CHAPTER 25 LECTURE SLIDES Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Evolution of Development Chapter 25 2 • To explain differences in species, we need to look at changes in genes that have their effect by altering development and thus phenotype • Phenotypic diversity has resulted not from large changes in genes but from changing patterns of expression 3 • 2 closely related sea urchin species have very different developmental patterns • 2 forms have very similar genes • Dramatic changes in gene expression during development • Adult forms nearly the same in both 4 • About 2 dozen gene families regulate animal and plant development • Hox (homeobox) 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 5 • MADS box genes code for a DNAbinding motif – Establish the body plan of plants, especially flowers – MADS box highly conserved but variation in other coding region sequences • Transcription factors and genes coordinate development – Changes can have dramatic effects on the development of an organism 6 Heterochrony • Alterations in timing of developmental events due to a genetic change – Could affect a gene that controls transition of plant from juvenile to adult – Mutation results in small plant that flowers quickly • Most mutations that affect developmental regulatory genes are lethal • If mutation leads to increased fitness, then new phenotype will persist 7 Homeosis • Alterations in the spatial pattern of gene expression • 4-winged Drosophila requires mutation in 3 genes in Bithorax complex • Drosophila Antennapedia has a leg where an antenna should be • Mutations can arise spontaneously or by mutagenesis in the laboratory but bizarre phenotypes would have little survival value in the wild 8 • Coding sequence of a gene can contain multiple regions with different functions • Regulatory region change may alter time or place of gene expression – Hetrochrony or homeosis – Downstream targets the same but cells that express target genes or timing of expression could change 9 10 11 Gene Mutations • Brassica oleracea subspecies have very diverse phenotypes – Wild cabbage, kale, tree kale, red cabbage, green cabbage, brussels sprouts, broccoli, and cauliflower • CAL and Apetala1 gene mutation changes regular flowers into masses of arrested flower buds 12 • CAL was cloned from Brassica – Stop codon, TAG, was found in the middle of the sequences for broccoli and cauliflower – Stop codon appeared after ancestors of broccoli and cauliflower diverged but before broccoli and 13 cauliflower diverged from each other • Cichlid fish jaws demonstrate morphological diversity – Cichlid fish in Lake Malawi in East Africa – In less than a few million years, hundreds of species evolved from a common ancestor – Different species acquired different niches based on feeding habits • Rammers: long snouts • Biters: intermediate snout • Bottom feeders: short snouts 14 15 • 2 genes, of yet unknown function, are likely responsible for the shape and size of the jaw • Regulating the length versus the height of the jaw may well be an early and important developmental event • Range of jaw forms appears to have persisted because the cichlids establish unique niches for feeding within the lake 16 Same gene, new function • Evolution of chordates can partially be explained by the co-option of an existing gene for a new function – Ascidians have a notochord but no vertebrate • Brachyury gene encodes a transcription factor expressed in developing notochord • Homologues found in invertebrates 17 – Region of Brachyury gene encodes protein domain called T box, transcription factor • Transcription factor turns on or off a gene or genes • In mice and dogs, Brachyury mutation causes a short tail • Humans have wild-type Brachyury so other genes must be needed for a tail 18 • Limb formation – Most tetrapods have 4 limbs – 2 forelimbs and 2 hindlimbs – Bird wings and human forearms are homologous structures – Humans and birds both express Tbx5 gene in developing limb buds – What seems to have changed as birds and humans evolved are the genes that are transcribed because of the Tbx5 19 protein • In the ancestral tetrapod, perhaps Tbx5 protein bound to only one gene and triggered transcription • In humans and birds, genes are expressed in response to Tbx5 protein, but they are different genes 20 Different 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 – In other cases not clear whether it is the same or different genes responsible 21 • Insect wing patterns – Can protect them from predation or allow them to thermoregulate – Origins of patterns best explained as recruitment of existing regulatory programs for new functions – Sensory bristles and scale development initiated by achaete-scute transcription factor 22 • Scales derived from bristles – Structure inverted – Daughter cell neuronal connection dies – Pigment production triggered 23 • Flower shapes have also altered in a convergent way – Radially