* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Cells can contain one type or a mixture of organelle genomes
Ridge (biology) wikipedia , lookup
Deoxyribozyme wikipedia , lookup
Pathogenomics wikipedia , lookup
Metagenomics wikipedia , lookup
Biology and consumer behaviour wikipedia , lookup
List of haplogroups of historic people wikipedia , lookup
Cell-free fetal DNA wikipedia , lookup
Genomic library wikipedia , lookup
Genetic engineering wikipedia , lookup
Cancer epigenetics wikipedia , lookup
No-SCAR (Scarless Cas9 Assisted Recombineering) Genome Editing wikipedia , lookup
Polycomb Group Proteins and Cancer wikipedia , lookup
DNA barcoding wikipedia , lookup
Quantitative trait locus wikipedia , lookup
Nutriepigenomics wikipedia , lookup
Vectors in gene therapy wikipedia , lookup
Genomic imprinting wikipedia , lookup
Human genome wikipedia , lookup
Genome (book) wikipedia , lookup
Gene expression profiling wikipedia , lookup
Therapeutic gene modulation wikipedia , lookup
Primary transcript wikipedia , lookup
Non-coding DNA wikipedia , lookup
Epigenetics of human development wikipedia , lookup
Designer baby wikipedia , lookup
Site-specific recombinase technology wikipedia , lookup
Genome editing wikipedia , lookup
Artificial gene synthesis wikipedia , lookup
Minimal genome wikipedia , lookup
Point mutation wikipedia , lookup
Helitron (biology) wikipedia , lookup
History of genetic engineering wikipedia , lookup
Genealogical DNA test wikipedia , lookup
Genome evolution wikipedia , lookup
Microevolution wikipedia , lookup
Oncogenomics wikipedia , lookup
Extrachromosomal DNA wikipedia , lookup
The Chromosomes of Organelles Outside the Nucleus Exhibit NonMendelian Patterns of Inheritance Outline of Chapter 15 The structure and function of mitochondrial and chloroplast genomes, including a description of their size, shape replication, and expression How genetic transmission revealed and explained non-Mendelian patterns of inheritance A comprehensive example of mutations in mitochondrial DNA that affect human health Mitochondrial and chloroplasts are organelles of energy conversion that carry their own DNA Chloroplasts – capture solar energy and store it in carbohydrates Mitochondria – release energy from nutrients and convert it to ATP Mitochondria are sites of the Krebs cycle and an electron transport chain that carries out the oxidative phophorylation of ADP to ATP Fig 15.2 Two stages by which mitochondria convert food to energy Krebs cycle Metabolize pyruvate and fatty acids Produce high-energy electron carriers NADH and FADH2 Oxydative phosphorylation Reactions that create ATP Molecular complexes I, II, III, IV form a chain that transports electrons from NADH and FADH2 to the final electron acceptor, oxygen Complex V uses the energy released by the electron transport chain to form ATP Chloroplasts are sites of photosynthesis Capture, conversion, and storage of solar energy in bonds of carbohydrates Fig. 15.3 Photosynthesis takes place in two parts Light trapping phase Solar energy is trapped and boosts electrons in chlorophyll Electrons are conveyed to electron transport systeme to convert water to oxygen and H+ Electron transport forms NADPH and drives synthsis of ATP Sugar-building phase Calvin cycle enzymes use ATP and NADPH to fix atmospheric carbon dioxide into carbohydrates Energy is stored in carbohydrate bonds The genomes of mitochondria Location mtDNA lies within matrix of the organelle in structures called nucleoids mtDNA of most cells does not reside in single location The size and gene content of mtDNA vary from organism to organism Unusually organized mtDNAs of Trypanosoma, Leishmania, Crithidia Protozoan parasites with single mitochondrial called kinetoplast mtDNA exists in one place within kinetoplast Large network of 10-25,000 minicircles 0.5 – 2.5 kb in length interlocked with 50-100 maxicircles 21-31 kb long Maxicircles contain most genes Minicircles involved in RNA editing Human mtDNA carries closely packed genes 16.5 kb in length, or 0.3% of total genome length Carries 37 genes Compact gene arrangement Fig. 15.5 a 13 encode polypeptide subunits that make up oxydative phosphorylation apparatus 22 tRNA genes 2 genes for large and small rRNAs No introns Genes abut or slightly overlap The larger yeast mtDNA contains spacers and introns Four times longer than human and other animal mtDNA Figure 15.5 b Long intergenic sequences called spacers separate genes accounting for more than half of DNA Introns form about 25% of yeast genome The 186 kb mtDNA of the liverwort carries many more genes than animals and fungi 12 electron transport genes 16 ribosomal protein genes 29 genes with unknown function Fig. 15.5 c Mitochondrial transcripts undergo RNA editing, a rare variation on the basic theme of gene expression Discovered in trypanosomes Sequence of maxicircle DNA reveals only short, recognizable gene fragments instead of whole genes RNAs in kinetoplast are same short fragments and full length RNAs kDNA encodes a precursor for each mRNA RNA editing – conversion of pre-mRNA to mature mRNA Also found in mitochondria of some plants and fungi RNA editing in trypanosomes Fig. 15.6 Translation in mitochondria shows that the genetic code is not universal The genomes of chloroplasts: the