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KS_JRC_MOLEVO
Molecular Evolution Krishnendu Sinha
Assistant Professor
Department of Zoology
Jhargram Raj College
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= Lamarkism
= Darwinism
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Darwinism Neo-Darwinism
Natural selection (Positive & Negetive) Natural Selection
Sexual Selection
(Runaway Hypothesis. Handicap Principle etc.)
Genetic drift (Bottleneck, Founder Effect etc.)
Gradualism Saltation
Neutral Selection
Individualism Population and gene pool
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MOLECULAR PHYLOGENY
1. Basic concepts of phylogeny
2. Construction of Phylogenetic Trees
a. Phylogenetic Inference-distance Methods, Parsimony Methods,
Maximum Likelihood Method
b. Amino Acid Sequences and Phylogeny
c. Nucleic Acid Phylogeny
3. Nucleotide Sequence Comparisons and Homologies
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Phylogeny is the history of the evolution of a species or group,
especially in reference to lines of descent and relationships among broad groups of organisms
…the evolutionary history of a group of taxa
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Character Any physical structure (macroscopic, microscopic or molecular)
or behavioural system that can have more than one form (character state q.
v.), the variation in which potentially provides phylogenetic information.
Character state Any of the possible. distinct conditions that a character
can display. Sometimes also loosely termed character
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Cladistics In general the process of defining evolutionary relationships between taxa
using evidence from extant taxa. Originally formulized by Hennig, now comprising a
number of variously related methodologies (Fitch, 1984).
Cladogram A dendrogram (tree diagram) specifically depicting a phylogenetic
hypothesis and therefore based on synapomorphies. A cladogram generally only
indicates the branching pattern of the evolutionary history, cf. phylogram (Mayr.
1965).
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Usually same in function
Usually different in function
Homologs
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Evolutionary History of an Allopolyploid. An ancestral
genome undergoes a speciation event, resulting in two
diploid species. The genes, which descended from a
common gene in the ancestor, are orthologs. Evolution
occurs after speciation, including structural
rearrangements, gene duplications, and gene
movement. On polyploidization, genes that were once
orthologs are now homoeologs. Homoeologous
relationships can be one-to-one, one-to-many, or many-
to-many depending on the number of duplications
since speciation of the progenitors.
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Five Stages of Phylogenetic Analysis
Molecular phylogenetic analyses can be divided into five stages:
(1)selection of sequences for analysis
(2)multiple sequence alignment of homologous protein or nucleic acid sequences
(3)specification of a statistical model of nucleotide or amino acid evolution
(4)tree building
(5)tree evaluation
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Tree Topology
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Internal node
(‘hypothetical ancestor’)
Root
Branch
Terminal node (‘Leaf’)
Internal node
(‘hypothetical ancestor’)
Branch
Terminal node (‘Leaf’)
Polytomy
Fully Resolved
Partially Resolved
ABCDE
ABCD E
A B C D E
Tree representation
Tree terminology
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Maximum Parsimony
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Taxon
Nucleotide positions
1 2 3
A G G G
B G T G
C T G T
D T T T
Phylogenetic reconstruction
A
G..
B
G..
C
T..
D
T..
G..
T..
T..
A
..G
B
..G
C
..T
D
..T
..G
..T
..T
A
.G.
B
.T.
C
.G.
D
.T.
.T.
.T.
.T.
D
T..
A
G..
B
G..
C
T..
T..
T..
T..
A
..G
B
..G
C
..T
D
..T
..T
..T
..T
A
.G.
B
.T.
C
.G.
D
.T.
.G.
.T.
.T.
A
GGG
C
GTG
B
TGT
D
TTT
GTG
TTT
TTT
A
GGG
B
GTG
C
TGT
D
TTT
GTG
TTT
TTT
Total length = 4
Total length = 5
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A
C
C
A
G
[A,C]
[A,G]
[C,A,G]
[A,C]
Length = 1+1+1+0 = 3
AC
C
A
G
[A]
[A]
[A]
[A]
AC
C
A
G
[C]
[C]
[A]
[C]
Length= 3
Length= 3
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Tree Space Searching
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Consensus Tree
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A B C D E F COUNT
* - * -- -
A F B
E D
C
A
F
B
E D C
A C B
E F
D
A
C
E
B
F
D
- - - -* *
* * - -- -
- * - -* -
- - - *- *
* - * *- -
- * * -- -
* * * -- -
A D
E B
F
C A D
E B
F
C
I
III
III
III
II
I
I
I
A B C D E F COUNT FREQUENCY
* - - - * - III 60
* - * - * - III 60
- * - * - - I 20
* - * - - - I 20
- - - * - * III 60
* - - - * * I 20
- * * - - - II 40
- - * - * - I 20
KS_JRC_MOLEVO
A B C D E F COUNT FREQUENCY
* - - - * - III 60
* - * - * - III 60
- * - * - - I 20
* - * - - - I 20
- - - * - * III 60
* - - - * * I 20
- * * - - - II 40
- - * - * - I 20
A B C D E F COUNT FREQUENCY
* - - - * - III 60
* - * - * - III 60
- - - * - * III 60
- * * - - - II 40
- * - * - - I 20
* - * - - - I 20
* - - - * * I 20
- - * - * - I 20
CA
E
D
FB
CCA
E
D
F
C
B
Majority Rule Consensus Tree Construction
A
E
D
FC
B
60 60 60
Consensus Tree
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Distance Matrix Based Methods
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D12~d12= a+b+c
Goal:
D13~d13= a+d
D14~d14= a+b+e
D23~d23= d+b+c
D24~d24= c+e
D34~d34= d+b+e
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KS_JRC_MOLEVOf(x) = ax2 + b x + c (where a, b, and c are real numbers and a ≠ 0)
δf(x)/δa = 0
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Model Based Correction for Superimposed Substitutions
Goal: try to infer the real number of evolutionary events (the real distance based on
a) Observed data (sequence comparison)
b) A model on how evolution has occurred
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Clustering Algorithm: Neighbor Joining (NJ)
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D C
X
10 4
53
53
53
53
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A B
Y
13 4
D C
X
10 4
-42
-42
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A B
Y
13 4
D C
X
10 4
4
A
Y
13
4
C
D
X
4
10
4
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Models of Evolotion
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Maximum Likelihood
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A
C
T G
T
A
t1
t2
t3
t4
t5
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Ancestral Reconstruction
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References
KS_JRC_MOLEVO
Lecture series of Dr. Anders Gorm Pedersen, Head of Section & Professor, Department of Health Technology, Technical
University of Denmark, Kemitorvet on Molecular Evolution at Coursera
&
KS_JRC_MOLEVO

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Molecular evolution