symmetrical flower: two identical parts when cut across center • Daisies, roses, tulips – Bilaterally symmetrical flowers have mirrorimage halves • Snapdragons, mints, peas • Shape may be important in their evolutionary success 24 • Cycloidia (CYC) gene responsible for bilateral symmetry of snapdragon – Snapdragons with mutations in CYC have radially symmetrical flowers • Radial symmetry is the ancestral condition • Gain of bilateral symmetry arose independently among some species because of the CYC gene – Convergent evolution through mutations of the same gene • In other cases, CYC is not clearly responsible 25 for the bilateral symmetry Gene duplication and divergence • Gene duplications of paleoAP3 led to flowering-plant morphology – MADS box gene duplicated – Gave rise to PI and paleoAP3 genes – In ancestral plant, genes affected stamen development • This function has been retained – paleoAP3 duplicated to produce AP3 and an AP3 duplicate – AP3 gained a role in petal development 26 • Two gene duplications resulted in the AP3 gene in the eudicots that has acquired a role in petal development 27 • 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 • No petals will form if C-terminus motif of AP3 absent 28 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Petals Present Stamen Present YES YES AP3 Gene Construct Added to AP3 Mutant Arabidopsis Complete AP3 Gene MADS AP3 C terminus 29 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Petals Present Stamen Present YES YES NO NO AP3 Gene Construct Added to AP3 Mutant Arabidopsis Complete AP3 Gene MADS No AP3 C terminus MADS AP3 C terminus 30 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Petals Present Stamen Present YES YES NO NO NO SOME AP3 Gene Construct Added to AP3 Mutant Arabidopsis Complete AP3 Gene MADS No AP3 C terminus MADS PI C terminus replaces AP3 C terminus MADS AP3 C terminus PI C terminus 31 Functional Analysis • Range of experiments designed to test the actual 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 • Therefore, function can be inferred from sequence data but actual function has to be demonstrated experimentally • Functional genomics – experimenting to demonstrate actual function of the gene 32 Diversity of eyes case study • Explaining complicated structures was one of Darwin’s greatest challenges • Incremental improvements in function could build a complex structure through natural selection 33 • Eyes of organisms are extremely different in many ways • Eyes are an example of convergent evolution – Homoplastic (analogous) structures rather than homologous • Morphological evidence indicates eyes evolved at least twenty times – Most recent common ancestor of all these forms had no ability to detect light 34 • Genes discovered that code for transcription factor important in lens development – Pax6 in mice, eyeless in flies • Sequence of genes highly similar – homologues • Walter Gehring inserted mouse Pax6 into genome of a fruit fly – Created transgenic fly – Pax6 gene turned on by regulatory factors in the fly’s leg – Eye formed on leg of fly 35 Mouse Pax6 makes an eye on the leg of a fly 36 • Transgenic fly results completely unexpected – Insects and vertebrates diverged more than 500 MYA – Large differences in eye structure – Expected eye development to be controlled by completely different genes 37 • Pax6 and eyeless cave fish • Pax6 gene expression reduced • Eyes start to develop, then degenerate 38 • Ribbon worms, Lineus sanguineus, also rely on Pax6 for eyespot development • Pax6 homologue has been cloned and has been shown to express at the sites where eyespots develop • In contrast, planarian worms do not rely on Pax6 for eyespot development 39 Eyespot Regenerated head Eyespot Regenerating head Probe for Pax6 Probe for Pax6 transcripts Pax6 expression correlates with ribbon worm eyespot regeneration 40 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. SCIENTIFIC THINKING Hypothesis: Pax6 is necessary for planaria eyespot regeneration which occurs when planaria are cut in half longitudinally. Prediction: Eyespot regeneration will not occur without Pax6 protein. Test: Cut Eyespot Eyespots Result: Eyespots regenerate. Conclusion: Pax6 is not required for eyespot regeneration in planaria. Further Experiments: Can you design an experiment to test if the planaria Pax6 gene can initiate eyespot development in a ribbon worm or eye development in a fly? Pax6 is not required for planaria eyespot 41 regeneration Several explanations for Pax6 • Eyes in different types of animals evolved truly independently, as originally believed – Possible Pax6 had role in forehead development and this role has been co-opted time and time again for eye development • Many think this unlikely since gene sequences and functional roles so similar – Suggests to many that Pax6 acquired its eye development role only a single time in the ancestor to all organisms using Pax6 for eye development 42