Friday, February 29, 2008

Sequencing of an entire genome


6 comments:

Anonymous said...

Hi Pam!

I just wanted to say that I felt that Monday's tutorial (March 3) was very useful and helpful doing the extra problems in class together. In my opinion, it was more helpful than the structure of the tutorial the week before or the week that we drew the posters. Thanks!

Anonymous said...

I do also agree with the above comment. in general I fill that tutorials are not helping me to prepare for exam. thanks!

Anonymous said...

Hi Pam,

I was reading about yeast 2 hybrid system...and it states that sometimes yeast 2 hybrids has lots of false positive and false negatives results due to overexpression?, and problems fusion with AD and BD?
What would overexpression mean and problems with yeast 2 hybrids mean?

Anonymous said...

True, the yest 2hyb often gives "falses". If you overexpress a protein, the "surplus" may go bind to DNA sequences or (like in this case) proteins that it does not usually interacts with. So, you would "see" an interaction in the 2 hybrid system, but it would be an artifact of the experimental system, and those two proteins do not actually inetract in "real life".

You may also get "false negatives". Foe example, some proteins cannot bind a protein of interest in the absence of "auxiliary factors" (other proteins), and since these auxiliary factors may not be present in the yeast, they won't produce an interaction in the 2 hyb system, but they may well interact in "real life".

Does this help?

Cheers

Pam

Anonymous said...

hi pam,

how come this blog is not updated anymore since february?

thanks

Anonymous said...

That's a good question.
What would you like to find here? Let me know and I'll make sure it's up.

In the meantime, some Q&A from previous terms are coming...

Thanks for you comment.

Pam