Evolution of Genomes Evolution of the eukaryotic cell Human evolution

Endosymbiotic Events Mitochondria originated from Proteobacteria Mitochondria originated from Proteobacteria Chloroplasts originated from Cyanobacteria Chloroplasts originated from Cyanobacteria Where did the nucleus originate from? Where did the nucleus originate from?

Genomic Study of Endosymbiosis Takao Shinozawa’s group in Japan compared orthologs between yeast an either eubacteria or archaea. Takao Shinozawa’s group in Japan compared orthologs between yeast an either eubacteria or archaea. E-values are represented as -log E (the larger the # the better E-value). E-values are represented as -log E (the larger the # the better E-value). The bit scores get larger as the E-values decrease, resulting in a lower # of hits (lines have - slope) The bit scores get larger as the E-values decrease, resulting in a lower # of hits (lines have - slope) A t-statistic test was performed comparing data from the two domains. A t-statistic test was performed comparing data from the two domains. A t-stat of > indicates Archaeal origin, while a value of indicates Archaeal origin, while a value of < indicates Eubacteria.

Mitochondrial Genes Originated from Eubacteria t-stats are < for most E-values

Nuclear Genes Originated from Archaebacteria t-stats are > for most E-values

Cytoplasmic Genes Show No Distinct Origin t-stats are sometimes > and sometimes <

t-statistics In the mitochondrial example, the values at an E- value of were 12, 15, 19, 21,24 & 27 for Archaea and 65, 66, 68, 73, 75, 80, 81, 82 & 93 for Eubacteria. We then determine the sample size (n), the mean (y), and the standard deviation (s) for each. In the mitochondrial example, the values at an E- value of were 12, 15, 19, 21,24 & 27 for Archaea and 65, 66, 68, 73, 75, 80, 81, 82 & 93 for Eubacteria. We then determine the sample size (n), the mean (y), and the standard deviation (s) for each. The standard deviations are then pooled using: The standard deviations are then pooled using: s p = sq rt [((n 1 - 1) s (n 2 -1) s 2 2 )/(n 1 + n 2 -2)] The t-statistic is then determined by: The t-statistic is then determined by: t = (y 1 - y 2 )/(s p * sq rt [1/ n 1 + 1/ n 2 ] In this case, t < (Eubacterial origin)

Existing organisms may provide information on “missing-links” between bacteria and eukaryotes Buchnera M. leprae

Buchnera All animals, with the exception of aphids, excrete toxic nitrogenous waste All animals, with the exception of aphids, excrete toxic nitrogenous waste Aphids have large cells in their abdomens called bacteriocytes Aphids have large cells in their abdomens called bacteriocytes Bacteria called Buchnera inhabit this organ Bacteria called Buchnera inhabit this organ Neither organism can reproduce without the other Neither organism can reproduce without the other Their symbiotic relationship is thought to date back 225 million years Their symbiotic relationship is thought to date back 225 million years

The Buchnera Genome At 640,681 bp, it is the 2nd smallest sequenced At 640,681 bp, it is the 2nd smallest sequenced Contains 583 genes Contains 583 genes 500 are very similar to E. coli, 79 are related to other bacterial, only 4 are unique to Buchnera 500 are very similar to E. coli, 79 are related to other bacterial, only 4 are unique to Buchnera Many genes which are non-essential to the symbiotic relationship have been lost over time Many genes which are non-essential to the symbiotic relationship have been lost over time Buchnera can only synthesize amino acids which aphids are unable to produce Buchnera can only synthesize amino acids which aphids are unable to produce

Types of genes which Buchnera lack DNA repair enzymes DNA repair enzymes cell wall synthesizing enzymes cell wall synthesizing enzymes enzymes involved in phospholipid synthesis enzymes involved in phospholipid synthesis components of signaling pathways components of signaling pathways Types of genes which Buchnera have certain amino acid synthesis certain amino acid synthesis certain vitamin synthesis certain vitamin synthesis ATP synthase ATP synthase ETC ETC

