to be so different from a muscle cell or a white blood cell?
The student of molecular biology will notice several underlying themes that are characteristic of this field:
1) Reductionism. Molecular Biology is a field of study that seeks to understand the nature of life at the level of molecules. The discipline is built upon the premise that we can understand complex biological phenomena by taking them apart and reconstructing the process in a test tube from its essential components. This reductionist approach to science has been enormously successful and the rate of growth of new information in this field of study has been explosive. The reductionist approach has led molecular biologists to appreciate
2) The unity of life. When approached at the level of molecules, all of life appears remarkably similar. All cells use DNA as their genetic material. With a few minor exceptions, all use exactly the same system for encoding protein sequences within that DNA, and the same general mechanisms for copying, transcribing, and translating that code. And as we will see in this course, there are relatively few types of control mechanisms for gene expression&emdash;the manifestation of genotype as phenotype. It is very often the case, for instance, that a mechanism discovered in a bacterial cell will turn out to be common in many other cell types, including human cells. The fact that particular discoveries are very often generalizable to other systems is one of the things that has led to
3) Extremely rapid change. James Watson and Francis Crick published the molecular structure of DNA in 1953. Today, less than 50 years later, the human genome project is on the verge of completing the sequence of the entire human genome (about 3 billion base pairs in all). It is now possible (and even straightforward) to look up the sequence of one of the 100,000 or so human genes on the internet and to design and carry out a strategy to "clone" that gene and introduce it into another organism. (We will be doing something very similar to this in the Bio312 lab, in fact.) Changes and rearrangements of DNA can be introduced almost at will, and their effects determined in cultured cells. The use of these technologies and others like them have led to a field in which our understanding of basic molecular processes is revised and updated on an annual, monthly, or even weekly basis. It has also led to a society in which our ability to do things in biotechnology has far outpaced our thinking about the implications of what we do.
As I see it, a science course has three quite different aspects: content, process, and context. The most straightforward thing to teach and learn is generally the content. What is our current understanding of how things work? In this case, what is DNA, how is it structured, and how its instructions interpreted? What have scientists learned about how genotype becomes phenotype? This is the sort of information that is conveyed effectively by textbooks and lectures. It is essential to build a solid foundation of understanding of this sort of material, because progress in science rests upon these foundations.
But of course science is not a static collection of "facts," but a process. Science as process relies on a solid understanding of what has gone before, but also on a willingness to expand and challenge current thinking. Learning to understand the process of science requires experience with experimental design, data analysis, and creative model building. Doing science requires thinking both inside and outside of the "box." Doing science requires skills like critical analysis, creativity, curiosity, and collaboration. These skills are learned most effectively in discussions, collaborations, and laboratory work.
Finally, science is a human activity that occurs in a social context. In molecular biology, this interface is apparent on a weekly or daily basis in the news media and in political events. Technologies such as genetic testing, genetic engineering, cloning, and molecular drug design all potentially have huge impacts on society at large. As members of society, you will be faced with those impacts and with decisions about them regardless of your choice of career.
I have designed Biology 311 to integrate these three aspects of molecular biology. We will spend a lot of our time on content&emdash;building a basic understanding of the state of this field as it is today. This will serve as your foundation. Whenever possible, this content will be provided in its experimental context, to give you an idea of the process that built it. In other words, we'll discuss not only what we know, but how we know it. In each of the four final units in the course, we will also read and discuss an article from the primary research literature in molecular biology. We'll pick these papers apart to determine what the underlying questions were, how these questions were addressed, what the data showed, and whether the conclusions are supported. These papers and discussions will give you a chance to develop and refine your science "process" skills. Finally, we'll step back now and then to discuss social context&emdash;the interplay between the field of molecular biology and society as a whole, and the impact each has on the other. My overall goals for you are as follows:
1. To gain a solid understanding of existing concepts in molecular biology, including an idea of how these concepts were developed by scientists over time.
2. To gain proficiency, confidence, and experience in reading and analyzing primary research literature in molecular biology.
3. To increase your sophistication on issues of societal importance which involve molecular biology and related technologies, as well as your confidence and experience in thinking and talking about these issues.
Your responsibilities (as I see them):
I cannot emphasize this last point enough! Please, you must not be shy. I expect you to make clear to me when you do not understand something, preferably by asking questions in class where others may benefit. Alternatively, come see me in my office or send me a note by e-mail. You should never feel a question is too trivial to ask. Most likely, I have explained it in a way that leaves out just one crucial link for you, and it can often be something missing for others as well. Asking questions not only helps you learn, it also helps me teach.
Research has shown that one of the least effective ways to further understanding is to sit passively and listen to a lecture, no matter how well-organized and clear the lecture may be. Your own experience may bear this out. If you wanted to learn to make quiche, for example, which do you think would be more effective&emdash;watching a beautifully presented program on public television or going into the kitchen and attempting to follow a quiche recipe?
Its not that you wouldnt be interested in the TV program, or motivated to learn from it. Rather, it is simply that the more different ways you can engage your brain in processing a concept the more effectively you learn. Doing something is more effective than reading about it, and explaining something is more effective yet.
If you are to gain an understanding of molecular biology, you must actively engage the material. What does this mean?
