4.8 Article

Helios is a key transcriptional regulator of outer hair cell maturation

Journal

NATURE
Volume 563, Issue 7733, Pages 696-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41586-018-0728-4

Keywords

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Funding

  1. Action on Hearing Loss [G65]
  2. Medical Research Council [MC_U142684175]
  3. Wellcome Trust [102892]
  4. NIDCD/NIH [R01DC013817, R01DC03544, T32DC00046, F31DC016218, R01DC014658]
  5. DOD CDMRP [MR130240]
  6. Intramural Program at NIDCD [DC000059]
  7. MRC [MC_U142684175, MC_UP_1503/2, MC_UP_1502/1] Funding Source: UKRI
  8. NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS [R01DC013817, ZIADC000059, R01DC003544, F31DC016218, R01DC014658, T32DC000046] Funding Source: NIH RePORTER

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The sensory cells that are responsible for hearing include the cochlear inner hair cells (IHCs) and outer hair cells (OHCs), with the OHCs being necessary for sound sensitivity and tuning(1). Both cell types are thought to arise from common progenitors; however, our understanding of the factors that control the fate of IHCs and OHCs remains limited. Here we identify Ikzf2 (which encodes Helios) as an essential transcription factor in mice that is required for OHC functional maturation and hearing. Helios is expressed in postnatal mouse OHCs, and in the cello mouse model a point mutation in Ikzf2 causes early-onset sensorineural hearing loss. Ikzf2(cello/cello) OHCs have greatly reduced prestin-dependent electromotile activity, a hallmark of OHC functional maturation, and show reduced levels of crucial OHC-expressed genes such as Slc26a5 (which encodes prestin) and Ocm. Moreover, we show that ectopic expression of Ikzf2 in IHCs: induces the expression of OHC-specific genes; reduces the expression of canonical IHC genes; and confers electromotility to IHCs, demonstrating that Ikzf2 can partially shift the IHC transcriptome towards an OHC-like identity.

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