Thursday, July 23, 2009

DEVELOPMENTAL GENETICS AND ENHANCER TRAPS

What do you need to remember about developmental genetics?
1) Different cells, and cells in different positions, are different because they express different combinations of genes.

2) How do cells end up expressing different combinations of genes? There are 2 main reasons: 
a) they inherit different cytoplasmic determinants (for example, if in a cell a particular protein is not evenly distributed throughout the cytoplasm, the 2 daughter cells will inherit different concentrations of this protein). In the special cases of embryos that at some point are like the Drosophila one, with many nuclei in a big communal cytoplasm, if a morphogen is distributed unevenly  in the communal cytoplasm, then nuclei in different regions will be exposed to different concentrations of the morphogen. The net result of inheriting, or being exposed to, different concentrations of morphogens is that different genes will be expressed at different levels;
b) cells communicate with each other and with their environment; cell-to-cell communication, and cell-to-environment communication is transduced into signalling cascades, resulting in expression of particular subsets of genes.

3) How can we have uneven distribution of an RNA or of a protein in the cytoplasm? Again, there are a number of ways. We can anchor the RNA to a particular spot, so that when it is translated, the protein product will diffuse from this source and thus form a concentration gradient. We can also constantly, actively transport the RNA or the protein product to one region of the cytoplasm. We can let the RNA get evenly distributed, but have a protein, localized in one specific region and forming a bit of a concentration gradient, that prevents its translation. This will create a 'sink' and therefore a concentration gradient of the protein product of our RNA.

4) Remember maternal effect genes! Remember that at the earliest stages, a zygote does not transcribe/translate its own genes. It 'lives off' the products that the mother dumped in the egg's cytoplasm. 


FOR ENHANCER TRAPS
Here are a few links that, are better than any explanations I gould give, and also give lots of example of how people use these great tools:


Example of uses (just read the abstracts to get an idea!):








7 comments:

  1. Thanks Pam for all your help in both 335 and 334! I really appreciate it!

    Jasmine

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  2. Thanks for answering all our (sometimes annoying and repetitive) questions with patience :)

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  3. Hello Everyone!

    I have a question about cloning. How do we get overlapping region of chromosome? Lets say we isolated DNA to find our gene of interest. Do we isolate lots of DNA(from 4 or 5 chicken) and then we do partial digestion with different enzymes? Or do we have only one DNAfrom only one chicken?

    If we have only one DNA then how do we get overlapping regions?

    Thanks

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  4. Hi PAM!

    Thanks for the awesome two terms! I really enjoyed genetics, didn't before - but I think I do now! Thanks for spending those extra hours after tutorial trying to explain to Tina, Mary, Giny, Angel, and me about the many concepts of 334/335. Hope you enjoy the cookies! Hope to see you again very soon! Enjoy the rest of your summer o! The trip to LSI was an awesome one, thanks!

    Cheers,

    Sam (Peter Parker)

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  5. Hey 335 survivors!

    I had a great time working with you. You were such an enthusiastic (and a little crazy) bunch!
    I am not really allowed to discuss answers until the grades are in, but if you can rephrase your question... (also, you'll have to refresh my memory because I don't remember the order of the questions).

    Cheers

    Pam

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  6. pam i hope your summer is going well! i was hoping you could tell us when our grades will be up! thanks again for all your help.

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  7. Thy should be up sometime this week. The exams are marked, but Craig has got himself injured over the long weekend and could not make it in today to post the grades.

    Cheers

    Pam

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