RRC ID 83349
著者 Puig-Barbe A, Dettmann S, Nirello VD, Moor H, Azami S, Edgar BA, Varga-Weisz P, Korzelius J, de Navascués J.
タイトル A bHLH interaction code controls bipotential differentiation and self-renewal in the Drosophila gut.
ジャーナル Cell Rep
Abstract Multipotent adult stem cells balance self-renewal with differentiation into various cell types. How this balance is regulated at the transcriptional level is poorly understood. Here, we show that a network of basic helix-loop-helix (bHLH) transcription factors controls both stemness and bipotential differentiation in the Drosophila adult intestine. We find that homodimers of Daughterless (Da), a homolog of mammalian E proteins, maintain self-renewal of intestinal stem cells (ISCs), antagonizing the enteroendocrine fate promoted by heterodimers of Da and Scute (Sc; homolog of ASCL). The HLH factor Extramacrochaetae (Emc; homologous to Id proteins) promotes absorptive differentiation by titrating Da and Sc. Emc prevents the committed absorptive progenitor from dedifferentiating, underscoring the plasticity of these cells. Switching physical interaction partners in this way enables the active maintenance of stemness while priming stem cells for differentiation along two alternative fates. Such regulatory logic is likely operative in other bipotent stem cell systems.
巻・号 44(3)
ページ 115398
公開日 2025-3-14
DOI 10.1016/j.celrep.2025.115398
PII S2211-1247(25)00169-X
PMID 40089983
MeSH Animals Basic Helix-Loop-Helix Transcription Factors* / genetics Basic Helix-Loop-Helix Transcription Factors* / metabolism Cell Differentiation* Cell Self Renewal DNA-Binding Proteins Drosophila / metabolism Drosophila Proteins* / genetics Drosophila Proteins* / metabolism Drosophila melanogaster / metabolism Intestines / cytology Stem Cells / cytology Stem Cells / metabolism Transcription Factors / metabolism
IF 8.109
リソース情報
ショウジョウバエ 1007R-2 DGRC#115317