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This set of flashcards is designed to help students review key concepts and vocabulary related to embryology and developmental biology as outlined in their lecture notes.
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Embryo
Name for organisms between fertilization and birth.
Model Organism
A species that multiple scientists agree to study, share information on, and develop tools for, in order to accelerate scientific progress.
Homologous Structures
Structures in different species that share a common evolutionary origin, such as mammalian forelimbs and bat wings, which both have five digits.
Limb Bud
An embryonic structure formed by proliferating mesenchymal cells covered by ectoderm that gives rise to limbs.
Cell Behaviors Used During Development
Processes including cell growth, cell differentiation, cell morphogenesis, movement, adhesion, and division that shape the developing organism.
Cell Differentiation
The process by which unspecialized cells become specialized cells with distinct structures and functions, occurring in stages from a stem cell to a progenitor cell and finally a terminally differentiated cell.
Cell Morphogenesis
The biological process governing how cells generate, change, and organize their shape and structure, transforming single cells into complex, functional tissues and organisms through genetic programs and mechanical forces.
Cell Growth
An increase in the total mass and volume of a cell when biosynthesis exceeds degradation, coordinated with the cell cycle to ensure proper cell size and tissue growth.
Genome Equivalence
The principle that all cells arise from a single cell and contain the same genome, despite differences in cell type.
Experimental Test of Genome Equivalence
Replacing an egg’s nucleus with the nucleus from a differentiated (post-development) cell to determine whether the DNA retains full developmental potential.
Differential Gene Expression
The process by which cells become different from one another based on the unique combination of genes that are active or expressed, producing different proteins.
Evidence for Differential Gene Expression
RNA sequencing results showing different expression patterns of genes in different cell types.
Ectopic Organ Development
The formation or presence of tissues or organs in abnormal anatomical locations due to disordered embryogenesis.
Cause of Ectopic Organ Development
Mis-expression of genes.
Chromatin
The DNA–protein complex in eukaryotic cells that regulates access to genes for transcription.
Cis-Regulatory Elements
Non-coding DNA sequences (promoters, enhancers, silencers) that regulate when and where nearby genes are expressed.
Transcription Factors (Regulators)
Proteins that bind DNA with precise sequence recognition to regulate gene expression.
Coactivators
Proteins that act as transcriptional regulators and help activate transcription without directly binding DNA.
Enhancers
Cis-regulatory DNA elements that determine when, where, and how much a gene is expressed, enabling cell-type-specific expression.
Enhancer Modularity
The property that individual enhancers independently control specific aspects of gene expression.
Reporter Genes
Molecular tools used to track gene expression by producing detectable signals such as fluorescence or luminescence.
Trans-Regulatory Factors
Diffusible gene-encoded molecules, primarily proteins, that regulate the expression of target genes located elsewhere in the genome.
Cis vs. Trans Regulation
Cis acts from the same DNA molecule to regulate nearby genes, while trans acts from a different molecule to regulate gene expression.
Cis-Regulatory Mutations
Mutations in regulatory DNA that can lead to congenital malformations such as aniridia, Pierre Robin sequence, and triphalangeal thumb.
Experimental Embryology
The study of development by observing and physically manipulating embryos before genetics and molecular biology.
Cleavage Stage
The initial phase of embryonic development characterized by rapid mitotic divisions without overall growth.
Blastula
A hollow, spherical embryonic stage formed after cleavage, consisting of a layer of cells surrounding a fluid-filled cavity called the blastocoel.
Gastrulation
An early developmental process where a blastula reorganizes into a multilayered structure called the gastrula.
Spemann–Mangold Organizer Experiment
A landmark experiment demonstrating embryonic induction where specific cells direct the development of others.
Organizer
A specialized region of embryonic tissue that directs the developmental fate of surrounding cells and patterns the body axes.
Fertilization
The event that breaks radial symmetry in the egg and initiates embryonic development.
Anterior (Ventral)
The front side or surface of the body.
Posterior (Dorsal)
Terms referring to the back side of the body, where dorsal is often used for the back of the hands/feet.
Animal Pole
The upper, metabolically active hemisphere of an egg or embryo associated with anterior (head) structures.
Vegetal Pole
The bottom region of an egg or embryo characterized by high yolk concentration, typically associated with posterior (tail) structures.
Sperm Entry
Introduces centrioles and proteins that nucleate microtubules and stimulate cortical rotation.
Gray Crescent
The dorsal region of the embryo formed after cortical rotation that will give rise to the organizer.
Cortical Rotation
A critical process in frog eggs that breaks radial symmetry to establish the dorsal-ventral axis.
Wnt/β-Catenin Signaling
A pathway wherein Wnt signaling stabilizes β-catenin, allowing it to activate specific gene transcription and play a role in establishing the dorsal-ventral axis.
Ectoderm
The outermost primary germ layer in an embryo responsible for developing the nervous system and skin.
Mesoderm
The middle primary germ layer that forms muscles, connective tissues, and the circulatory system.
