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Lecture Notes - Lecture 1, Developmental Biology, BioD104, UC Irvine

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Typed class notes covering lecture 1 in the Development Biology course (code BioD104) at UCI. Document comes with color-coded notes and textbook diagrams.

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Publié le
8 août 2024
Nombre de pages
4
Écrit en
2019/2020
Type
Notes de cours
Professeur(s)
Dr. ken cho
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Lecture 1 Abbreviation Key:
Friday, August 2, 2019 10:37 PM
b/c = because
b/w = between
w/ = with
expt = experiment
• Epigenesis: organisms develop via a sequence of steps where cells differentiate and organs form, during
ex. = example
different stages. New structures arising progressively -> need to acknowledge temporal and spatial
arrangement/location.
• Determinant development/Mosaic Theory: argues that 1-cell zygote contains specific determinants that
are distributed unequally b/w daughter cells (asymmetric cell division). Wilhelm Roux experiment
○ Determinants are spatially located.
○ Roux expt: stated separate function of cells had already been determined b/c specific determinants
went into certain cells during cell division-> Mosaic model.
• Regulative development: an embryo can regulate aspects of development even when some cells are lost.
Hans Driesch experiment
○ Mosaic Theory cannot explain Driesch's expt where separated cells still form the same (yet smaller) Environment encourages
organism that also arose from controlled 2-cell stage. specified cell to take on
○ If the Mosaic Theory was true, inducing apoptosis to one of the cells during the 2-cell stage would another cell fate. Determination Specification
effect the development of the organism, b/c a portion of determinants would be lost. But it didn't…
○ Driesch's work refuted both preformation and Mosaic Theory. Cell-to-cell interactions are important.
• NOW WE KNOW Development is all about regulation of gene expression.
○ Genome is normally identical in every cell, yet cells in an embryo differ b/c they express different
genes.
○ Gene expression is controlled by upstream developmental genes.
○ How is gene expression regulated? With enhancers? Enhancers interact w/ the promoter, which
allow them to control gene expression.




▪ Promoter: located before the coding gene -> give you where the gene is expressed in DNA.
▪ Enhancers: are at multiple locations upstream promoter. Can hold information on associated
genetic disease. -> Interest of study
• Development is progressive:
○ Early embryonic cells have great developmental potential.
○ The ability to switch fates (pluripotency) decreases as development progresses.
○ Start expressing only necessary genes; genes become "narrower and narrower" in their cell
lineage/fate.
○ Cells go thru a series of steps before acquiring their final differentiated states…
• Specification: the ability to differentiate autonomously when placed in a neutral environment (petri dish,
test tube, saline solution). Cell fate depends on environment. Reversible.
• Determination: the ability to differentiate autonomously even when placed into another region of the
embryo. Aka the cell differentiates according to it's original fate. Irreversible.
• Differentiation: process where one cell type changes to another, allowing morphological
changes/displaying specific phenotypes.
• How can cells acquire different characteristics? What mechanism determines different lineages?
1. Mosaic strategy: cytoplasmic localization + asymmetric cell division = distinct daughter cells
a. The properties of these cells will be defined by their lineage, not by their environmental cues.
b. One cell would acquire determinants, the other would not. -> Different cell fates
2. Via induction
a. Induction: occurs when a cell signal influences development of other cells.
b. Competency: the ability to respond to inductive signals. Competent cells respond to signals.
c. The response can be stage-specific (temporally regulated). How? Commitment/being competent
is a stage itself that can be controlled in development.
d. New structures are induced by cell signaling. Ex. Formation of eye cups.
• Inductive interactions can be:
○ Permissive: A cell makes only one kind of response to an inducing signal, and makes it when a
given level of signal is reached: a single outcome, all or none. All info is present in responder cells.
Responder cells hold the control. One response.
○ Instructive: different concentrations elicit different responses/cell types (dose-dependent effects).
Inducing cells provide info to responder cells. Inducing cells hold control. Concentration of
inducing cells -> various possible responses.
• Multiple cell types can be generated by a morphogen.
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NotesByAlixD

I have a Biological Sciences degree from UC Irvine class of 2021. Most of my documents will be from courses I've taken during my time at UCI. No answers to exams or quizzes, just study guides and lecture notes.

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