Gene Expression regulation Flashcards
What are the different eukaryotic DNA control elements?
DNA elements that act locally:
- TATA box,
- promotor proximal elements,
- ehancers
What is the TATA box
a sequence “TATAAA” about 30 bp upstream of start site. This is where TFs bind, it determines txn initiation site and directs RNA pol II binding
What are promoter proximal elements
Generally located within 200 bps upstream of transcription start site and are ~ 20 bps long. Promoter proximal elements help to regulate transcription, and can bound by factors in a cell type specific manner.
What are enhancers?
Contain multiple control elements, each 8-20 bps long. enhancer can be 100-200 bps long. An enhancer can be 200-tens of kilobases upstream or downstream from the promoter or the last exon of the gene, or within an intron. enhancers may help to regulate transcription in a cell type specific manner
Diseases that arise from mutations in DNA control elements
Thalassemias, Hemophelia B. leyden, fragile X syndrome
What are the roles of transcriptional activators and repressors?
Proteins than diffuse and affect transcription of genes, either through activation or repression
What are the two classes of activators and repressors
- sequence specific DNA binding proteins that bind to promoter or enhancer elements usually 6-8 base pairs long. Usually bind DNA by inserting their alpha-helices into the major groove of DNA, making contacts between the amino acid side chains of the protein and the bases in the DNA.
- co factors. Bind to sequence specific DNA binding (not directly to DNA)
What are the 4 basic types of DNA binding domain motifs and what characterizes them?
- Homeodomain (helix-turn-helix): there are 3 helices, two are parallel, the other is perpendicular to those.
- Zinc finger: 3 loops of protein, each of which has one alpha helix associated with it. these loops are held together by four cysteins binding to a zinc ion.
- Basic leucine zipper: dimer of two linearly shaped proteins that “zip” together on either side of the DNA. they have small basic AA tails to recognize and bind DNA
- Helix loop Helix: Similar to Bzip, but it has a out loop in the middle.
Describe the domains of a sequence specific DNA binding protein.
They have a DNA binding domain and protein binding (activation or repression) domain
What are the two classes of Chromatin remodelling factors and how to they work.
- DNA dependent ATP-ase (SWI/SNF): disrupt histone octomers and DNA, reposition nucleosomes on DNA
- Histone modifiers, though acetylation or deacytlation (and methylation)
what is a HAT and how does it work?
Histone acetyl transferase, coactivators- acetylate N-termini of histones. acetylating the N-temini of histones would neutralize the positively charged ends and eliminate electrostatic interactions with DNA phosphates (thus opening up nucleosomal DNA for general transcription factors/Pol II transcriptional apparatus). A currently more favored model is that the acetylation of lysines allows for the binding of specific transcription factors
What is HDAC and how does it work?
Histone deacetylases, corepressors, When HDAC is active, histones retain positive charge at N-terminal ends (HDACS remove acetyl groups from histones), The original thought was that this would maintain the interaction with DNA and prevent access of transcription factors to promoter. A currently more favored model is that the acetylation of lysines allows for the binding of specific transcription factors
What is a disease where histone acetylation is altered?
Rubinstein-Taybi Syndrome, and leukemia
How do activators/repressors modulate transcription via their interaction with general transcriptional machinery vs. with chromatin.
General transcription factors can recruit HATs or HDACs, which then acetylate and alter the structure chromatin/histones to affect gene expression. Some TFs can switch being activators or repressors depending on whether they recruit HAT or HDAC
What is combinatorial control as applies to Transcription factors?
Multiple transcription factors act in different combinations in different cell types, in response to different stimuli, and at different times to provide more fine tuned control of gene expression