Endoderm
The innermost primary germ layer that functions as foundational tissue for the digestive and respiratory tracts.
Autonomous Specification
Cell fate determination driven by internal cues that are independent of external signals.
Conditional Specification
Cell fate determination dependent on signals from neighboring cells.
Induction
A developmental concept where one group of cells influences the behavior of adjacent cells.
Mesoderm-Inducing Signals
Secreted signals from the vegetal pole that induce mesoderm formation.
Fate Mapping
Marking a cell and following it through development to determine its eventual fate.
Lineage Tracing
Tracking which cells arise from a specific progenitor cell over time.
Thomas Hunt Morgan
Demonstrated that genes are located on chromosomes using Drosophila, establishing the chromosome theory of inheritance.
NĂĽsslein-Volhard and Wieschaus
Identified genes controlling embryonic patterning in Drosophila through large-scale mutagenesis screens.
Mutagenesis Screen
A method of inducing random mutations and screening for developmental phenotypes.
Maternal Genes
Genes whose products are deposited in the egg and control early development before zygotic transcription.
Zygotic Genes
Genes transcribed after the mid-blastula transition, controlling later developmental processes.
Complementation Groups
Groups of mutations that, when crossed, can indicate if the mutation is in the same gene.
Bicoid
A transcription factor that directs the specification of anterior structures in a concentration-dependent manner.
Morphogen
A molecule that forms a gradient and induces different cell fates at different concentrations.
Even-Skipped (eve) Enhancers
Specific promoter regions of the eve gene that control distinct transcriptional stripes in the embryo.
To confirm genome equivalenceÂ
Take a nucleus from an old cell with its (post-development) DNA and use it to replace anegg’s (pre development) DNA. It will tell you if the DNA is the same and has equivalence. Main Question: Does it support development?
Yes: development does not change DNA
No: Development does change DNA
What can cause ectopic organ development?Â
Mis-expressing genes
Eukaryotic DNA exists as a DNA/protein
complex called
Chromatin
Wnt signaling results in b-catenin induced transcription
Wnt pathway
components like
Dishevelled (Dsh) and
GBP move toward the
future dorsal side. This
movement aligns with
microtubules, leading to
dorsal accumulation of đť›˝-
catenin and inducing the
Spemann organizer. This
localized accumulation
leads to the stabilization
and nuclear localization
of đť›˝-catenin, triggering
dorsal-specific gene
expression (e.g., siamois)
and subsequent dorsal
axis formation.
Significance: This
process ensures the
precise, localized
activation of the Wnt/đť›˝-
catenin pathway
necessary for
establishing the dorsal-
ventral axis in amphibian
embryos.
Why is gastrulation triggered?
Mesoderm differentiation during germ layer specification generates cells expressing a migratory program
Which types of proteins could cells use to talk to each other during induction?
Secreted proteins
Cell surface ligands that bind cell surface receptors
Extracellular matrix proteins that bind cell surface receptors
Fate mapping versus cell lineage tracing
Goal: Fate
mapping
identifies where
cells go and what
they become.
Lineage tracing
determines which
cells arose from a
specific
progenitor.
Perspective:
Fate maps are
often prospective
(projecting future
fate). Lineage
tracing is often
retrospective
(reconstructing
history).
Genome Equivalence - What would violate it?
Loss of genes in differentiated cells; different gene expression does NOT violate genome equivalence
Enhancer–Promoter Interaction
Enhancers activate transcription through DNA looping that brings enhancer-bound proteins into contact with promoters.
Cortical Rotation — What if microtubules are disrupted?
Wnt pathway components cannot localize dorsally, the gray crescent does not form, and dorsal–ventral axis fails.
Mesoderm Specification Type
Mesoderm is conditionally specified and requires inductive signals from neighboring cells.
Maternal-Effect Genes — When do they act?
Before the mid-blastula transition, using mRNA and proteins deposited by the mother.
Complementation Test — Failure to Complement Means
The mutations affect the same gene.
Reporter Genes in Fate Mapping
Reporter genes can be used for fate mapping if the label is inherited by descendant cells.
Apical Ectodermal Ridge (AER)
Ectodermal structure that promotes limb outgrowth along the proximal–distal axis by maintaining mesenchymal proliferation
Effect of Removing AER
Distal limb truncation; proximal structures still form; limb identity remains unchanged.
Zone of Polarizing Activity (ZPA)
A mesenchymal signaling center that patterns the anterior–posterior axis of the limb using Sonic hedgehog signaling.
Effect of Removing ZPA
Loss of proper anterior–posterior digit identity.
Effect of Ectopic ZPA
Mirror-image duplication of digits.
Sonic Hedgehog (Shh) in Limb Development
A morphogen secreted by the ZPA that specifies digit identity in a concentration-dependent manner.
Human Limb Defects Linked to Shh Misregulation
Polydactyly, digit malformations, mirror-image duplications.
Limb Identity Is Determined By
Mesoderm, not ectoderm