tenth edition 26 biology/unit 8/unit 8/chap 26... · campbell biology reece • urry • cain •...
TRANSCRIPT
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CAMPBELL
BIOLOGY Reece • Urry • Cain • Wasserman • Minorsky • Jackson
© 2014 Pearson Education, Inc.
TENTH EDITION
26 Phylogeny and the Tree of Life
Lecture Presentation by Nicole Tunbridge and Kathleen Fitzpatrick
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Investigating the Tree of Life
Legless lizards have evolved independently in several different groups
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Figure 26.1
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Phylogeny is the evolutionary history of a species or group of related species
For example, a phylogeny shows that legless lizards and snakes evolved from different lineages of legged lizards
The discipline of systematics classifies organisms and determines their evolutionary relationships
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Figure 26.2
ANCESTRAL LIZARD (with limbs)
Geckos
No limbs Snakes
Iguanas
Monitor lizard
Eastern glass lizard No limbs
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Concept 26.1: Phylogenies show evolutionary relationships Taxonomy is the scientific discipline concerned
with classifying and naming organisms
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Binomial Nomenclature
In the 18th century, Carolus Linnaeus published a system of taxonomy based on resemblances
Two key features of his system remain useful today: two-part names for species and hierarchical classification
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The two-part scientific name of a species is called a binomial
The first part of the name is the genus
The second part, called the specific epithet, is unique for each species within the genus
The first letter of the genus is capitalized, and the entire species name is italicized
Both parts together name the species (not the specific epithet alone)
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Hierarchical Classification
Linnaeus introduced a system for grouping species in increasingly inclusive categories
The taxonomic groups from broad to narrow are domain, kingdom, phylum, class, order, family, genus, and species
A taxonomic unit at any level of hierarchy is called a taxon
The broader taxa are not comparable between lineages
For example, an order of snails has less genetic diversity than an order of mammals
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Figure 26.3 Cell division error Species:
Panthera pardus
Genus: Panthera Family: Felidae
Order: Carnivora
Class: Mammalia
Phylum: Chordata
Domain: Archaea
Kingdom: Animalia
Domain: Eukarya
Domain: Bacteria
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Animation: Classification Schemes
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Linking Classification and Phylogeny
The evolutionary history of a group of organisms can be represented in a branching phylogenetic tree
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Figure 26.4 Order Family Genus Species
Panthera pardus (leopard)
Taxidea taxus (American badger) Lutra lutra (European otter)
Canis latrans (coyote)
Canis lupus (gray wolf)
Panthera Taxidea
Lutra
Felidae M
ustelidae
Carnivora
Canis
Canidae
2
1
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Linnaean classification and phylogeny can differ from each other
Systematists have proposed a classification system that would recognize only groups that include a common ancestor and all its descendants
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A phylogenetic tree represents a hypothesis about evolutionary relationships
Each branch point represents the divergence of two species
Tree branches can be rotated around a branch point without changing the evolutionary relationships
Sister taxa are groups that share an immediate common ancestor
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A rooted tree includes a branch to represent the last common ancestor of all taxa in the tree
A basal taxon diverges early in the history of a group and originates near the common ancestor of the group
A polytomy is a branch from which more than two groups emerge
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Figure 26.5
1
2
3
4
5
Branch point: where lineages diverge
ANCESTRAL LINEAGE
This branch point represents the common ancestor of taxa A–G.
This branch point forms a polytomy: an unresolved pattern of divergence.