Starting class at 8am. Class starts at 8 am. This may not be your favorite time of day&emdash;it's not mine. This is the time that we have together, though, and we need to make the most of it. So do what you need to do to get yourself in the classroom, notebook open, brain engaged, ready to go at 8 sharp. The extra effort will be worth your while.
Evening exams. In order for me to be able to assess whether you have been able not only to memorize, but also to synthesize and make use of new information, I need to be able to ask complex questions on our exams. Feedback that I have received from students in the past has been that it can be difficult to complete such an exam within a one-hour time frame, that it is challenging to process complex tasks at 8 am, and that more questions with fewer points attached to each would be appreciated. To accommodate this, I have scheduled our midterms as two-hour evening exams, from 7 &endash; 9 pm. Please check your schedules now to ensure that you will be able to attend these exams. If these times pose a problem for you, simply contact me to make other arrangements. For you to receive credit for the exam, we must have agreed upon an alternate arrangement by 5 pm on the Friday preceding the exam. Except in cases of medical emergency or death in your immediate family, failure to make advance arrangments with me will result in a grade of zero for any exam missed. The final exam cannot be rescheduled or taken at an alternate time. Please take this into account when making your end-of-semester travel arrangements. (And please note that Bio312 will have a separate final exam.)
At this point, take a break from reading the syllabus and send me an e-mail telling me whether the Monday evening exams are going to work for you. If I receive your e-mail by 5 pm on Monday, Sept 11th, you will receive 5 pts extra credit. It's my way of saying thank you for your diligence in attending to these matters.
Late assignments. Assignments are due at the beginning of class on the day stated on the assignment. They will not be accepted late. To accomodate the fact that emergencies will arise, I will drop your lowest score on each set of assignments before calculating your final grade.
Student evaluation
Midterm I (Thurs, Oct 5)
100 Pts
Midterm II (Mon, Nov 13)
100 Pts
Final Exam
180 Pts
Question sets on outside readings (6 @ 10 pts, lowest dropped)
50 Pts
Text-based homework assignments (8 @ 10 pts, lowest dropped)
70 Pts
Total:
500 pts
Grading Scale
Exams in this course will not be graded on a curve. You are not in competition with your fellow students, only with the material. The grade cut-offs will be as follows:
450-500pts
A
441-449pts
A-
435-440pts
B+
400-434pts
B
391-399pts
B-
385-390pts
C+
350-384pts
C
333-349pts
C-
250-332pts
D
A problem that be encountered with "non-curved" grades is that the instructor can misjudge and write an exam that is too difficult for most students. To compensate for this problem, if I write an exam on which the mean score is less than 75%, I will adjust the scores for that exam upward so that the mean score is 75%.
revised Friday, October 13th
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Wed, Sept 6 |
Welcome, introductions, expectations |
Review: CH 4 |
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Fri, Sept 8 to Mon, Sept 18 |
Molecular biology techniques |
CH 7 |
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Wed, Sept 20 |
Discussion of outside reading: "The Function of Dogma in Scientific Research" by Thomas Kuhn |
On reserve at Watzek |
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Fri, Sept 22 to Mon, Oct 2 |
Chapter 7 wrap-up (9/22) and Molecular genetics (9/25 - 10/2) |
CH 8 |
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Wed, Oct 4 |
Review for Exam I |
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Thursday, Oct 5, 7 to 9 pm |
EXAM I (BoDine 300) |
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Mon, Oct 9 to Wed Oct 11 |
Gene structure |
CH 9 |
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Mon, Oct 16 |
Gene structure continued (CH 9 wrap-up) |
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Wed, Oct 18 |
Discussion of Outside Reading: "A new S cerevisiae ankyrin repeat-encoding gene" by Lycan et al |
On reserve at Watzek |
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Fri, Oct 20 to Fri, Oct 27 |
Regulation of transcription initiation |
CH 10 |
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Mon, Oct 30 |
Discussion of outside reading: Jacob et al, 1960 |
On reserve at Watzek |
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Wed, Nov 1 to Wed, Nov 8 |
Post-transcriptional regulation |
CH 11 |
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Fri, Nov 10 |
Discussion of outside reading: post-transcriptional control |
To be assigned |
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Mon, Nov 13 |
Review for Exam II |
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Monday, Nov 13, 7 to 9 pm |
EXAM II (BoDine 300) |
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Wed, Nov 15 to Wed, Nov 22 |
DNA replication, repair, and recombination (guest lecturer: Dr. Suzanne Deschenes) |
CH 12 |
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Fri, Nov 24 |
THANKSGIVING BREAK |
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Mon, Nov 27 |
Discussion of outside reading: DNA repair research |
To be assigned |
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Wed, Nov 29 to Fri, Dec 8 |
Regulation of development |
CH 14 |
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Mon, Dec 11 |
Discussion of outside reading: research in developmental biology |
To be assigned |
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Wed, Dec 13 |
Review for final exam |
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SAT, Dec 16, 6 to 8 pm |
FINAL EXAM |
Except for exam dates, schedule is subject to adjustment and revision to suit the needs of the class
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Created by:
bkbaxter@lclark.edu
Updated: 19 Oct 00