FATE MAP
FATE MAP
A fate map is a diagram or visual representation used in embryology to trace and predict the
developmental destiny of different parts of an embryo. It shows which regions of the early embryo (such
as the blastula or gastrula) will give rise to specific tissues, organs, and structures in the adult organism.
Fate mapping is essential for understanding cell differentiation, organogenesis, and morphogenesis.
Fate maps are invaluable in developmental biology, providing a visual representation of the embryonic
origins of adult tissues. They have evolved from simple observational studies to sophisticated techniques
involving genetic markers, significantly enhancing our understanding of developmental processes, disease
mechanisms, and evolutionary biology.
Embryonic regions with distinct fate are called Primordia or rudiments. Thus cells that will form
heart are called heart rudiments or heart primordia or prospective heart. Fate maps change over time,
because cells multiply and move relative to each other. A series of fate maps at consecutive stages show
the progression of different cells or regions through longer periods of developments.
History: The concept of fate mapping dates back to the late 19th and early 20th centuries. Notably, in
1905, Edwin Conklin produced detailed fate maps for ascidian embryos by observing natural pigmentation
patterns. Later, in 1929, Walter Vogt advanced the technique by using vital dye staining to trace cell
lineages in amphibian embryos.
Definition: A fate map indicates the future fate or developmental outcome of cells in an early embryo. It
helps embryologists understand how undifferentiated cells evolve into complex tissues and organs.
Stages Where Fate Mapping is Done:
1. Vital Dye Staining: Specific cells are stained with non-toxic dyes. Cells are followed over time
to see where they migrate and what they become. Early embryologists applied non-toxic, visible
dyes to specific cells or regions of an embryo. As development proceeded, the movement and
differentiation of these stained cells were tracked to determine their eventual fates.
2. Radioactive Labeling: Cells are marked with radioactive isotopes, then traced. The radioactive
isotope such as C14 and P32 and H3 are used to label the early blastomeres. Tritiated thymidine
labels the nuclei as it is incorporated in DNA of cells. These cells can be studied by
autoradiography which helps us to trace descendent cells of labelled and unlabelled cells. Less
common now due to safety concerns.
3. Genetic Markers: Using transgenic animals (e.g., with GFP – Green Fluorescent Protein).
Specific genes are marked, allowing tracking of cell lineage. Modern methods involve introducing
genetic markers, such as genes encoding fluorescent proteins (e.g., Green Fluorescent Protein or
GFP), into specific embryonic cells. These markers are inherited by descendant cells, enabling
precise tracking throughout development.
4. Laser Ablation: Target cells are destroyed; absence of resulting structures shows their normal
fate.
5. Chimera Formation: Combining cells from two embryos (e.g., quail and chick) to trace origins.
By combining cells from different species or genetically distinct embryos, researchers can trace
cell lineages based on species-specific or genetic markers. For example, grafting quail cells into
chick embryos has elucidated the developmental fate of various tissues.
1. Prospective Fate Map: Indicates what the cells will become based on prediction or observation.
2. Retrospective Fate Map: Based on lineage tracing; determines the origin of a differentiated
tissue by tracing back its cellular history.
1. Ectoderm: Forms skin, nervous system, eyes, and parts of the mouth.
2. Mesoderm: Forms muscles, bones, blood, heart, kidneys, and reproductive organs.
3. Endoderm: Forms lining of the digestive tract, liver, pancreas, and lungs.
Understanding Developmental Processes: Fate maps provide insights into how complex
organisms develop from a single fertilized egg, detailing the formation of tissues, organs, and
overall body plans.
Evolutionary Biology: Comparing fate maps across species sheds light on evolutionary
relationships and the conservation or divergence of developmental mechanisms.
The following presumptive areas can be discerned from the frog fate map given below.
1. There is a broad ectodermal area near animal hemisphere which forms epidermal layer of the skin.
This is known as epidermal ectoderm.
2. A relatively smaller ectodermal area below epidermal ectoderm that is called neuroectoderm which
contributes to neural tube and nervous tissue.
3. A crescent area below neuroectoderm is notochordal area which forms notochord in the later stage
of development.
4. On either side of the notochordal area are two prospective mesodermal regions.
6. At the caudal margin of the notochordal region is the prechordal plate region which gives rise to
head mesoderm.