Taxon A
Taxon B
Taxon C
Taxon D
Taxon E
Taxon F
Taxon G
Sister taxa
Basal taxon
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What We Can and Cannot Learn from Phylogenetic Trees Phylogenetic trees show patterns of descent, not
phenotypic similarity
Phylogenetic trees do not indicate when species evolved or how much change occurred in a lineage
It should not be assumed that a taxon evolved from the taxon next to it
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Applying Phylogenies
Phylogeny provides important information about similar characteristics in closely related species
A phylogeny was used to identify the species of whale from which “whale meat” originated
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Figure 26.6
Results Minke (Southern Hemisphere) Unknowns #1a, 2, 3, 4, 5, 6, 7, 8 Minke (North Atlantic)
Humpback
Blue
Unknown #9
Unknown #1b
Unknowns #10, 11, 12, 13 Fin
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Concept 26.2: Phylogenies are inferred from morphological and molecular data To infer phylogenies, systematists gather
information about morphologies, genes, and biochemistry of living organisms
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Morphological and Molecular Homologies
Phenotypic and genetic similarities due to shared ancestry are called homologies
Organisms with similar morphologies or DNA sequences are likely to be more closely related than organisms with different structures or sequences
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Sorting Homology from Analogy
When constructing a phylogeny, systematists need to distinguish whether a similarity is the result of homology or analogy
Homology is similarity due to shared ancestry
Analogy is similarity due to convergent evolution
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Convergent evolution occurs when similar environmental pressures and natural selection produce similar (analogous) adaptations in organisms from different evolutionary lineages
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Figure 26.7
Australian marsupial “mole”
North American eutherian mole
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Bat and bird wings are homologous as forelimbs, but analogous as functional wings
Analogous structures or molecular sequences that evolved independently are also called homoplasies
Homology can be distinguished from analogy by comparing fossil evidence and the degree of complexity
The more elements that are similar in two complex structures, the more likely it is that they are homologous
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Evaluating Molecular Homologies
Systematists use computer programs and mathematical tools when analyzing comparable DNA segments from different organisms
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Figure 26.8-1
1 C A C C A T G T A C C G
2 C A C C A T G T A C C G
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Figure 26.8-2 Cell division error
1
2
C A C C A T
C A C C A T G T A C C G
G T A C C G
T G A Insertion
Deletion
1 C A C C A T G T A C C G
2 C A C C A T G T A C C G
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Figure 26.8-3 Cell division error
1
2 C C A T G T A C A G T A C C G
T A C C G C A C C A T
1
2
C A C C A T
C A C C A T G T A C C G
G T A C C G
T G A Insertion
Deletion
1 C A C C A T G T A C C G
2 C A C C A T G T A C C G
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Figure 26.8-4 Cell division error
1 C C A T
C C A T 2 G T A C A
C A
G T A C C G
T A C C G
1
2 C C A T G T A C A G T A C C G
T A C C G C A C C A T
1
2
C A C C A T
C A C C A T G T A C C G
G T A C C G
T G A Insertion
Deletion
1 C A C C A T G T A C C G
2 C A C C A T G T A C C G
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It is also important to distinguish homology from analogy in molecular similarities
Mathematical tools help to identify molecular homoplasies, or coincidences
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Figure 26.9
A C G G A T A G T C C A C T A G G C A C T A
C A T C C G A C A G G T C T T T G A C T A G
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Concept 26.3: Shared characters are used to construct phylogenetic trees Once homologous characters have been
identified, they can be used to infer a phylogeny
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Cladistics
Cladistics groups organisms by common descent
A clade is a group of species that includes an ancestral species and all its descendants
Clades can be nested in larger clades, but not all groupings of organisms qualify as clades
