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Related Concept Videos

Reporter Genes02:11

Reporter Genes

Reporter genes are a type of protein-coding gene that are often tagged to a gene of interest. Once inside a target cell, reporter genes usually produce visually identifiable characteristics like fluorescence and luminescence when expressed along with the gene of interest. Thus, reporter genes “report” the presence or absence of genes of interest in an organism, determine the gene expression pattern, or track the physical location of a DNA segment or protein in the cell.
Commonly used reporter...
In-vitro Mutagenesis01:16

In-vitro Mutagenesis

To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.

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Correction: Li et al. Genetic Deficiency of Hyaluronan Synthase 2 in the Developing Limb Mesenchyme Impairs Postnatal Synovial Joint Formation. <i>Biomedicines</i> 2025, <i>13</i>, 1324.

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Lentiviral Mediated Production of Transgenic Mice: A Simple and Highly Efficient Method for Direct Study of Founders
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Engineering BAC reporter gene constructs for mouse transgenesis.

Yu Fu1, Peter Maye

  • 1Department of Reconstructive Sciences, School of Dental Medicine, University of Connecticut Health Center, Farmington, CT, USA.

Methods in Molecular Biology (Clifton, N.J.)
|November 17, 2010
PubMed
Summary

Bacterial Artificial Chromosome (BAC) technology enables advanced biological research by providing large genomic DNA clones. This method simplifies creating reporter gene constructs for studying gene expression, such as in skeletal biology.

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Area of Science:

  • Genomics
  • Molecular Biology
  • Transgenic Technology

Background:

  • Genome sequencing and annotated databases facilitate identification and acquisition of Bacterial Artificial Chromosome (BAC) clones.
  • Genetic modification methods for BACs enable rapid creation of gene targeting and reporter gene constructs via bacterial homologous recombination.

Purpose of the Study:

  • To demonstrate the utility of BAC clones and bacterial recombination for generating fluorescent protein reporter transgenic mice.
  • To encourage adoption of BAC methodologies for engineering transgenic DNA constructs, challenging perceptions of complexity.

Main Methods:

  • Utilizing large genomic DNA clones housed in BAC vectors.
  • Employing bacterial recombination methods for genetic modification of BACs.
  • Generating fluorescent protein reporter transgenic mice, exemplified by the Tenascin C (TNC)-mCherry line.

Main Results:

  • BAC clones provide a more comprehensive representation of cis-regulatory elements due to their larger size, leading to more accurate endogenous gene expression studies.
  • Proficiency in generating BAC reporters has been achieved in a short period.
  • Successful generation of a Tenascin C (TNC)-mCherry transgenic reporter mouse line.

Conclusions:

  • BAC technology offers a powerful and accessible approach for creating sophisticated transgenic models for biological research.
  • BAC methodologies represent a viable and advantageous alternative to traditional molecular cloning techniques for construct engineering.
  • This work encourages broader laboratory adoption of BACs for advancing research in areas like skeletal biology.