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Related Concept Videos

Pleiotropy01:33

Pleiotropy

Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
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The cochlea is a coiled structure in the inner ear that contains hair cells—the sensory receptors of the auditory system. Sound waves are transmitted to the cochlea by small bones attached to the eardrum called the ossicles, which vibrate the oval window that leads to the inner ear. This causes fluid in the chambers of the cochlea to move, vibrating the basilar membrane.
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Auditory sensation, commonly called hearing, involves the transformation of sonic waves into neural impulses facilitated by the structures of the auditory organ. The prominent, flesh-like structure on the side of the head, called the auricle, directs sound waves towards the auditory canal. The auricle is often mislabeled as the pinna, a term more aligned with mobile structures like a feline's external ear. The auditory canal penetrates the cranium via the external auditory meatus of the...

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Initiating Differentiation in Immortalized Multipotent Otic Progenitor Cells
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Expression and function of Sox21 during mouse cochlea development.

Makoto Hosoya1, Masato Fujioka, Satoru Matsuda

  • 1Department of Physiology, School of Medicine, Keio University, Tokyo, Japan.

Neurochemical Research
|February 3, 2011
PubMed
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Sox21 is crucial for inner ear development, specifically in supporting cells near hair cells. Sox21-deficient mice show mild hearing loss and altered hair cell polarity, suggesting a role in fine-tuning cell fate.

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Area of Science:

  • Developmental Biology
  • Genetics
  • Neuroscience

Background:

  • Inner ear development involves precise cell-type generation.
  • Sox gene family members are critical for cell-fate determination in the inner ear.

Purpose of the Study:

  • To investigate the expression pattern of Sox21 in the developing and adult murine cochlea.
  • To understand the role of Sox21 in inner ear development and function.

Main Methods:

  • Analysis of Sox21 expression during murine cochlear development.
  • Auditory brainstem response testing in Sox21 knockout mice.

Main Results:

  • Sox21 expression shifts from widespread in early development to specific supporting cells in adults.
  • Sox21 knockout mice exhibit mild hearing impairments and defects in hair cell planar cell polarity.
  • Sox21 is expressed in supporting cells adjacent to hair cells.

Conclusions:

  • Sox21 plays a role in refining cell fate decisions during inner ear development.
  • Sox21 acts as a counteracting partner to SoxB1 family members.
  • Sox21 expression patterns can identify specific supporting cell populations.