Temporal induction of the homeodomain transcription factor Nkx2-1 is sufficient to respecify foregut and hindgut endoderm to a pulmonary fate in Xenopus laevis

The ability of transcription factors (TFs) to regulate cell fate decisions is paramount in developmental, homeostatic, and pathogenic contexts. The homeodomain TF NKX2-1 is an essential and evolutionarily conserved master regulator of pulmonary fate in vertebrates. In this study, we tested the spatial-temporal ability of Xenopus and Human NKX2-1 to respecify foregut and hindgut endoderm in developing <i>Xenopus laevis</i> embryos into a pulmonary fate, as indicated by expression of pulmonary surfactant genes <i>sftpc</i> and <i>sftpb</i> . Interestingly, we find that both Human and Xenopus NKX2-1 can induce the ectopic expression of pulmonary surfactant genes in foregut and hindgut endoderm over a wide range of developmental times, as well as suppress the expression of midgut and hindgut specific genes. These results suggest a single pulmonary TF can reprogram developing endoderm and specify pulmonary fate. In addition, our work provides a comparative platform for future studies investigating how mutations in Human <i>NKX2-1</i> may affect its transcriptional activity.

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Journal
PubMed
Published
2025-04-21
DOI
https://doi.org/10.17912/micropub.biology.001610
Primary Topic
Neonatal Respiratory Health Research
Type
article
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article

Temporal induction of the homeodomain transcription factor Nkx2-1 is sufficient to respecify foregut and hindgut endoderm to a pulmonary fate in Xenopus laevis

Aaron M. Zorn, Emma K. Lundberg, Scott A. Rankin, Brian A. Hyatt et al.
PubMed
Neonatal Respiratory Health Research
article

Temporal induction of the homeodomain transcription factor Nkx2-1 is sufficient to respecify foregut and hindgut endoderm to a pulmonary fate in Xenopus laevis

Aaron M. Zorn, Emma K. Lundberg, Scott A. Rankin, Brian A. Hyatt, Rachael Eye
article en

Abstract

The ability of transcription factors (TFs) to regulate cell fate decisions is paramount in developmental, homeostatic, and pathogenic contexts. The homeodomain TF NKX2-1 is an essential and evolutionarily conserved master regulator of pulmonary fate in vertebrates. In this study, we tested the spatial-temporal ability of Xenopus and Human NKX2-1 to respecify foregut and hindgut endoderm in developing <i>Xenopus laevis</i> embryos into a pulmonary fate, as indicated by expression of pulmonary surfactant genes <i>sftpc</i> and <i>sftpb</i> . Interestingly, we find that both Human and Xenopus NKX2-1 can induce the ectopic expression of pulmonary surfactant genes in foregut and hindgut endoderm over a wide range of developmental times, as well as suppress the expression of midgut and hindgut specific genes. These results suggest a single pulmonary TF can reprogram developing endoderm and specify pulmonary fate. In addition, our work provides a comparative platform for future studies investigating how mutations in Human <i>NKX2-1</i> may affect its transcriptional activity.

PubMedVol. 2025
Bethel University (US)
Openalex Percentile: Top 81%
Neonatal Respiratory Health Research
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