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BEGR 424 Molecular Biology William Terzaghi Spring, 2016. BEGR424- Resource and Policy Information Instructor: Dr. William Terzaghi Office: SLC 363 / CSC228 Office hours: MWF 12:00-1:00, TR 1-2 or by appointment Phone: (570) 408-4762 Email: terzaghi@wilkes.edu.
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BEGR 424 Molecular Biology William Terzaghi Spring, 2016
BEGR424- Resource and Policy Information Instructor: Dr. William Terzaghi Office: SLC 363/CSC228 Office hours: MWF 12:00-1:00, TR 1-2 or by appointment Phone: (570) 408-4762 Email: terzaghi@wilkes.edu
BEGR424- Resource and Policy Information Instructor: Dr. William Terzaghi Office: SLC 363/CSC228 Office hours: MWF 12:00-1:00, TR 1-2 or by appointment Phone: (570) 408-4762 Email: terzaghi@wilkes.edu Course webpage: http://staffweb.wilkes.edu/william.terzaghi/BEGR424.html
General considerations What do you hope to learn?
General considerations • What do you hope to learn? • Graduate courses • learning about current literature
General considerations • What do you hope to learn? • Graduate courses • learning about current literature • Learning how to give presentations
General considerations • What do you hope to learn? • Graduate courses • learning about current literature • Learning current techniques
General considerations • What do you hope to learn? • Graduate courses • learning about current literature • Learning current techniques • Using them!
Provide a genuine experience in using cell and molecular biology to learn about a fundamental problem in biology.
Provide a genuine experience in using cell and molecular biology to learn about a fundamental problem in biology. • Rather than following a set series of lectures, study a problem and see where it leads us.
Provide a genuine experience in using cell and molecular biology to learn about a fundamental problem in biology. • Rather than following a set series of lectures, study a problem and see where it leads us. • Lectures & presentations will relate to current status
Provide a genuine experience in using cell and molecular biology to learn about a fundamental problem in biology. • Rather than following a set series of lectures, study a problem and see where it leads us. • Lectures & presentations will relate to current status • Some class time will be spent in lab & vice-versa • we may need to come in at other times as well
Pick a problem Design some experiments
Pick a problem Design some experiments See where they lead us
Pick a problem Design some experiments See where they lead us Grading? Combination of papers and presentations
GRADING? • Combination of papers and presentations • First presentation: 5 points • Research presentation: 10 points • Final presentation: 15 points • Assignments: 5 points each • Poster: 10 points • Intermediate report 10 points • Final report: 30 points • Alternatives • Paper(s) instead of 1 or two presentations • Research proposal instead of a presentation • One or two exams?
Topics? • Trying to find another way to remove oxalate • Making a probiotic bacterium that removes oxalate • Identifying best candidates • Figuring out how to engineer them • Add oxalate transporter? • Add more/different oxalate altering enzymes? • Target them to different locations?
Topics? • Trying to find another way to remove oxalate • Making a probiotic bacterium that removes oxalate • Engineering magnetosomes to express novel proteins • Membrane-bound single-domain iron-oxide crystals made by magnetotic bacteria to help find correct pO2
Topics? • Trying to find another way to remove oxalate • Making a probiotic bacterium that removes oxalate • Engineering magnetosomes to express novel proteins • Membrane-bound single-domain iron-oxide crystals made by magnetotic bacteria to help find correct pO2 • Can engineer Mms13-fusion proteins
Topics? • Trying to find another way to remove oxalate • Making a probiotic bacterium that removes oxalate • Engineering magnetosomes to express novel proteins • Studying ncRNA • Making Crispr/CAS9 proteins • Mutate/replace specific genes • Bind specific DNA sequences • Color code with fluorescent proteins • Repress expression • Make transcriptional activators by fusing with activation domains
Topics? • Trying to find another way to remove oxalate • Making a probiotic bacterium that removes oxalate • Engineering magnetosomes to express novel proteins • Studying ncRNA • Studying sugar signaling
Topics? • Trying to find another way to remove oxalate • Making a probiotic bacterium that removes oxalate • Engineering magnetosomes to express novel proteins • Studying ncRNA • Studying sugar signaling • Bioremediation • Atrazine • Neonicotinoid pesticides • Something else??
