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Campbell 7th Edition - Chapter 19 Eukaryotic Genomes: Organization, Regulation, and Evolution Flashcards

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1242824964What is the order of packaging of DNA from first to last?Histones to Nucelosomes to 30 nanometer chromatin to loops to chromosome.0
1242824966The following are characteristics of histones.1. Are responsible for the first level of DNA packing in chromatin. 2. Are in groups of 8 histones per nucleosome. 3. Have protein unit H 1 linker protein.1
1242824968Levels of regulation of gene expression are:1. Chromatin Structure 2. Transcription Initiation 3. Post-transcription2
1242824970Histone modificationChemical modification of histone tails can affect the configuration of chromatin by exposing DNA and thus allowing gene expression.3
1242824972What is histone acetylation?Acetylation of histone tails promotes loosening chromatin structure that permits transcription, by removing the positive charge of the histone, decreasing the interaction with the negative charges of the DNA phosphate backbone.4
1242824974What is histone methylation?Histone methylation is in general associated with transcription repression, such as methylation of cytosine.5
1242824976Epigenetic inheritanceInheritance that is Non-mendelian, non-mutational, not based on DNA sequence.6
1242824978Transcription factorsproteins that Assist DNA polymerase in transcription.7
1242824980ActivatorsProtein that binds to enhancer regions also called distal control elements and speed up the rate of transcription.8
1242824982RepressorsProtein that binds to silencer regions and slow down the rate of transcription.9
1242824984Basal transcription factors.Position RNA polymerase at the start position for to initiate transcription.10
1242824986CoactivatorsAssist in signal transmission of activators or repressors.11
1242824988Post-Transcriptional Regulations include:1. RNA processing 2. mRNA degradation (miRNAs) 3. Initiation of translation 4. Protein processing and degradation12
1242824990alternative RNA splicingDescribes when different mRNA molecules are produced from the same primary transcript, depending on which RNA segments are treated as exons and which as introns.13
1242824993microRNAs (miRNAs)single stranded, small segments of RNA that attach to mRNA to disable transcription or degrade the mRNA14
1242824995Proteasomesgiant protein complexes that bind protein molecules and degrade them, example Ubiquitin.15
1242824997Cancer-causing genesOncogenes16
1242824999Proto-oncogenesNormal cellular genes that code for proteins for normal cell growth and division but if mutated becomes oncogene.17
1242825001Four ways to convert a proto-oncogene to an onco gene:1. translocation of gene to new locus. 2.excessive gene amplification. 3. point mutation within a controlling element. 4. point mutation within the gene.18
1242825003Tumor-suppressor genesEncode proteins that inhibit abnormal cell division, example is p53 gene.19
1242825005Ras gene Ras pathwayA cell stimulating pathway that when mutated can cause uncontrolled stimulation of cells.20
1242825007p53 geneA tumor suppressor. A cell inhibiting pathway that blocks DNA replication of damaged DNA, when mutated is unable to block DNA replication of damaged DNA, leading to excessive growth and cancer.21
1242825009Transposable ElementsAlso known as transposons, jumping genes, are DNA segments that can change its position within a genome.22
1242825011RetrotransposonsJumping genes which move within a genome by means of an RNA intermediate.23
1242825013The classic examples of multigene families of nonidentical genes.Alpha and Beta Hemoglobins, each from a different gene family, from chromosome 16 and 11..24
1242825016DNA mutationsUnderlies much of genome evolution25
1242825018Transposable elementsMay be involved in genome evolution; they constitute two-thirds of the human genome.26
1245521626Fetal programmingFetus is exposed to prenatal environment that modifies gene expression.27

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