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A valid clade is monophyletic, signifying that it consists of the ancestor species and all its descendants
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Figure 26.10
(a) Monophyletic group (clade) (b) Paraphyletic group (c) Polyphyletic group
1
2
3
A
B
C
D
E
F
G
A
B
C
D
E
F
G
A
B
C
D
E
F
G
Group I
Group II
Group III
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Figure 26.10a
(a) Monophyletic group (clade)
1
A
B
C
D
E
F
G
Group I
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Figure 26.10b
(b) Paraphyletic group
2
A
B
C
D
E
F
G
Group II
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Figure 26.10c
(c) Polyphyletic group
3
A
B
C
D
E
F
G
Group III
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A paraphyletic grouping consists of an ancestral species and some, but not all, of the descendants
A polyphyletic grouping includes distantly related species but does not include their most recent common ancestor
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Polyphyletic groups are distinguished from paraphyletic groups by the fact that they do not include the most recent common ancestor
Biologists avoid defining polyphyletic groups and instead reclassify organisms if evidence suggests they are polyphyletic
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Figure 26.11
Common ancestor of even-toed ungulates
Paraphyletic group
Polyphyletic group
Other even-toed ungulates
Hippopotamuses
Cetaceans
Seals
Bears
Other carnivores
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Shared Ancestral and Shared Derived Characters In comparison with its ancestor, an organism has
both shared and different characteristics
A shared ancestral character is a character that originated in an ancestor of the taxon
A shared derived character is an evolutionary novelty unique to a particular clade
A character can be both ancestral and derived, depending on the context
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Inferring Phylogenies Using Derived Characters
When inferring evolutionary relationships, it is useful to know in which clade a shared derived character first appeared
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Figure 26.12
Lancelet (outgroup)
Lamprey
Bass
Frog
Turtle
Leopard Hair
Amnion
(b) Phylogenetic tree
Four walking legs
Hinged jaws
Vertebral column
Leop
ard
Turt
le
Frog
Bas
s
Lam
prey
Lanc
elet
(o
utgr
oup)
TAXA
Vertebral column
(backbone) Hinged jaws
Four walking legs
Amnion
Hair
CH
AR
AC
TER
S
(a) Character table
0 0 0 0 0
0 0 0 0
0 0 0
0 0
0 1 1 1 1 1
1 1 1 1
1 1 1
1 1
1
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Figure 26.12a
Character table (a)
Hair
Amnion
Four walking legs
Hinged jaws
Vertebral column
(backbone)
0 0 0 0 0
1 1 1 1 1
1 1 1 1
1 1 1
1 1
1
0 0 0 0
0 0 0
0 0
0
CH
AR
AC
TER
S
Lanc
elet
(o
utgr
oup)
Lam
prey
Bas
s
Frog
Turt
le
Leop
ard
TAXA
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Figure 26.12b
Lancelet (outgroup)
Lamprey
Bass
Frog
Turtle
Leopard Hair
Amnion
(b) Phylogenetic tree
Four walking legs
Hinged jaws
Vertebral column
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An outgroup is a species or group of species that is closely related to the ingroup, the various species being studied
The outgroup is a group that has diverged before the ingroup
Systematists compare each ingroup species with the outgroup to differentiate between shared derived and shared ancestral characteristics
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Characters shared by the outgroup and ingroup are ancestral characters that predate the divergence of both groups from a common ancestor
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Phylogenetic Trees with Proportional Branch Lengths In some trees, the length of a branch can reflect
the number of genetic changes that have taken place in a particular DNA sequence in that lineage
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Figure 26.13
Drosophila
Lancelet
Zebrafish
Frog
Chicken
Human
Mouse
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In other trees, branch length can represent chronological time, and branching points can be determined from the fossil record
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Figure 26.14
Drosophila
Lancelet
Zebrafish
Frog
Chicken
Human
Mouse
PALEOZOIC MESOZOIC 542 251 65.5 Present
Millions of years ago
CENO- ZOIC
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Maximum Parsimony and Maximum Likelihood
Systematists can never be sure of finding the best tree in a large data set