liverwort, M. polymorpha Mitochondrial and chloroplast genomes require cooperation between organelle and nuclear genomes Fig. 15.8 Origin and evolution of organelle genomes: molecular evidence Endosymbiont theory 1970s, Lynn Margulis Mitochondria and chloroplasts orginated more than a billion years ago Ancient precursors of eukaryotic cells engulfed bacteria and established symbiotic relationship Molecular evidence Both chloroplasts and mitochondria have own DNA mtDNA and cpDNA are not organized into nucleosomes by histones, similar to bacteria Mitochondrial genomes use N-formyl methionine and tRNAfmet in translation Inhibitors of bacterial translation have same effect on mitochondrial translation, but not eukaryotic cytoplasmic protein synthesis Gene transfer occurs through an RNA intermediate or movement of pieces of DNA Genes transfer between organelles and the nucleus COXII gene mtDNA genome in some plants Nuclear genome in other plants Nuclear copy lacks intron – suggests transferred by RNA intermediate Movement among organelles Plant mtDNAs carry fragments of cpDNA Nonfunctional copies of organelle DNA are found around the nuclear genomes of eukaryotes mtDNA has high rate of mutation 10 times higher than nuclear DNA Provides a tool for studying evolutionary relationships among closely related organisms maternal lineage of humans trace back to a few women who lived about 200,000 years ago Maternal inheritance only in most species Maternal inheritance of Xenopus mtDNA Fig. 15.9 Purified mtDNA from two species Hybridization only to probes from same species F1 hybrids retain only mtDNA from mother Maternal inheritance of specific genes in cpDNA Interspecific crosses tracing biochemically detectable species specific differences in chloroplast proteins Isolated Rubisco proteins in tobacco plants in which interspecific differences could be seen Progeny of controlled crosses contained version of Rubisco protein from maternal parent only A mutation in human mtDNA generates a maternally inherited neurodegenerative disease Fig. 15.10 Leber’s hereditary optic neurophathy (LHON) leads to optic nerve degeneration and blindness Substitution in mtDNA at nucleotide 11,778 Cells can contain one type or a mixture of organelle genomes Heterplasmic – cells contain a mixture of organelle genomes Mitotic products may contain one type, a mixture of types, or the second type Homoplastic – cells contain one type of organelle DNA Mitotic products contain same type, except for rare mutation Mitotic segregation produces an uneven distribution of organelle genes in heteroplasmic cells Women with heteroplasmic LHON mutation Some ova may carry few mitochondria with LHON mutation and large number of wild-type Other ova may carry mainly mitochondrial with LHON mutation and few wild-type Consequence of heteroplasmy after fertilization Some cells produce tissues with normal ATP production and others with low production If low production cells are in optic nerve, LHON results Experiments with mutants of cpDNA in Chlamydomonas reinhardtii reveal uniparental inheritance of chloroplasts Fig. 15.11 b A cross of C. reinhardtii gametes illustrates lack of segregation of cpDNA at meiosis Fig. 15.11 c Mechanisms of unipartental inheritance Differences in gamete size Degredation of organelles in male gametes of some organisms In some plants paternal organelle genomes are distributed to cells that are destined to not become part of the embryo during early development In some organisms, the zygote destroys paternal organelle after fertilization Other organisms, paternal organelles excluded from female gamete In yeast, mtDNA-encoded traits show a biparental mode of inheritance and mitotic segregation Fig. 15.13 Recombinant DNA techniques to study genetics of organelles Gene gun – biolistic transformation Fig. 15.14 Small (1mm) metal beads with DNA are shot at cells Rarely, DNA passes through cell wall and enters nucleus Used to transform cells E.g., GFP constructs can be used as selectable markers to identify transformants How mutations in mtDNA affect human health Individuals with certain rare diseases of the nervous system are heteroplasmic MERRF, myoclonic epilepsy and ragged red fiber disease Fig. 15.15 a Uncontrolled jerking, muscle weakness, deafness, heart problems, kidney problems, progressive dementia Maternal inheritance of MRRF Fig. 15.15 b Proportion of mutant mtDNA and tissue in which they reside influence phenotype Fig. 15.16 Mitochondrial inheritance in identical twins Mitochondrial genomes not same in twins but nuclear genomes are identical Symptoms of neurodegenerative diseases or other mutations may manifest in one twin, but not other In heteroplasmic mother, chance of phenotype depends on both partitioning of mutant mtDNA after fertilization, and tissue that receive mutation during development mtDNA mutations and aging Hypothesis: Accumulation of mutations in mtDNA over lifetime and biased replication of deleted mtDNA result in age-related decline in oxidative phosphorylation Evidence: Deleterious mtDNA mutations early in life diminish ATP production Decreases in cytochrome c oxidase in hearts from autopsies (gene encoded in mtDNA) Rate of deletions increases with age Alzheimer’s individuals have abnormally low energy metabolism