Germline Mutagenesis

Germline mutagenesis is the generation or introduction of DNA sequence changes in germ cells or their precursor cells, making variants potentially transmissible to offspring and important for understanding inheritance and genetic disease. Mutations can arise from replication errors, DNA damage, and imperfect repair, or be induced experimentally with chemical, physical, or genome-editing methods; changes established in germ-cell lineages can be inherited by subsequent generations. In genetics, researchers use germline mutagenesis to create model organisms, test gene function, trace inherited phenotypes, and study mutation rates and genome stability. The approach also informs evolutionary processes and the assessment of heritable genomic risk.

Germline Mutagenesis - Related Videos

Research

JoVE Journal - Biology

Single Oocyte Bisulfite Mutagenesis

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Cited by 14 •

2012

Bisulfite mutagenesis is the gold standard for analyzing DNA methylation. Our modified protocol allows for DNA methylation analysis at the single-cell level and was specifically designed for individual oocytes. It can also be used for cleavage-stage embryos.

Comprehensive Assessment of Germline Chemical Toxicity Using the Nematode Caenorhabditis elegans

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Cited by 11 •

2015

We describe the detailed steps of a high-throughput chemical assay in the nematode Caenorhabditis elegans used to assess germline toxicity. In this assay, disruption of germline function following chemical exposure is monitored using a fluorescent reporter specific to aneuploid embryos.

Optogenetic Random Mutagenesis Using Histone-miniSOG in C. elegans

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Cited by 6 •

2016

Genetically-encoded histone-miniSOG induces genome-wide heritable mutations in a blue light-dependent manner. This mutagenesis method is simple, fast, free of toxic chemicals, and well-suited for forward genetic screening and transgene integration.

An Introduction to Worm Lab: from Culturing Worms to Mutagenesis

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Cited by 27 •

2011

Screening for mutants with phenotypic defects is a straightforward method for identifying genes that function in a given biological process. In this article we describe how to culture free living worms (e.g., Pristionchus pacificus) in the laboratory and show two different mutagenesis methods, EMS and TMP/UV.

CRISPR/Cas9-mediated Endogenous Fluorescent Tagging of Germline-specific Genes in Caenorhabditis elegans

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2026

A CRISPR/Cas9 microinjection workflow for endogenous fluorescent tagging in the Caenorhabditis elegans germline to obtain homozygous knock-in lines for in vivo protein localization analysis.

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