They narrow possibilities by applying the principles of maximum parsimony and maximum likelihood
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Maximum parsimony assumes that the tree that requires the fewest evolutionary events (appearances of shared derived characters) is the most likely
The principle of maximum likelihood states that, given certain rules about how DNA changes over time, a tree can be found that reflects the most likely sequence of evolutionary events
Computer programs are used to search for trees that are parsimonious and likely
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Figure 26.15
Technique
Species I Species II Species III
Three phylogenetic hypotheses: I
II
III
III
II
I III
II
I
I
III
II
3/A 2/T
3/A 4/C
I
III
II
I
III
II
I
III
II
Results
1/C
1/C
1/C I
III
II
I
III
II 1/C
1/C I
III
II
4/C 3/A
2/T
3/A 2/T
2/T 3/A
4/C
4/C 2/T
4/C
I
III
II
6 events 7 events 7 events
Species I
Species II
Species III Ancestral sequence
C
C
A
A G
G
T
T
T
T
T T
C A
C
A
1 2 4 3 Site
1
2
4
3
I
III
II
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Figure 26.15a
Technique
Species I Species II Species III
Three phylogenetic hypotheses: I
II
III
I
II
III
I
II
III 1
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Figure 26.15b
Technique
Species I 1 2 2 3 4
Species II
Species III Ancestral sequence
C
C
A
A
T
T
G
G
A
T
A
T
C
T
C
T
Site
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Figure 26.15c
I 3 1/C
4
Technique
II
III
I
II
III
1/C
1/C 1/C
1/C I
II
III
I 3/A
II
III
2/T
4/C
3/A 4/C
I
II
III
2/T 3/A
4/C
4/C 2/T
4/C 3/A
2/T
2/T 3/A I
II
III
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Figure 26.15d
I
II
III
I
II
III
I
II
III Results
6 events 7 events 7 events
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Phylogenetic Trees as Hypotheses
The best hypotheses for phylogenetic trees fit the most data: morphological, molecular, and fossil
Phylogenetic bracketing allows us to predict features of an ancestor from features of its descendants
For example, phylogenetic bracketing allows us to infer characteristics of dinosaurs
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Figure 26.16
Lizards and snakes
Crocodilians
Ornithischian dinosaurs
Saurischian dinosaurs
Birds
Common ancestor of crocodilians, dinosaurs, and birds
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Birds and crocodiles share several features: four-chambered hearts, song, nest building, and brooding
These characteristics likely evolved in a common ancestor and were shared by all of its descendants, including dinosaurs
The fossil record supports nest building and brooding in dinosaurs
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Figure 26.17
Front limb
Hind limb
Eggs
Fossil remains of Oviraptor and eggs
(a) Artist’s reconstruction of the dinosaur’s posture based on the fossil findings
(b)
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Figure 26.17a
Front limb
Hind limb
Eggs
Fossil remains of Oviraptor and eggs
(a)
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Figure 26.17b
Artist’s reconstruction of the dinosaur’s posture based on the fossil findings
(b)
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Animation: The Geologic Record
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Concept 26.4: An organism’s evolutionary history is documented in its genome Comparing nucleic acids or other molecules to
infer relatedness is a valuable approach for tracing organisms’ evolutionary history
DNA that codes for rRNA changes relatively slowly and is useful for investigating branching points hundreds of millions of years ago
mtDNA evolves rapidly and can be used to explore recent evolutionary events
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Gene Duplications and Gene Families
Gene duplication increases the number of genes in the genome, providing more opportunities for evolutionary changes
Repeated gene duplications result in gene families
Like homologous genes, duplicated genes can be traced to a common ancestor
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Orthologous genes are found in a single copy in the genome and are homologous between species
They can diverge only after speciation occurs
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Figure 26.18
(a) Formation of orthologous genes: a product of speciation
Ancestral gene
Ancestral species
Speciation with divergence of gene
Orthologous genes Species A Species B
Paralogous genes Species C after many generations
Gene duplication and divergence
Species C
Ancestral gene
