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Protocol for mapping cell lineage and cell-type identity of clonally-related cells in situ using MADM-CloneSeq.
Cheung, Giselle; Pauler, Florian M; Koppensteiner, Peter; Hippenmeyer, Simon.
Affiliation
  • Cheung G; Institute of Science and Technology Austria (ISTA), Am Campus 1, 3400 Klosterneuburg, Austria.
  • Pauler FM; Institute of Science and Technology Austria (ISTA), Am Campus 1, 3400 Klosterneuburg, Austria.
  • Koppensteiner P; Institute of Science and Technology Austria (ISTA), Am Campus 1, 3400 Klosterneuburg, Austria.
  • Hippenmeyer S; Institute of Science and Technology Austria (ISTA), Am Campus 1, 3400 Klosterneuburg, Austria. Electronic address: simon.hippenmeyer@ist.ac.at.
STAR Protoc ; 5(3): 103168, 2024 Sep 20.
Article in En | MEDLINE | ID: mdl-38968076
ABSTRACT
The lineage relationship of clonally-related cells offers important insights into the ontogeny and cytoarchitecture of the brain in health and disease. Here, we provide a protocol to concurrently assess cell lineage relationship and cell-type identity among clonally-related cells in situ. We first describe the preparation and screening of acute brain slices containing clonally-related cells labeled using mosaic analysis with double markers (MADM). We then outline steps to collect RNA from individual cells for downstream applications and cell-type identification using RNA sequencing. For complete details on the use and execution of this protocol, please refer to Cheung et al.1.
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Full text: 1 Database: MEDLINE Main subject: Brain / Cell Lineage Limits: Animals Language: En Journal: STAR Protoc / STAR protocols Year: 2024 Type: Article Affiliation country: Austria

Full text: 1 Database: MEDLINE Main subject: Brain / Cell Lineage Limits: Animals Language: En Journal: STAR Protoc / STAR protocols Year: 2024 Type: Article Affiliation country: Austria