Origin of mitochondria and chloroplasts Both mitochondria and
Origin of mitochondria and chloroplasts: Both mitochondria and chloroplasts are believed to be derived from endosymbiotic bacteria. Endosymbiotic bacteria = free-living prokaryotes that invaded ancestral eukaryotic cells and established a mutually beneficial relationship. Many required mitochondria and chloroplast proteins also are coded by nuclear genes. numt = nuclear mt. DNA (mt. DNA transposed to the nucleus)
Time-line of life on earth Origin of life Oxygen appears Multicellular Cambrian life explosion First land plants First vertebrates 3800 MY 2500 MY 1000 MY 530 MY 410 MY
Origin of Eukaryotic Diversity
Organelle genomes Genome Size & Organization Plant plastid 150 kb circle Plant mitochondria 150 – 2000 kb multipartite Human mitochondria 17 kb circle saccharomyces mitochondria 75 kb circle Encode only a subset of genes required to elaborate a functional organelle r. RNAs, t. RNAs, ribosomal proteins, membrane-associated respiratory or photosynthetic components Other components encoded by nuclear genome, translated in the cytosol and imported into the organelle 10% of nuclear genes devoted to mitochondrial function; 15% of nuclear genes devoted to plastid function Associated with proteins and organized into structures called nucleoids (not the same as nucleosomes found in nuclear chromatin)
Eukaryotes Organelle-Genomes • Ribosomal RNA sequences suggests that plant plastids share common ancestor with modern Cyanobacteria such as Synechococcus lividus • Mt-r. RNA share greatest homology with members of alpha -group of proteobacteria which includes intracellular parasites (Agrobacterium, Rhizobium)
• Mitochondria make up some 80% of the volume of the cone cell photoreceptors of the eye and 40% of the volume of heart muscle cells.
Mitochondria are essential for oxidative phosphorylation (make ATP)
Mitochondria are essential for oxidative phosphorylation (make ATP) • • However they play important roles in most other metabolic functions of the cell: * Pyrimidine synthesis * Heme synthesis (red blood precursor cells) * Amonia detoxification (liver) * Cholesterol metabolism * Sex hormone synthesis * Free radical production and detoxification * Apoptosis
• In fact out of the 3000 genes required to make a mitochondrion only 100 are concerned with making ATP.
(human: 2 -10 mt. DNA per mitochondrion)
Chloroplast DNA-Microscopic Image • Electron microscopic image of a circular DNA molecule isolated from a soybean chloroplast (a ct. DNA). N. M. Chu, K. K. Tewari, 1982 1 µm
Fig. 15. 2, mt. DNA replication
Transcription of the mt. DNA genome: • m. RNAs from the mt. DNA are synthesized and translated in the mitochondria. • Gene products encoded by nuclear genes are transported from the cytoplasm to the mitochondria. • Mammalian mt. DNA is unusual as it is transcribed as a single large RNA molecule and then cleaved to produce m. RNAs, t. RNAs, and r. RNAs before they are processed. • Most mt. DNA genes are separated by t. RNAs that signal transcription termination.
No coded stop codons
Mitochondrial code Universal code
Wobble rules: G C A U U/C G U A/G 32 t. RNAs required
More Wobble in mitochondria 22 t. RNAs required
Fig. 15. 3, Physical map of the human mt. DNA
Mitochondrial DNA mutations in human genetic disease (Wallace Sci. Amer. 277: 40)
Examples of maternally inherited human mt. DNA defects: • Leber’s hereditary optic neuropathy (LHON), OMIM-535000 • • • Kearns-Sayre Syndrome, OMIM-530000 • • • Midlife adult blindness from optic nerve degeneration. Mutations in ND 1, ND 2, ND 4, ND 5, ND 6, cyt b, CO II, and ATPase 6 inhibit electron transport chain. Paralysis eye muscles, accumulation of pigment and degeneration of the retina, and heart disease. Deletion of mt. DNA t. RNAs. Myoclonic epilepsy & ragged-red fiber disease (MERRF), OMIM 545000 • • Spasms and abnormal tissues, accumulation of lactic acid in the blood, and uncoordinated movement. Nucleotoide substitution in the mt. DNA lysine t. RNA. Most individuals with mt. DNA disorders possess a mix of normal and mutant mt. DNA, therefore severity of diseases varies.
Mitochondrial DNA mutations in human genetic disease (Wallace Sci. Amer. 277: 40)
Mitochondrial DNA polymorphisms track human migrations (Wallace Sci. Amer. 277: 40) All humans descend from a small group of Africans This group originated in central Africa ~200, 000 years ago The founding group was small (102 -104 people) Descendants of this group replaced all other hominids everywhere in the world
Maternal effect: Some maternal phenotypes are produced by the nuclear genome rather than the mt. DNA/cp. DNA genomes. • Proteins or m. RNA (maternal factors) deposited in the oocyte prior to fertilization. • Genes for maternal factors occur on nuclear chromosomes; no mt. DNA is involved • e. g. , shell coiling in the snail Limnaea peregra. • Determined by a pair of nuclear alleles; D produces dextral (right-handed) coiling, d produces sinistral (left-handed) coiling. • Shell coiling always is determined by the maternal genotype, not the alleles that the progeny carry or maternal phenotype. • If coiling were controlled by an extranuclear gene, progeny would always have the same phenotype as the mother. • Cause-mother snail deposits products in the egg that regulate orientation of the mitotic spindle and direction of cell cleavage.
Fig. 15. 14 dextral sinistral *****dextral *****
Plant Cell
Higher Plant Chloroplasts
Fig. 15. 5 cp. DNA of rice
Examples of non-Mendelian inheritance: • Variegated-shoot phenotypes in four o’clocks Mixed chloroplasts White/green Mutant chloroplast White non-photosynthetic Normal chloroplast Green photosynthetic Fig. 15. 6 b
Fig. 15. 7 Chloroplasts are inherited via the seed cytoplasm 3 types of eggs (female): Normal Mutant Mixed Assumption: Pollen (male) contributes no information
The search for new antimalarial drugs • Malaria is one of the leading causes of morbidity and mortality in the tropics. • 300 to 500 million estimated clinical cases and 1. 5 million to 2. 7 million deaths per year. • Nearly all fatal cases are caused by Plasmodium falciparum. • The parasite's resistance to conventional antimalarial drugs such as chloroquine is growing at an alarming rate.
• P. falciparum has a plastidlike organelle, called the apicoplast, acquired by endosymbiosis of an alga. Jomaa et al. (1999) Apicoplast contains enzymes found in plant and bacterial, but not animal metabolic pathways. • Potential target for antimalerial drugs: DOXP reductoisomerase
Endosymbiosis
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