Formation of paralogous genes: within a species
(b)
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Figure 26.18a Cell division error
(a) Formation of orthologous genes: a product of speciation
Ancestral gene
Ancestral species
Speciation with divergence of gene
Orthologous genes Species A Species B
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Figure 26.18b Cell division error
Paralogous genes Species C after many generations
Gene duplication and divergence
Species C
Ancestral gene
Formation of paralogous genes: within a species
(b)
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Paralogous genes result from gene duplication, so are found in more than one copy in the genome
They can diverge within the clade that carries them and often evolve new functions
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Genome Evolution
Orthologous genes are widespread and extend across many widely varied species
For example, humans and mice diverged about 65 million years ago, and 99% of our genes are orthologous
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Gene number and the complexity of an organism are not strongly linked
For example, humans have only four times as many genes as yeast, a single-celled eukaryote
Genes in complex organisms appear to be very versatile, and each gene can encode multiple proteins that perform many different functions
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Concept 26.5: Molecular clocks help track evolutionary time To extend phylogenies beyond the fossil record,
we must make an assumption about how molecular change occurs over time
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Molecular Clocks
A molecular clock uses constant rates of evolution in some genes to estimate the absolute time of evolutionary change
In orthologous genes, nucleotide substitutions are assumed to be proportional to the time since they last shared a common ancestor
In paralogous genes, nucleotide substitutions are proportional to the time since the genes became duplicated
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Molecular clocks are calibrated against branches whose dates are known from the fossil record
Individual genes vary in how clocklike they are
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Figure 26.19
90
60
30
0 0 30 90 60 120
Divergence time (millions of years)
Num
ber o
f mut
atio
ns
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Differences in Clock Speed
If most of the evolutionary change in genes and proteins has no effect on fitness then the rate of molecular change should be regular like a clock
Differences in clock rate for different genes are a function of the importance of the gene and how critical the specific amino acid is to protein function
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Potential Problems with Molecular Clocks
The molecular clock does not run as smoothly as expected if mutations were neutral
Irregularities result from natural selection in which some DNA changes are favored over others
Estimates of evolutionary divergences older than the fossil record have a high degree of uncertainty
The use of multiple genes or genes that evolved in different taxa may improve estimates
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Applying a Molecular Clock: Dating the Origin of HIV Phylogenetic analysis shows that HIV is
descended from viruses that infect chimpanzees and other primates
HIV spread to humans more than once
Comparison of HIV samples shows that the virus evolved in a very clocklike way
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Application of a molecular clock to one strain of HIV suggests that that strain spread to humans during the 1930s
A more advanced molecular clock approach estimated the first spread to humans around 1910
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Figure 26.20 Cell division error
0.20
Inde
x of
bas
e ch
ange
s be
twee
n H
IV g
ene
sequ
ence
s 0.15
0.10
0.05
0 1900 1920 1940 1960 1980 2000
Year
Range
HIV
Adjusted best-fit line (accounts for uncertain dates of HIV sequences)
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Concept 26.6: Our understanding of the tree of life continues to change based on new data Recently, we have gained insight into the very
deepest branches of the tree of life through molecular systematics
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From Two Kingdoms to Three Domains
Early taxonomists classified all species as either plants or animals
Later, five kingdoms were recognized: Monera (prokaryotes), Protista, Plantae, Fungi, and Animalia
