1 / 7

What makes us unique.

There are variations in genes that make us unique. Inversion. Insertion. Deletion. Copy number variation. What makes us unique. Changes in the number and order of genes (A–D) add variety to the human genome. Reference. http://www.sciencemag.org/cgi/reprint/318/5858/1842.pdf.

milica
Download Presentation

What makes us unique.

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. There are variations in genes that make us unique Inversion Insertion Deletion Copy number variation What makes us unique. Changes in the number and order of genes (A–D) add variety to the human genome Reference http://www.sciencemag.org/cgi/reprint/318/5858/1842.pdf

  2. NOW WE UNDERSTAND THE ROLE OF CFTR… WHAT ABOUT GENES THAT MODIFY CF? Genes can have variation that does not necessarily cause disease. These variations may have an effect on how much protein it produced or how well that protein works. In an otherwise healthy person, this variation may have little or no effect. In a person with a disease like CF, this variation may modify the severity of the CF symptoms. Genes that modify CF symptoms are called modifier genes.

  3. Modifier Genes in CF The CF Twin and Sibling Study is looking for genetic variation that is linked with CF. It is important that we study families, not just individuals diagnosed with CF. If we know the parent’s genetic variation, we can then study what combinations of genetic variation they give to their children.

  4. Modifier Genes in CF We also examine what genetic variation siblings do and do not share. We then compare the genetic variation with symptoms. Where these pieces of information line up in the family (shared variations and shared symptoms) give clues for genes that may affect CF disease.

  5. www.sph.umich.edu/.../fall07/inFOCUS/four.htm www.sph.umich.edu/.../fall07/inFOCUS/four.htm www.sph.umich.edu/.../fall07/inFOCUS/four.htm Modifier Genes in CF CF patients live in their own unique environments (smoking, diet, and exposure to pollutants). Using families also helps us sort out which CF symptom differences are caused by genetic factors, caused by environmental factors, or caused by a combination of genes and environment. www.sph.umich.edu/.../fall07/inFOCUS/four.htm

  6. SO? Finding other genes (like the ones that effect Diabetes, BMI, Lung Disease) will help us to understand why symptoms happen and help us to predict those symptoms. We can then design treatments or medicines based on personal risks.

  7. The Future Individuals respond differently to drugs and sometimes the effects are unpredictable. Differences in DNA…targeted by drugs can contribute significantly to variation in the responses of individuals… This intersection of genomics and medicine has the potential to yield a new set of molecular diagnostic tools that can be used to individualize and optimize drug therapy. William E. Evans and Mary V. Relling. Moving towards individualized medicine with pharmacogenomics. Nature429, 464-468 (27 May 2004)

More Related