Presentation on theme: "Section D - Prokaryotic and Eukaryotic Chromosome Structure."— Presentation transcript:
Section D - Prokaryotic and Eukaryotic Chromosome Structure
D1 Prokaryotic chromosome structure The Escherichia. coli chromosome, DNA domains, Supercoling of the genome, DNA-binding proteinsThe Escherichia. coli chromosomeDNA domainsSupercoling of the genomeDNA-binding proteins D2 Chromatin Structure Chromatin, Histones, Nucleosomes, The role of H1, Linker DNA, The 30 nm fiber, Highter order structureChromatinHistonesNucleosomesThe role of H1Linker DNAThe 30 nm fiberHighter order structure D3 Eukaryotic Chromosomal Structure The mitotic chromosome, The centromere, Telomeres, Interphase chromosome, Heterochromatin, Euchromatin, DNase Ⅰ hypersensitivity, CpG methylation, Histone variants and modificationThe mitotic chromosomeThe centromereTelomeresInterphase chromosomeHeterochromatinEuchromatinDNase Ⅰ hypersensitivityCpG methylationHistone variants and modification D4 Genome complexity Noncoding DNA, Reasociation Kinetics, Unique sequence DNA, Tandem gene clusters, Dispersed repetitive DNA, Satellite DNA, Genetic polymorphismNoncoding DNAReasociation KineticsUnique sequence DNA Tandem gene clustersDispersed repetitive DNASatellite DNA Genetic polymorphism D5 The flow of genetic information The central dogma, Prokaryotic gene expression, Eukaryotic gene expressionThe central dogmaProkaryotic gene expressionEukaryotic gene expressionContents
D1 Prokaryotic chromosome structure — The Escherichia. coli chromosome A single closed-circular DNA, 4.6Mp The DNA packaged into a region known as Nucleoid that contains high concentration of DNA (up to mg/ml) as well as all proteins associated with DNA. Continuous replication (no cell cycle)
D1 Prokaryotic chromosome structure — DNA domains Observed under electron microscopeObserved under electron microscope domains or loops per E. coli chromosome, with kb/loop domains or loops per E. coli chromosome, with kb/loop The ends of loops are constrained by binding to a structure which probably consists of proteins attach to part of the cell membrane.The ends of loops are constrained by binding to a structure which probably consists of proteins attach to part of the cell membrane.
D1 Prokaryotic chromosome structure — Supercoling of the genome E. coli chromosome as a whole is negatively supercoiled.E. coli chromosome as a whole is negatively supercoiled. Individual domains may be supercoiled independently (topological independent).Individual domains may be supercoiled independently (topological independent). Direct biochemical evidence is lacking for different level of supercoiling in different domains.Direct biochemical evidence is lacking for different level of supercoiling in different domains.
D1 Prokaryotic chromosome structure — DNA-binding proteins Histone-like proteins essential for DNA packaging to stabilize and constrain the supercoiling. HU: a small basic dimeric ( 碱性双体 ) protein, non-specific binding to DNA, most abundant. H-NS (protein H1): neutral monomeric ( 中性单 体 ), partially non-specific binding Site-specific DNA binding proteins important for organization of DNA domains (RNA polymerases, IHF etc).
D2 Chromatin Structure — Chromatin Fig. 1: The major structures in DNA compaction; DNA, the nucleosome, the 10nm "beads-on-a-string" fibre, the 30nm fibre and the metaphase chromosome. DNA compaction nucleosome 10nm "beads-on- a-string" fibre 30nm fibre metaphase chromosome DNA
D2 Chromatin Structure — Histones The major protein components of chromatin. Four families of core histone: H2A, H2B, H3 and H4, An additional non-core histone H1. Small, 10 kDa for core histones and 23 kDa for H1. Basic (rich in lysine and arginine) and tightly binds to DNA.