More recently, the three-domain system has been adopted: Bacteria, Archaea, and Eukarya
The three-domain system is supported by data from many sequenced genomes
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Figure 26.21 Cell division error
Euglenozoans
Forams
Diatoms
Ciliates
Red algae
Green algae
Land plants
Fungi
Animals
Amoebas
Nanoarchaeotes
Methanogens
Thermophiles
Proteobacteria
(Mitochondria)*
Chlamydias
Spirochetes Gram-positive bacteria Cyanobacteria (Chloroplasts)*
Dom
ain Bacteria
Dom
ain A
rchaea D
omain Eukarya
COMMON ANCESTOR OF ALL LIFE
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Figure 26.21a
Euglenozoans
Forams Diatoms
Ciliates
Red algae
Green algae
Land plants
Fungi
Animals
Amoebas
Dom
ain Eukarya
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Figure 26.21b
Nanoarchaeotes
Methanogens
Thermophiles
Dom
ain A
rchaea
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Figure 26.21c
Proteobacteria
(Mitochondria)*
Chlamydias
Spirochetes Gram-positive bacteria Cyanobacteria (Chloroplasts)*
Dom
ain Bacteria
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The Important Role of Horizontal Gene Transfer
The tree of life suggests that eukaryotes and archaea are more closely related to each other than to bacteria
The tree of life is based largely on rRNA genes; however, some other genes reveal different relationships
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There have been substantial interchanges of genes between organisms in different domains
Horizontal gene transfer is the movement of genes from one genome to another
Horizontal gene transfer occurs by exchange of transposable elements and plasmids, viral infection, and fusion of organisms
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Disparities between gene trees can be explained by the occurrence of horizontal gene transfer
Horizontal gene transfer has played a key role in the evolution of both prokaryotes and eukaryotes
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Figure 26.22
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Some biologists argue that horizontal gene transfer was so common that the early history of life should be represented as a tangled network of connected branches
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Figure 26.23
Ancestral cell populations
Proteobacteria
Cyanobacteria
Thermophiles
Methanogens
Dom
ain Eukarya D
omain
Archaea
Dom
ain Bactera
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Figure 26.23a
Ancestral cell populations
Dom
ain Eukarya
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Figure 26.23b
Ancestral cell populations
Methanogens
Thermophiles
Cyanobacteria
Proteobacteria
Dom
ain Bacteria
Dom
ain A
rchaea
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Figure 26.UN01
A
B
C
D
B
A
B
C
D
D
C
B
A
(a) (b) (c)
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Figure 26.UN02a
Organism Alignment of Amino Acid Sequences
Acyrthosiphod (aphid) Ustilago (fungus) Gibberalla (fungus) Staphylococcus (bacterium) Pantoea (bacterium) Arabidopsis (plant) WDAVVIGGGH
KRTFVIGAGF MKIAVIGAGV KSVIVIGAGV KKVVIIGAGA IKIIIIGSGV GGTAAAARLS
GGTALAARLG GGVSTAARLA TGLAAAARIA GGLALAIRLQ NGLTAAAYLA
KKGFQVEVYE RRGYSVTVLE KAGFKVTILE SQGHEVTIFE AAGIATTVLE RGGLSVAVLE
KNSYNGGRCS KNSFGGGRCS KNDFTGGRCS KNNNVGGRMN QHDKPGGRAY RRHVIGGAAV
IIR-HNGHRF LIH-HDGHRW LIH-NDGHRF QLK-KDGFTF VWQ-DQGFTF TEEIVPGFKF
DQGPSL--YL DQGPSL--YL DQGPSL--LL DMGPTI--VM DAGPTV--IT SRCSYLQGLL
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Figure 26.UN02b
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Figure 26.UN03
Taxon A
Taxon B
Taxon C
Taxon D
Taxon E
Taxon F
Taxon G
Polytomy
Most recent common ancestor
Branch point
Sister taxa
Basal taxon
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Figure 26.UN04
Monophyletic group
Paraphyletic group
Polyphyletic group
A
B
C
D
E
F
G
A
B
C
D
E
F
G
A
B
C
D
E
F
G
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Figure 26.UN05
Salamander
Lizard
Goat
Human
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Figure 26.UN06
Character
(1)
(2)
(3)
(4)
(5)
(6)
Backbone
Hinged jaw
Four limbs
Amnion
Milk
Dorsal fin
*Although adult dolphins have only two obvious limbs (their flippers), as em- bryos they have two hind-limb buds, for a total of four limbs.
Lanc
elet
(o
utgr
oup)
Lam
prey
Tuna
Sala
man
der
Turt
le
Leop
ard
Dol
phin
0
0
0
0
0
0 1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
0
0
0
0
0
0
0
0
0
0
0
0
0 0
1
1
1*
1
1
1
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Figure 26.UN07