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Related Concept Videos

MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA ends...
Master Transcription Regulators02:23

Master Transcription Regulators

Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a  complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
Chromatin Structure Regulates pre-mRNA Processing02:41

Chromatin Structure Regulates pre-mRNA Processing

In eukaryotic cells, nascent mRNA transcripts need to undergo many post-transcriptional modifications to reach the cell cytoplasm and translate into functional proteins. For a long time, transcription and pre-mRNA processing were considered two independent events that occur sequentially in the cell. However, it has now been well established that transcription and pre-mRNA processing are two simultaneous processes that are precisely regulated inside the cell.
The chromatin structure, especially...
Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying DNA...
Somatic to iPS Cell Reprogramming01:29

Somatic to iPS Cell Reprogramming

Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012 for this...

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Related Experiment Video

Updated: May 26, 2026

Differentiation of a Human Neural Stem Cell Line on Three Dimensional Cultures, Analysis of MicroRNA and Putative Target Genes
10:48

Differentiation of a Human Neural Stem Cell Line on Three Dimensional Cultures, Analysis of MicroRNA and Putative Target Genes

Published on: April 12, 2015

Intronic miR-26b controls neuronal differentiation by repressing its host transcript, ctdsp2.

Holger Dill1, Bastian Linder, Alexander Fehr

  • 1Department of Biochemistry, Theodor Boveri-Institute, University of Würzburg, Würzburg, Germany.

Genes & Development
|January 5, 2012
PubMed
Summary

MicroRNA-26b (miR-26b) activates neuronal gene expression by targeting CTDSP2 phosphatases, promoting neural stem cell differentiation. This microRNA is crucial for neurogenesis and neuronal cell development.

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Last Updated: May 26, 2026

Differentiation of a Human Neural Stem Cell Line on Three Dimensional Cultures, Analysis of MicroRNA and Putative Target Genes
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Published on: April 12, 2015

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Area of Science:

  • Neuroscience
  • Molecular Biology
  • Genetics

Background:

  • Neural stem cell (NSC) differentiation into neurons is regulated by the REST/NRSF complex.
  • RNA polymerase II C-terminal domain small phosphatases (CTDSPs) are key REST/NRSF components that suppress neuronal gene expression in NSCs.
  • The precise mechanisms activating CTDSPs for neurogenesis remain unclear.

Purpose of the Study:

  • To elucidate the regulatory mechanism controlling CTDSP2 during neurogenesis.
  • To investigate the role of microRNA-26b (miR-26b) in neural stem cell differentiation.

Main Methods:

  • Analysis of the regulatory relationship between miR-26b and CTDSP2.
  • Investigating miR-26b biogenesis during neurogenesis.
  • Assessing the impact of miR-26b on Ctdsp2 protein levels and neuronal differentiation in vivo.

Main Results:

  • CTDSP2 was identified as a direct target of miR-26b.
  • miR-26b is encoded within the CTDSP2 primary transcript, forming an intrinsic feedback loop.
  • miR-26b biogenesis is inhibited in NSCs but activated during neurogenesis, leading to suppressed Ctdsp2 expression.
  • Activated miR-26b is essential for neuronal differentiation in vivo.

Conclusions:

  • A novel miR-26b/CTDSP2 negative feedback loop regulates neurogenesis.
  • miR-26b plays a critical role in suppressing CTDSP2 and promoting neuronal differentiation.
  • This mechanism is vital for the precise control of neuronal development.