Histone octamer Top view Side view
D2 Chromatin Structure — Nucleosomes The nucleosome core is the basic unit of chromosome structure, consisting of a protein octamer containing two each of core histones. With 146 bp of DNA wrapped 1.8 times in a left-handed fashin around it. The wrapped of DNA into nucleosomes accounts for virually all of the negative supercoiling in eukaryotic DNA.
D2 Chromatin Structure — The role of H1 Stabilizes the point at which DNA enters and leaves the nucleosome core. linker histone H1 and H5 family C- tail of H1: stabilizes the DNA between the nucleosome cores.
D2 Chromatin Structure — Linker DNA The additional DNA required to make up the 200 bp nucleosomal repeat, ~55 bp
D2 Chromatin Structure — The 30 nm fiber Higher ordered Left-handed helix Six nucloesomes per turn
D2 Chromatin Structure — Highter order structure On the largest scale, chromosomal DNA is organized into loops of up to 100 kb in the foem of the 30nm fiber
D3 Eukaryotic Chromosomal Structure — The mitotic chromosome Centromere Telomere Mitotic chromosome at metaphase Nuclear matrix Loops of 30nm fiber Sister chromatid Chromatid
D3 Eukaryotic Chromosomal Structure — The centromere The region where two chromatids are joined. The sites of attachment to the mitotic spindle via kinetochore. Centromere DNA. Chromosomal components: ① Chromatid ② Centromere/Primary Constriction ③ Short arm ④ Long arm
D3 Eukaryotic Chromosomal Structure — Telomeres Specialized DNA sequences which form the ends of the linear DNA of the eukaryotic chromosome. Contains up to hundreds copies of a short repeated sequence (5’-TTAGGG-3’ in human). Synthesized by the enzyme telomerase (a ribonucleoprotein) independent of normal DNA replication. The telomeric DNA forms a special secondary structure to protect the chromosomal ends from degradation.
Human chromosomes (grey) capped by telomeres (white).
D3 Eukaryotic Chromosomal Structure — Interphase chromosome In interphase, the chromosomes adopt a much more diffuse structure, although the chromosomal loops remain attached to the nuclear matrix. Cannot be visualized individually.
D3 Eukaryotic Chromosomal Structure — Heterochromatin 异染色质 Highly condensed Transcriptionally inactive Can be the repeated satellite DNA close to the centromeres, and sometimes a whole chromosome (e.g. one X chromosome in mammals)
D3 Eukaryotic Chromosomal Structure — Euchromatin Euchromatin: chromatin other than heterochromatin. More diffused and not visible The region where transcription takes place Not homogenous, only a portion (~10%) euchromatin is transcriptionally active where the 30nm fiber has been dissociated to “beads on a string” structure and parts of these regions may be depleted of nucleosome.
The nucleus of a human cell showing the location of heterochromatin. Animal cells Plant cells
D3 Eukaryotic Chromosomal Structure — DNase Ⅰ hypersensitivity Active regions of chromatin, or regions where the 30nm fiber is interrupted by the binding of a specific protein to the DNA, or by ongoing transcription, are characterized by hypersensitivity to deoxyribonuclease Ⅰ (DNase Ⅰ ).
D3 Eukaryotic Chromosomal Structure — CpG methylation Methylation of C-5 in the cytosine （胞嘧啶） base of 5’- CG-3’ Occurs in mammalian cells Signaling the appropriate level of chromosomal packing at the sites of expressed genes CpG methylation is associated with transcriptionally inactive regions of chromatin Islands of unmethylated CpG are coincident with regions of DNase I hypersensitivity “Islands”: surround the promoters of housekeeping genes. Responsible for epigenetic （渐成说） and may also to RNA silencing.
D3 Eukaryotic Chromosomal Structure — Histone variants and modification The major mechanisms for the condensing and decondensing of chromatin operate directly through the histone proteins which carry out the packaging. Histones undergo posttranslational modifications which alter their interaction with DNA and nuclear proteins. The H3 and H4 histones have long tails can be covalently modified. Modifications of the tail include methylation, acetylation, phosphorylation, etc. The core of the histones (H2A and H3) can also be modified. Histone modifications act in diverse biological processes such as gene regulation, DNA repair and chromosome condensation (mitosis).