Topics? Trying to find another way to remove oxalate Making a probiotic bacterium that removes oxalate Engineering magnetosomes to express novel proteins Studying ncRNA Studying sugar signaling Bioremediation Making plants/algae that bypass Rubisco to fix CO2
Topics? • Trying to find another way to remove oxalate • Making a probiotic bacterium that removes oxalate • Engineering magnetosomes to express novel proteins • Studying ncRNA • Studying sugar signaling • Bioremediation • Making plants/algae that bypass Rubisco to fix CO2 • Making novel biofuels • blue-green algae that generate electricity • Plants/algae that make methane or hydrogen • Biodiesel • Other ideas???
Topics? Trying to find another way to remove oxalate Making a probiotic bacterium that removes oxalate Engineering magnetosomes to express novel proteins Studying ncRNA Studying sugar signaling Bioremediation Making plants/algae that bypass Rubisco to fix CO2 Making novel biofuels Making vectors for Dr. Harms Something else?
Assignments? identify a gene and design primers presentation on new sequencing tech designing a protocol to verify your clone presentations on gene regulation presentation on applying mol bio Other work draft of report on cloning & sequencing poster for symposium final gene report draft of formal report formal report
Genome Projects Studying structure & function of genomes
Genome Projects • Studying structure & function of genomes • Sequence first
Genome Projects • Studying structure & function of genomes • Sequence first • Then location and function of every part
Genome Projects • How much DNA is there? • SV40 has 5000 base pairs • E. coli has 5 x 106 • Yeast has 2 x 107 • Arabidopsishas 108 • Ricehas 5 x 108 • Humans have 3 x 109 • Soybeans have 3 x 109 • Toads have 3 x 109 • Salamanders have 8 x 1010 • Lilies have 1011
Genome Projects • C-value paradox: DNA content/haploid genome varies widely
Genome Projects • C-value paradox: DNA content/haploid genome varies widely • Some phyla show little variation: • birds all have ~109bp
Genome Projects • C-value paradox: DNA content/haploid genome varies widely • Some phyla show little variation: • birds all have ~109bp • mammals all have ~ 3 x 109 bp
Genome Projects • C-value paradox: DNA content/haploid genome varies widely • Some phyla show little variation: • birds all have ~109bp • mammals all have ~ 3 x 109 bp • Other phyla are all over: • insects and amphibians vary 100 x
Genome Projects • C-value paradox: DNA content/haploid genome varies widely • Some phyla show little variation: • birds all have ~109bp • mammals all have ~ 3 x 109 bp • Other phyla are all over: • insects and amphibians vary 100 x • flowering plants vary 1000x
C-value paradox • One cause = variations in chromosome numbers and ploidy • 2C chromosome numbers vary widely • Haplopappus has 2
C-value paradox • One cause = variations in chromosome numbers and ploidy • 2C chromosome numbers vary widely • Haplopappus has 2 • Arabidopsis has 10
C-value paradox • One cause = variations in chromosome numbers and ploidy • 2C chromosome numbers vary widely • Haplopappus has 2 • Arabidopsis has 10 • Rice has 24 • Humans have 46 • Tobacco (hexaploid) has 72 • Kiwifruit (octaploid) have 196
C-value paradox Chromosome numbers vary So does chromosome size!
C-value paradox Chromosome numbers vary So does chromosome size! Reason = variation in amounts of repetitive DNA
C-value paradox Chromosome numbers vary So does chromosome size! Reason = variation in amounts of repetitive DNA first demonstrated using Cot curves
Cot curves • denature (melt) DNA by heating
Cot curves • denature (melt) DNA by heating • dissociates into two single strands
Cot curves • denature (melt) DNA by heating • Cool DNA
Cot curves • denature (melt) DNA by heating • Cool DNA:complementary strands find each other &anneal
Cot curves • denature (melt) DNA by heating • Cool DNA:complementary strands find each other &anneal • hybridize
Cot curves • denature (melt) DNA by heating • Cool DNA:complementary strands find each other &anneal • Hybridize: don't have to be the same strands
Cot curves • denature (melt) DNA by heating • Cool DNA:complementary strands find each other &anneal • Hybridize: don't have to be the same strands • Rate depends on [complementary strands]