Insertion of Inhbb into the Inhba locus rescues the Inhba-null phenotype and reveals new activin functions

Chester W. Brown, Dianne E. Houston-Hawkins, Teresa K. Woodruff, Martin M. Matzuk*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

158 Scopus citations

Abstract

The activins (dimers of βA or βB subunits, encoded by the genes Inhba and Inhbb, respectively) are TGF-β superfamily members that have roles in reproduction and development1-3. Whereas mice homozygous for the Inhba-null allele demonstrate disruption of whisker, palate and tooth development, leading to neonatal lethality4,5, homozygous Inhbb-null mice are viable, fertile and have eye defects6,7. To determine if these phenotypes were due to spatiotemporal expression differences of the ligands or disruption of specific ligand-receptor interactions, we replaced the region of Inhba encoding the mature protein with Inhbb, creating the allele Inhbatm2Zuk (hereafter designated InhbaBK). Although the craniofacial phenotypes of the Inhba-null mutation were rescued by the InhbaBK allele, somatic, testicular, genital and hair growth were grossly affected and influenced by the dosage and bioactivity of the allele. Thus, functional compensation within the TGF-β superfamily can occur if the replacement gene is expressed appropriately. The novel phenotypes in these mice further illustrate the usefulness of insertion strategies for defining protein function.

Original languageEnglish (US)
Pages (from-to)453-457
Number of pages5
JournalNature Genetics
Volume25
Issue number4
DOIs
StatePublished - 2000

ASJC Scopus subject areas

  • Genetics

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