Friday, December 10, 2010

Lecture, chapter 4 - Genes, genomes, and DNA



Organization of the human genome
from Allison, L. 2007. Fundamental Molecular Biology. Blackwell Publishing.
(click on pic for a full size image)
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Today we followed our discussion on how DNA is organized in genomes (second stop in our roadmap), including a discussion on satellite DNA (satellites, minisatellites, and microsatellites), palindromic DNA (mirror-like palindromes, inverted repeats, hairpins, stem-and-loops), junk and selfish DNA, and supercoiling.

On Monday we'll discuss how eukaryotic DNA is compacted enough to fit the nucleus of a cell

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Module 1 (section 1)
Lab 3 - PCI DNA extraction from human blood
Lab 4 - PCR of the PV92 Alu insertion locus

Lab 3 - PCI DNA extraction from human blood

Yesterday students finished the PCI DNA extraction from their own blood. The steps that were left included adding the PCI, doing some pellet washes with cold ethanol and eluting the DNA in TE buffer. Samples were incubated overnight at 55ºC.

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Lab 4 - PCR of the PV92 Alu insertion locus

The goal of this lab was to introduce students to the Polymerase Chain Reaction (PCR), the most popular in vitro technique to make copies of (amplify) target DNA fragments. We extracted DNA from our cheek cells and used it to set up PCRs.

Our target is the PV92 Alu insertion locus, located on chromosome 16.
Alu elements are a family of short interspersed repetitive elements (SINEs) that have mobilized throughout primate genomes for the last 65 My, by retrotransposition.

There are more than 500,000 Alu elements per haploid genome in humans (about 5% of our genome). Depending on the insertion point they may be associated with some genetic diseases (e.g. some cases of hemophilia, familial hypercholesterolemia, severe combined immune deficiency, or neurofibromatosis type 1). But in most cases it has no effect on the individual's health.

Some Alu insertions are very recent and polymorphic. The most recent are human specific (HS) and such is the case of PV92. Because the PV92 insertion locus is HS, polymorphic, neutral (invisible for natural selection), and easy to detect, it has been widely used in human genetic population studies, and it has been one of the markers used to support the out-of-Africa hypothesis.

In this lab we will test the presence of 0, 1, or 2 PV92 Alu insertions in our genomes.

The following picture illustrates the possible outcomes of our PCRs:


The sample on lane 1 belongs to an individual with no PV92 Alu insertions, lane 2 to an individual with insertions in both chromosomes, and lane 3 to an individual with an insertion in one chromosome.

What is your genotype like?

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Wednesday, December 8, 2010

Module 1, lab 3 (section 1) - PCI DNA extraction from human blood

Today we started the phenol-chloroform isoamyl alcohol (PCI) DNA extraction from most students' blood. Blood samples were obtained throughout Monday and Tuesday.

Students added SSC buffer (pH stabilization), SDS (cell lysis), sodium acetate (NaOAc; protein precipitation), proteinase K (inactivation of endonucleases), PCI (separation of proteins and nucleic acids), and 100% ethanol (DNA precipitation). Samples were frozen to continue the process tomorrow.

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Tuesday, December 7, 2010

Lecture
Chapter 3 - DNA, RNA, and Proteins
Chapter 4 - Genes, genomes, and DNA

Today we finished chapter 3, mentioning the basics of the different functions of RNA and protein structure.

We then started chapter 4, on genes, genomes and DNA, which is our second strop in the class roadmap: How DNA is organized in organisms and how such organization affects its function.

We discussed how little genetic information is necessary for independent life and the importance of non-coding DNA in eukaryotes. We talked about pseudogenes, introns, and repeated sequences (tandem repeats and intersperse elements).

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Module 1, lab 3 (section 2) - PCI DNA extraction from human blood

Students extracted DNA from their own blood. The entire protocol was completed and samples of DNA eluted in TE buffer were frozen at -20ºC.

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Module 1, lab 2 (section 2) - Size exclusion chromatography

Students did a size exclusion chromatography of a protein sample containing hemoglobin and vitamin B12. For more a more detailed blog entry click here.

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Module 1, lab 1 (section 2) - RED of lambda DNA
Gel electrophoresis

Students completed ran an agarose gel electrophoresis of the restriction enzyme digestion performed last week. For more details check this previous blog entry.

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