Buchnera acts as if it is evolving into a new organelle It uses glutamine as a substrate to make essential amino acids, hence no nitrogenous waste is produced It uses glutamine as a substrate to make essential amino acids, hence no nitrogenous waste is produced Someday it may be completely engulfed by cells as an “aminoacid-plast” Someday it may be completely engulfed by cells as an “aminoacid-plast”

Mycobacterium leprae The causative agent of leprosy The causative agent of leprosy Lives inside macrophages and myelin- producing Schwann cells Lives inside macrophages and myelin- producing Schwann cells Still infects many people, mostly in 3rd world countries Unable to be cultured in the laboratory Still infects many people, mostly in 3rd world countries Unable to be cultured in the laboratory Must be grown in the nine-banded armadillo Must be grown in the nine-banded armadillo The bacterium divides once every 14 days The bacterium divides once every 14 days

The M. leprae Genome Contains 3.3 million bp (compared to the 4.4 million of M. tuberculosis) Contains 3.3 million bp (compared to the 4.4 million of M. tuberculosis) Encodes 1,600 proteins (compared to 4,000) Encodes 1,600 proteins (compared to 4,000) Only 50% of genome codes for proteins Only 50% of genome codes for proteins The rest is pseudogenes (1100 in number) The rest is pseudogenes (1100 in number) Other genes appear to have been replaced by orthologs Other genes appear to have been replaced by orthologs

Pseudogenes in M. leprae

M. leprae vs. M. tuberculosis certain membrane lipids certain membrane lipids genes involved in TCA and glycolysis genes involved in TCA and glycolysis malic enzyme malic enzyme methionine synthesis methionine synthesis Genes lacking in M. leprae

Slow-growing organisms which have lost many genes but can still live independently represent one more step in the production of an organelle

Human Evolution 3000 bp of nuclear sequence was used to create phylogenetic trees. Humans are closely related to the great apes. The base of the mammalian tree is a Tree shrew.

Bootstrap Analysis How do we know that a tree is right? How do we know that a tree is right? 1) use different methods to create the tree: distance- based, maximum parsimony, etc. 2) use bootstrap analysis Bootstrapping repeats the tree-building process thousands of times using different subsequences Bootstrapping repeats the tree-building process thousands of times using different subsequences The percent of times that a branch point agrees in the various replicates becomes its bootstrap value The percent of times that a branch point agrees in the various replicates becomes its bootstrap value A bootstrap value > 70 is considered reliable A bootstrap value > 70 is considered reliable

How much diversity is there among groups of primates? MRCA for humans was 540,000 years ago MRCA for humans was 540,000 years ago MRCA for gorilla was 1.2 million years ago MRCA for gorilla was 1.2 million years ago MRCA for chimps was 1.9 m years ago MRCA for chimps was 1.9 m years ago MRCA for orangutans was 2.1 m years ago MRCA for orangutans was 2.1 m years ago Humans were seen to have less diversity than any of the great apes since Neanderthals have become extinct. 10,000 bp of non-coding DNA from X chromosomes of various primates was compared. The MRCA (Most Recent Common Ancestor) was determined for each.

Where and when did modern humans evolve? One theory: “recent Africa hypothesis” predicts African origin 100, ,000 years ago. One theory: “recent Africa hypothesis” predicts African origin 100, ,000 years ago. Another theory: “multiregional hypothesis” predicts a gradual evolution at sites around the world. Another theory: “multiregional hypothesis” predicts a gradual evolution at sites around the world. Genomic data from mitochondria (16,500 bp) were compared between people from diverse locations. A phylogenetic tree reveals how long it has been since African and non-African populations converged. The MRCAs for various populations can be determined

The origin and dispersal of humans MRCA for Africans and non-Africans was 52,000 +/- 27,500 years MRCA for Africans and non-Africans was 52,000 +/- 27,500 years MRCA for all modern humans was 171,500 +/- 50,000 years MRCA for all modern humans was 171,500 +/- 50,000 years These data support the recent Africa hypothesis