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i. Transcription and its Regulation
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triple-november-equal-high-emma-monkey
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07/28/2024
The {{c1::HOX}} gene is a series of genes that when expressed define developmental patterns along the anteroposterior axis. The encoded {{c2…
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The {{c1::Sonic hedgehog Shh}} is a secreted protein molecule that diffuses to form a concentration gradient starting at the {{c2::zone of p…
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Synpolydactyly (SPD) is a disorder with an {{c1::autosomal dominant}} inheritance pattern.
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Explain the cause of synpolydactyly
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PIC stands for {{c1::Pre-Initiation Complex}}
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An activator protein has 2 domains:
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What is Chromatin Immunoprecipitation (ChIP) used for?
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CRE stands for the {{c1::Cyclic-AMP Response Element}}
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The {{c1::CRE}} is a cis-element, (a DNA sequence that regulates the transcription of a neighboring gene) that is located near many promoters for…
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CREB stands for {{c1::Cyclic AMP Response Element-Binding protein}}
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{{c1::CREB}} is a transcription factor that binds to the CRE cis element
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CBP stands for {{c1::CREB bind protein}}
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{{c1::CBP}} is a co-activator and histone acetylation writer that does not bind DNA but binds CREB when CREB is phosphorylated and increases transcrip…
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A {{c1::mediator}} is a key protein connectivity complex that allows for many different transcription factors to communicate with the polymerase
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By what 3 mechanisms can a repressor work?
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{{c1::Co-activators/repressors}} do not themselves bind directly to DNA, but function to regulate transcription of genes via binding to the general tr…
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For CBP to bind CREB, CREB must first be {{c1::phosphorylated}}
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{{c1::Focused}} transcription initiation typically is regulated by a {{c2::TATA box}} in the promoter region
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{{c1::Dispersed}} transcription initiation typically is regulated by {{c2::CpG islands}} in the promoter regions
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Focused transcription is more commonly used for?
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Dispersed transcription initiation is typically used for?
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The histone octamer is typically composed of pairs of the following 4 subunits:
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The acetylation of histone tails is associated with {{c1::active}} genes
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HATs stands for {{c1::Histone aceyltransferases}}
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HDACs stands for {{c1::Histone deacetylases}}
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{{c1::Histone Acetyl Transferases}} acetylate histone tails
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{{c1::HDACs}} de-acetylate histone tails
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2 examples of HATs are:
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Histone acetylation occurs at the {{c1::lysine}} residues of the histone tail thereby removing the positive charge of {{c1::lysine}} which reduce…
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{{c1::CBP}} is an example of a histone acetylation {{c2::writer because it also has histone acylation activity along with the activity to bind to…
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{{c1::HDACs}} are an example of histone acetylation {{c2::eraser}}
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{{c1::bromo domain proteins}} are an example of a histone acetylation {{c2::reader}}
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{{c1::bromodomains}} with reader complexes bind to specific acetylated lysine residues in specific histone sequences to recruit other associated chrom…
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A {{c1::chromatin remodeler}} is an enzyme that is stimulated by the presence of DNA to hydrolyze ATP, which can then be used as energy source to…
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A {{c1::histone chaperone}} is a family of proteins that binds to either a H2A-H2B dimer or to a H3-H4 tetramer to prevent inappropriate aggregat…
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A {{c1::histone variant}} is a protein that is almost identical to one of the four core canonical histone genes with specific amino acid changes …
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What is the function of the SWI/SNF chromatin remodeling complex?
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{{c1::ATRX}} is a histone methylation reader at H3K9me3 and H3K4me0 that recruits the {{c2::DAXX}} histone chaperone to insert the variant histon…
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The histone {{c1::H2A.Z}} facilitates TBP binding (TFIID subunit) and increases gene expression
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The histone {{c1::H3.3}} is enriched near the promoter of some actively transcribing genes and represents the majority of H3K4me modified subunit…
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The {{c1::SWR-C}} complex exchanges the variant histone {{c2::H2A.z for H2A}} at the promoter region
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The {{c1::HIRA}} complex facilitates {{c2::H3.3}} deposition at both promoters and downstream particularly during muscle development (same a…
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{{c1::lysine and arginine}} residues may be methylated during histone methylatation
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{{c1::SUV39H1}} is a histone methylation (H3K9) writer and mutated in cases of {{c2::retinoblastoma}}
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{{c1::JHDM}} is a demethylase (H3K9) (Histone methylation eraser); mutations of which are responsible for {{c2::male infertility}} and {{c3:…
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DNA methylation occurs at the {{c1::C5}} position of {{c2::cytosine}} found in {{c3::CpG islands}}
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5meC can spontaneously deaminate to form {{c1::thymine}}; hence CpGs are {{c2::under}}-represented compared to their expected frequency
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Non-methylated CpGs typically overlap with {{c1::promoter regions}}
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5meC's recruit {{c1::methyl binding domain proteins (MBDs)}} and other potential transcription inhibitory proteins to turn off the gene. The inhi…
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{{c1::Rett syndrome}} is an x-linked neurodevelopmental syndrome due to mutations in the gene for {{c2::MeCP2 (Methyl-CpG-Binding Protein 2)}}
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MeCP2 (a methyl binding domain protein) binds to {{c1::5meCs}} in selected CGIs and recruits transcription repression factors such as {{c2::…
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{{c1::phosphorylation}} can cause MeCP2 dissociation and gene activation
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Histone methylation on lysine {{c1::H3K4}} always activates the gene
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Mono methylation on the histone lysine {{c1::H3K27}} will promote activation of the gene
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How does DNA methylation play a role in genomic imprinting?
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Rubinstein Tabi Syndrome is caused by a spontaneous deletion in the {{c1::CBP gene}}
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