Title: Evolution of Development
1- Evolution of Development
- Chapter 25
2Evolutionary Paradox
- Phenotypic diversity
- Different genes
- Similar genes deployed and regulated differently
- Direct and indirect development
- Sea urchins
- Changes in patterns of developmental gene
expression - Genes have not changed, patterns of expression
have
3Evolutionary Paradox
- Direct and indirect sea urchin development
4Evolutionary Paradox (Cont.)
- Direct and indirect sea urchin development
5Evolutionary Paradox
- 2 dozen gene families regulate animal and plant
development - Hox genes establish the body plan by specifying
when and where genes are expressed - Hox genes code for proteins that bind to
regulatory region of other genes - Plants shoot growth and leaf development
- Animals establish body plans
6Evolutionary Paradox
- MADS box genes code for a DNA-binding motif
- Establish the body plan of plants (flowers)
- Highly conserved
- Understanding how development evolved requires
understanding - Genes, gene expression, development, and
evolution - Alteration of the timing or position of gene
expression
7Evolutionary Paradox
- Heterochrony alterations in timing of
developmental events due to a genetic change - Mutation in a gene small plant that flowers
quickly - Most mutations that affect developmental
regulatory genes are lethal - If mutation leads to increased fitness new
phenotype will persist
8Evolutionary Paradox
- Homeosis alterations in the spatial pattern of
gene expression - Bithorax fruit fly homeotic mutation which
produces two pairs of wings - Antennapedia fruit fly leg where an antenna
should be - Mutations can arise spontaneously or by
mutagenesis in the laboratory
9- Mutations in Fruit Fly Wings
Normal fruit fly with one set of wings
Mutant fruit fly with two sets of wings
10Evolutionary Paradox
- Coding sequence of a gene can contain multiple
regions with different functions - Regulatory region change may alter time or place
of gene expression - Changes in signaling pathways
- Coordinating information about next cell
- Information about external environment
- Receptor in a different cell type
- Alter targets
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13Gene Mutation
- Brassica oleracea ancestral species
- Cauliflower and broccoli stop codon
- CAL and Apetala1 gene changes regular flowers
into masses of arrested flower buds - CAL was cloned from Brassica a stop codon, TAG,
was found in the middle of the sequences when
analyzed
14Gene Mutation
- Evolution of cauliflower and broccoli
15Gene Mutation
- Cichlid fish jaws demonstrate morphological
diversity - Different species acquire different niches based
on feeding habits - Rammers long snouts
- Biters intermediate snout
- Bottom feeders short snouts
- Two genes shape and size
16Gene Mutation
17Gene Mutation (Cont.)
18Same Gene New Function
- Ancestral genes co-opted for new functions
- Evolution of chordates
- Brachyury gene of ascidians (notochord, no
vertebrate) encodes a transcription factor - Expressed in developing notochord
- Brachyury gene, homologue in mollusk is
associated with anterior-posterior axis
specification
19Same Gene New Function
- Protein domain T box, transcription factor.
- Turns on or off a gene or genes
20Same Gene New Function
- Mutation in Brachyury in dogs
- Cause short tail to develop
- Humans have wild-type of the gene
- Limb formation bird wing human forearm
- Tbx5 transcription factor gene family with T
box domain - Tbx5 encodes a protein that turns on a gene or
genes to make a limb
21Same Gene New Function
- Mutations in human Tbx5 cause Holt-Oram syndrome
forelimb and heart abnormalities - Tbx5
- Gets limb development started
- Regulates the expression of other genes
- 4-D development 3-D space and time
- Tbx5 proteins bind to different genes in birds
and in humans
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23Different Genes, Convergent Function
- Homoplastic (analogous) structures
- Same or similar functions
- Arose independently
- Phylogenies reveal convergent events
- Origin of convergence difficult to understand
- Different developmental pathways may have been
modified
24Different Genes, Convergent Function
- Insect wing patterns demonstrate homoplastic
convergence - Origins of patterns recruitment of existing
regulatory programs for new functions - Sensory bristles and scale development initiated
by achaete-scute transcription factor
25- Development of scales structures inverted from
bristles - Daughter cell neuronal connection dies
- Pigment production triggered
26Different Genes, Convergent Function
- Flower shapes have also altered in a convergent
way - Radially symmetrical flower two identical parts
when cut across center -daisies, roses, tulips
27Different Genes, Convergent Function
- Bilaterally symmetrical flowers mirror-image
halves on each side of a single central axis
peas, snapdragons - Bilaterally symmetrical flowers attractive to
their pollinators - Shape may be reason for evolutionary success
orchid
28Different Genes, Convergent Function
- Cycloidia (CYC) gene responsible for bilateral
symmetry of snapdragon - Snapdragons with mutations in CYC have radially
symmetrical flowers - Radial symmetry is the ancestral condition
- Some radially symmetrical flowers have
bilaterally symmetrical ancestor - Loss of CYC function radial symmetry
29Different Genes, Convergent Function
- Gain of bilateral symmetry arose independently
among some species because of CYC gene - Convergent evolution through mutations of the
same gene - Other genes also play a role in convergent
evolution of bilateral symmetry
30Different Genes, Convergent Function
With gene expressed
Without gene expressed
31Duplication and Divergence
- Gene duplications of paleoAP3 led to
flowering-plant morphology - MADS box gene duplicated
- Gave rise to PI and paleoAP3 genes
- Ancestor genes affected stamen development
(function retained) - paleoAP3 duplicated to produce AP3
- AP3 duplicated again gained a role in petal
development
32Duplication and Divergence
- Petal evolution through gene duplication
33Duplication and Divergence
- Gene divergence of AP3 altered function to
control petal development - Mutant ap3 plants do not produce either petals or
stamens - PI and AP3 proteins can bind to each other
- regulate transcription of genes needed for stamen
and petal formation
34Duplication and Divergence
- AP3 has acquired a domain necessary for petal
development
35Functional Analysis
- Functional analysis range of experiments
designed to test the function of a gene in
different species - Sequence comparison essential
- Need to distinguish paralogues from orthologues
- Single base mutation can change active gene into
an inactive pseudogene - Functional genomics experimenting to demonstrate
actual function of the gene
36Case Study
- Diversity of eyes in the natural world
- Morphological evidence indicates eyes evolved at
least twenty times - Convergent evolution Homoplastic
37Fly and Mouse eye
- Most recent ancestor no sight
- Pax6 initiates eye development
- Triggers lens formation in insects and
vertebrates - Walter Gehring inserted mouse Pax6 into genome
of a fruit fly - Created transgenic fly
- Pax6 gene turned on by regulatory factors in the
flys leg
38Fly and Mouse eye
- Mouse Pax6 makes an eye on the leg of a fly
39Case Study
- Pax6 and eyeless cave fish. Pax6 gene expression
reduced. Eyes start to develop, then degenerate
40Case Study
- Pax6 expression correlates with ribbon worm
eyespot regeneration
41Case Study
- Pax6 is not required for planaria eyespot
regeneration
42- Hypothesis 1 Pax6 gene and its homologues
- Eye development may have a single evolutionary
line - Hypothesis 2 Pax6 gene could have had a
regulatory role in the forehead of early animals - Eye development may have occurred over and over
and Pax6 has been independently co-opted over and
over for eye development