1 / 25

Eukaryotic Gene Regulation

Eukaryotic Gene Regulation. Chapter 18. Overview. Eukaryotes can regulate gene expression at multiple stages from gene to functional protein Regulation of chromatin structure DNA methylation Transcription initiation factors Alternative RNA processing Protein degradation. -- blue = DNA

perry-avery
Télécharger la présentation

Eukaryotic Gene Regulation

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. Eukaryotic Gene Regulation Chapter 18

  2. Overview • Eukaryotes can regulate gene expression at multiple stages from gene to functional protein • Regulation of chromatin structure • DNA methylation • Transcription initiation factors • Alternative RNA processing • Protein degradation

  3. -- blue = DNA -- orange = RNA -- purple = protein --Each of these is a possible site for regulation, but not all are used in any instance or cell

  4. How do we get different cell types? • Red blood cells, muscle cells, neurons… • Every cell has the same genes • Different cells express only a fraction of their genes • 20% of cell’s genes are expressed

  5. Histone Acetylation -- DNA level of regulation -- Histone proteins have protruding “tails” -- Acetyl groups can be added to these tails -- Acetylated histones lose their + charge, and are unable to bind to other nucleosomes -- Acetylated histones = transcription more likely

  6. Histone Code Hypothesis • Histone tails can be • Acetylated, methylated, or phosphorylated • Methylation = condensation of chromatin • Phosphorylation = separation of histones • So which determines the proteins produced: acetylation or the specific combination of these modifications?

  7. DNA Methylation • DNA itself can be methylated as well • Actually methyl groups are attached to the nitrogenous bases of nucleotides • Specifically cytosine • Methylated bases are not able to be expressed • Remember methylation from Inactivated X chromosomes? • Interfere with normal methylation = weird results

  8. Important Difference… • Histone acetylation = INCREASED transcription • DNA methylation = DECREASED transcription

  9. Why are identical twins different? • They have the same genome, so WTF? • Base-pair mutations are one way to get genetic diversity • Different DNA sequences may be methylated, this results in certain sequences being turned off • So same DNA but phenotypic variation • Identical twins, but one has schizophrenia while the other does not • Called epigenetic inheritance (traits that are NOT contained on nucleotide sequences)

  10. Transcriptional Modification • Most important area of regulation or control of gene expression • Was this true in prokaryotes? • Involves Enhancer regions on the DNA • Activator proteins bind to mediator proteins • The complex is called transcription initiation complex • Transcription of the downstream regions is enhanced

  11. -- Activator proteins bind to the enhancer region of DNA -- Activator proteins also bind to Mediator proteins + Transcription factors -- Forms transcription initiation complex -- Almost guarantees that the gene will be expressed

  12. -- Activator proteins bind to enhancer DNA region -- Different activator proteins = different gene transcribed & expressed -- Activator proteins = directors of transcription in eukaryotes

  13. Alternative RNA Splicing -- Spliceosomes can splice the primary RNA transcript differently -- Creates different proteins -- Fruit fly gene = 38,000 different combinations of proteins -- Yet again, is phenotypic variation due to genetic sequences?

  14. siRNA Cure for Ebola? • 1.5% of genome codes for proteins • Even smaller amount codes for RNAs (tRNA, mRNA, rRNA) • So is any part of the 98% ever transcribed?

  15. miRNA • microRNAs are capable of binding complementary sequences in mRNA molecules • Usually degrades the mRNA it binds OR blocks translation of the mRNA • 1/3 of all genes regulated via miRNAs

  16. RNA Interference (RNAi) • Inject dsRNA molecules into a cell • This turns off gene expression of those genes with same sequence as the dsRNA • Small Interfering RNA (siRNA) were the dsRNA responsible for the interference • How did this lead to a treatment for Ebola? • Ebola is an RNA based virus • What about HIV? Hepatitis A or C? common cold? • Dengue fever? influenza? H1N1, H5N1?

  17. Skip 18.4

  18. Cancer Genes • Oncogenes = cancer-causing genes • Proto-oncogenes = genes that codes for proteins that promote normal cell growth • Proto-oncogenes can become oncogenes • Leads to an increase in protein production • OR an increase in the activity of normal protein production • Either leads to TOO MUCH mitosis

  19. Tumor-Suppressor Genes • The produced proteins inhibit cell division • If a mutation decreases production of these products, cell division will accelerate • 2 ways to get neoplastic growths (cancer): • Mutation which alters proto-oncogenes into oncogenes • Over-produces protein OR hyperactive protein production • This interferes with usual mechanism of cell cycle regulation • Mutation interferes with tumor-suppressor genes • Insufficient production leads to mitotic hyperactivity

  20. Again…

  21. Cell Cycle Stimulator Pathway Mutation in ras? -- Activity even though no growth factor has been received by the RTK -- Outcome = Excessive Mitosis

  22. p53 gene -- Commonly called the “guardian angel of the genome” -- Halts cell cycle by binding CdK proteins -- Allows time for DNA repair --p53 is also directly involved in DNA repair --p53 initiates apoptosis if DNA damage is beyond repair

  23. MultiStep Model of the Development of Colorectal Cancer

More Related