D4 Genome complexity — Noncoding DNA DNA sequence that does not code for protein or RNA, including Introns (unique sequence) in genes DNA consisting of multiple repeats, can be tandemly repeated sequences (e.g. satellite DNA) or interspersed repeats (e.g. Alu element) etc.
D4 Genome complexity — Unique sequence DNA The slowest to reassociate （复性最慢） Corresponds to coding regions of genes occurring in one or a few copies/haploid genome All the DNA in E. coli genome has a unique sequence.
D4 Genome complexity — Tandem gene clusters Tandem gene clusters: (1)moderately repetitive DNA consists of a number of types of repeated sequence. (2)genes whose products are required in unusually large quantities, e.g. there are copies of rDNA encoding 45S precursor and X100 copies of histone genes.
D4 Genome complexity — Dispersed repetitive DNA Moderately repetitive (x100- x1000 copies) Scattered throughout the genome Human Alu elements: 300bp, – copies of 80-90% identity Human L1 element Alu + L1= ~ 10% of human genome. Functions of these repetitive DNA ： largely unknown
D4 Genome complexity — Satellite DNA Highly repetitive DNA (>106), very short (2 to 20-30bp, mini- or micro-), in tandem arrays concentrated near the centromeres and forms a large part of heterochromatin. as separate band in buoyant density gradient no function found, except a possible role in kinetochore binding Minisatellite repeats are the basis of the DNA fingerprinting techniques.
D5 The flow of genetic information — The central dogma
D5 The flow of genetic information — Prokaryotic gene expression 5‘ 3‘ 5‘ DNA 3‘ Transcribed region PromoterTerminator 5‘ pop mRNA OH 3‘ AUG RBS stopAUGstop RBS Transcription RNA polymerase Proteins Ribosomes, aminoacyl-tRNAs Translation
D5 The flow of genetic information — Eukaryotic gene expression 5‘ 3‘ 5‘ DNA 3‘ Transcribed region Promoter 5‘ pop Pre-mRNA AUG Poly( A) site INTRON stop EXONS Transcription RNA polymerase Ⅱ mRNA Splicing, capping, polyadenylation RNA processing 5‘ MeGppp AUG Poly( A) tail stop Ribosomes, aminoacyl-tRNAs Translation CAP AAA…3‘ Proteins
Cytoplasm －－－ cellular organelles Mitochondrion 类囊体 Chloroplast The endoplasmic reticulum (ER) is responsible for the production of the protein and lipid components of most of the cell's organelles. 池 Golgi Apparatus 。 The Golgi is principally responsible for directing molecular traffic in the cell Cellular organelles you should further understand
Cellular organelles （ continue ） Lysomoes （溶酶体）， which contains hydrolytic enzymes 肌动蛋白 Cytoskeleton( 细胞骨架 ) The ribosome plays a key role in the synthesis of proteins. The vacuole is used only in plant cells. It is responsible for maintaining the shape and structure of the cell.
Multiple choice questions 1 ． Which of the following is common to both E. coli and eukaryotic chromosomes? A the DNA is circular. B the DNA is packaged into nucleosomes. C the DNA is contained in the nucleus. D the DNA is negatively supercoiled. 2 ． A complex of 166 bp of DNA with the histone octamer plus histone HI is known as a... A nucleosome core. B solenoid. C 30 nm fiber. D chromatosome.
3 ． In what region of the interphase chromosome does transcription take place? A the telomere. B the centromere. C euchromatin. D heterochromatin. 4 ． Which statement about CpG islands and methylation is not true? A CpG islands are particularly resistant to DNase I. B CpG methylation is responsible for the mutation of CpG to TpG in eukaryotes. C CpG islands occur around the promoters of active genes. D CpG methylation is associated with inactive chromatin.
5 ． Which of the following is an example of highly-repetitive DNA? A Alu element. B histone gene cluster. C DNA minisatellites. D dispersed repetitive DNA.