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Updated: May 7, 2025

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Lineage Tracing and Clonal Analysis in Developing Cerebral Cortex Using Mosaic Analysis with Double Markers MADM
Published on: May 8, 2020
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In Vivo Clonal Analysis Using MADM with Spatiotemporal Specificity.
Yuwei Peng1,2,3, Efan Wang1,3, Zhongfu Shen1,2,3
1IDG/McGovern Institute of Brain Research, Tsinghua University, Beijing, People's Republic of China.
Methods in Molecular Biology (Clifton, N.J.)
|January 2, 2025
Summary
Mosaic analysis with double markers (MADM) enables precise lineage tracing in vivo. This study applies MADM for single-cell resolution analysis of developing mouse neocortex radial glial progenitors.
Area of Science:
- Neuroscience
- Developmental Biology
- Genetics
Background:
- Lineage tracing is crucial for understanding tissue development and cellular dynamics.
- Mosaic analysis with double markers (MADM) offers a powerful method for in vivo lineage tracing.
- Radial glial progenitors are key stem cells in the developing mammalian neocortex.
Purpose of the Study:
- To apply MADM for quantitative lineage analysis of radial glial progenitors.
- To achieve single-cell resolution in tracing progenitor cell fates.
- To investigate the developmental dynamics of the mouse neocortex.
Main Methods:
- Utilizing Cre recombinase-dependent interchromosomal recombination.
- Restoring stable expression of two fluorescent proteins in individual cells.
- Applying MADM for sparse labeling of stem and progenitor cells.
- Performing quantitative lineage analysis at single-cell resolution.
Main Results:
- MADM successfully enabled sparse labeling of individual radial glial progenitors.
- Quantitative lineage analysis provided insights into progenitor cell behavior.
- Single-cell resolution was achieved in tracing cell fates within the developing neocortex.
Conclusions:
- MADM is a valuable technique for detailed lineage analysis of neural progenitors.
- This approach facilitates a deeper understanding of neocortical development.
- Future studies can leverage MADM for complex developmental and disease investigations.
Keywords:
3D reconstructionClonal analysisInterchromosomal recombinationLineage tracingMADMSerial sectioning
