01history Slides

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    History of Developmental Biology

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    Embryology vs. Developmental Biology

    Developmental Biology: Includes the

    study of post-embryonic changessuch as growth/maturation,

    metamorphosis, regeneration, aging.

    Embryology: Descriptive study of

    embryonic development includes allmulticellular organisms (plants,

    animals, fungi).

    Developmental Biologyis descriptive but also

    incisive: what are the

    mechanisms?

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    5th century BC :

    Aristotle favored epigenesis

    17th century:

    Marcello MalpighiChick embryology description(s) should

    have confirmed Aristotles ideas

    Preformation regained popularity

    History: Epigenesis vs. Preformation

    Preformation: Everything in the embryo is pre-formed and simply

    grows during development.

    Epigenesis: New structures arise progressively during development.

    A preformed embryo(homunculus) within

    sperm (1694)

    Malpighis drawings ofchick embryos (1673)

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    19th century:More descriptive embryology

    Evolution: ontogeny recapitulates phylogeny

    Cell Theory

    Genetics + Development

    Germ cells vs. somatic cells (Weissmann)

    History: Cell Biology and Genetics

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    Genes Proteins Cell Activities Developmental Processes

    History: Cell Biology and Genetics

    19th century:More descriptive embryology

    Evolution: ontogeny recapitulates phylogeny

    Cell Theory

    Genetics + Development

    Germ cells vs. somatic cells (Weissmann)

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    19th century:More descriptive embryology

    Evolution: ontogeny recapitulates phylogeny

    Cell Theory

    Genetics + Development

    Germ cells vs. somatic cells (Weissmann)

    History: Cell Biology and Genetics

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    History: Nuclear Determination vs. Regulation

    The mosaic model (Weismann): nuclear determinants are asymmetrically

    distributed in zygote these determine fate of embryonic cells.

    The regulation hypothesis suggests that embryonic development can adjust

    to the loss of cells.

    Rouxs experiment (1880s) on

    frog embryos supported the

    mosaic model

    Drieschs experiment (1880s) on

    sea urchin embryos supported

    the regulation hypothesis

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    20th century:

    Johannsen genotype = phenotype(gene X environment interaction)

    Mangold and Spemann - Induction: One cell (or tissue)influences the development of another cell (or tissue).

    History: Genotype vs. Phenotype, Induction

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    Throughout history, and today :

    Model organisms

    Mouse, chick,Xenopus, zebrafish,Drosophila, c. elegans, arabidopsis

    Model Organisms

    MOUSE (Mus musculus)

    Advantages: Genetic manipulation, history of use, mammal, fast generation time.

    Disadvantages:In utero development, costly.

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    Throughout history, and today :

    Model organisms

    Mouse, chick,Xenopus, zebrafish, drosophila, c. elegans, arabidopsis

    Model Organisms

    CHICK (Gallus domesticus)

    Advantages:In ovo development, history of use, amniote.

    Disadvantages: Genetic manipulation not (yet?) possible; large ns difficult.

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    Throughout history, and today :

    Model organisms

    Mouse, chick,Xenopus, zebrafish, drosophila, c. elegans, arabidopsis

    Model Organisms

    AFRICAN CLAWED FROG

    (Xenopus laevis and Xenopus tropicalis)

    Advantages:In ovo (rapid) development, large embryos, history of use, inexpensive.

    Disadvantages:X. laevis is tetraploid.

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    Throughout history, and today :

    Model organisms

    Mouse, chick,Xenopus, zebrafish, drosophila, c. elegans, arabidopsis

    Model Organisms

    ZEBRAFISH (Danio rerio)

    Advantages:In ovo (rapid) development, genetic manipulation, history of use, inexpensive.

    Disadvantages: ???? (o.k., so Im biased)

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    Throughout history, and today :

    Model organisms

    Mouse, chick,Xenopus, zebrafish, drosophila, c. elegans, arabidopsis

    Model Organisms

    FRUIT FLY (Drosophila melanogaster)

    Advantages:In ovo (rapid) development, genetic manipulation, history of use, inexpensive.

    Disadvantages: Invertebrate

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    Throughout history, and today :

    Model organisms

    Mouse, chick,Xenopus, zebrafish, drosophila, c. elegans, arabidopsis

    Model Organisms

    ROUNDWORM (caenorhabditis elegans)

    Advantages:In ovo development, genetic manipulation, history of use, inexpensive.

    Disadvantages: Invertebrate

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    Throughout history, and today :

    Model organisms

    Mouse, chick,Xenopus, zebrafish, drosophila, c. elegans, arabidopsis

    Model Organisms

    MOUSE-EAR CRESS (arabidopsis thaliana)

    Advantages: Rapid generation time, genetic manipulation, history of use, inexpensive.

    Disadvantages: As a plant model, not many.

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    Modern Developmental Biology

    Developmental genetics

    Diseases and disorders of development/teratology

    Tissue repair and replacement/stem cells

    Aging and cancer

    Agriculture and food science

    Evolutionary biology

    Applications

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    An introduction to the Developmental Biology literature

    Journals (original research articles = primary literature):

    Developmental BiologyDevelopmental Dynamics

    Developmental NeurobiologyBMCDevelopmental Biology

    Development,Genes and Evolution

    Differentiation

    Genes and DevelopmentInternational Journal of Developmental Biology

    Development

    DevelopmentalCell

    Mechanisms of Development

    Science

    NatureProceedings of the National Academy of Science

    Cell

    Neuron

    Search via PubMed: http://www.ncbi.nlm.nih.gov/sites/entrez

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    Most research articles involve the use of model organisms to probe the function of

    genes/proteins for a specific developmental process.

    Retinal Homeobox 1 is Required for Retinal Neurogenesis

    and Photoreceptor Differentiation inEmbryonic Zebrafish

    Most make use of gain-of-function (GOF) or loss-of-function (LOF) approaches, using

    genetic, molecular, or pharmacological tools to manipulate the target gene/protein.

    LOF approach = antisense (morpholino) oligonucleotides targetingrx1 and rx2

    Others will utilize cell/tissue transplantation techniques to probe developmental

    potential of those cells/tissues

    An introduction to the Developmental Biology literature

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    Most of the data are collected as images showing histology of the developing structure

    of interest, and/or gene expression (in situ hybridization to localize mRNA, orimmunocytochemistry to localize corresponding protein) within that structure.

    There is a LOTof jargon.

    An introduction to the Developmental Biology literature