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Related Concept Videos

Forced Transdifferentiation01:28

Forced Transdifferentiation

Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
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Methods of Nuclear Reprogramming

Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for injury repair.
Introduction to Nuclear Reprogramming01:14

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Nuclear reprogramming is the process of switching gene expression of one cell type to that of another cell type, usually from a differentiated cell state to an undifferentiated cell state. Differentiation occurs during processes such as development and morphogenesis, tissue regeneration, and malignancy. Cells can also be artificially induced to reprogram their gene expression by techniques such as nuclear transfer, induced pluripotency, and cell fusion. Such techniques have many applications in...
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Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
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Epigenetic Regulation

Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
Epigenetic Regulation01:37

Epigenetic Regulation

Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
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Paramutation at the maize pl1 locus is associated with RdDM activity at distal tandem repeats.

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Paramutation: a process for acquiring trans-generational regulatory states.

Karl F Erhard1, Jay B Hollick

  • 1Department of Plant and Microbial Biology, University of California, Berkeley, CA 94720-3102, USA.

Current Opinion in Plant Biology
|March 23, 2011
PubMed
Summary

Paramutations, which alter gene regulation and phenotype, involve trans-homolog interactions. Small interfering RNAs (siRNAs) and chromatin changes are crucial for maintaining these heritable epigenetic states in maize.

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Area of Science:

  • Epigenetics
  • Molecular Biology
  • Plant Genetics

Background:

  • Paramutations challenge Mendelian inheritance by causing heritable changes in gene regulation and phenotype through trans-homolog interactions.
  • These phenomena, initially observed in plants, are now recognized across diverse eukaryotic organisms.

Purpose of the Study:

  • To investigate the molecular mechanisms underlying paramutation in maize.
  • To determine the role of small interfering RNA (siRNA) biogenesis pathways in maintaining heritable regulatory states.

Main Methods:

  • Genetic and molecular analyses of paramutation in maize.
  • Examination of the involvement of siRNA pathways and chromatin modifications.

Main Results:

  • Components of the siRNA biogenesis pathway are essential for maintaining meiotically heritable regulatory states in maize.
  • Evidence suggests that siRNAs alone are insufficient to mediate paramutation, with transcription of associated repeats and siRNA-facilitated chromatin changes also playing key roles.

Conclusions:

  • Paramutation involves complex interactions beyond siRNAs alone.
  • Heritable epigenetic changes in paramutation are directed and maintained by transcriptional activity of repeats and siRNA-guided chromatin alterations.