Decoding anterior–posterior patterning cues into embryo-wide binary fate decisions through recruitment-mediated targeting

Developmental pattern formation requires patterning cues to be converted into discrete, gene- and cell-specific regulatory outputs, but how this conversion is achieved remains unclear. We address this problem in Caenorhabditis elegans anterior–posterior patterning, where quantitatively asymmetric Wnt/β-catenin cues, namely anterior-enriched POP-1/TCF and posterior-enriched SYS-1/β-catenin, are decoded into binary, switch-like fate decisions. We show that these cues are resolved into embryo-wide binary regulatory outputs through ZIP-7/DBP, a transcription factor with stage-specific, lineage-wide posterior-exclusive expression that is essential for multiple posterior fate decisions. We define a model for this cue-to-decision decoding. At the zip-7 promoter, the transcription factor ZIP-8/NFIL3, which begins to be expressed during mid-embryogenesis prior to ZIP-7 onset, provides an activating input while recruiting POP-1 and SYS-1. POP-1 restrains this activity anteriorly, whereas the POP-1–SYS-1 complex promotes it posteriorly, thereby generating a binary pattern of zip-7 transcription. This recruitment-mediated promoter control couples Wnt/β-catenin cues to gene-specific transcriptional regulation and enables flexible spatiotemporal control of cue-dependent transcription. Genome-wide analyses further suggest that recruitment-mediated cotargeting may extend beyond zip-7 and point to additional candidate factors with similar recruitment functions, supporting a scalable framework for decoding patterning cues into context-specific regulatory decisions.

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Publication Details

Journal
Genes & Development
Published
2026-09-01
DOI
https://doi.org/10.1101/gad.353848.126
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
preprint

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preprint

Decoding anterior–posterior patterning cues into embryo-wide binary fate decisions through recruitment-mediated targeting

Huan Qi, Zhuo Du, Xuehua Ma, Zixin Zhou et al.
Genes & Development
Genetics, Aging, and Longevity in Model Organisms
preprint

Decoding anterior–posterior patterning cues into embryo-wide binary fate decisions through recruitment-mediated targeting

Huan Qi, Zhuo Du, Xuehua Ma, Zixin Zhou, Yulin Cong, Long Xiao, Yuchuan Bai, Yingchun Wang, Xiahe Huang
preprint en

Abstract

Developmental pattern formation requires patterning cues to be converted into discrete, gene- and cell-specific regulatory outputs, but how this conversion is achieved remains unclear. We address this problem in Caenorhabditis elegans anterior–posterior patterning, where quantitatively asymmetric Wnt/β-catenin cues, namely anterior-enriched POP-1/TCF and posterior-enriched SYS-1/β-catenin, are decoded into binary, switch-like fate decisions. We show that these cues are resolved into embryo-wide binary regulatory outputs through ZIP-7/DBP, a transcription factor with stage-specific, lineage-wide posterior-exclusive expression that is essential for multiple posterior fate decisions. We define a model for this cue-to-decision decoding. At the zip-7 promoter, the transcription factor ZIP-8/NFIL3, which begins to be expressed during mid-embryogenesis prior to ZIP-7 onset, provides an activating input while recruiting POP-1 and SYS-1. POP-1 restrains this activity anteriorly, whereas the POP-1–SYS-1 complex promotes it posteriorly, thereby generating a binary pattern of zip-7 transcription. This recruitment-mediated promoter control couples Wnt/β-catenin cues to gene-specific transcriptional regulation and enables flexible spatiotemporal control of cue-dependent transcription. Genome-wide analyses further suggest that recruitment-mediated cotargeting may extend beyond zip-7 and point to additional candidate factors with similar recruitment functions, supporting a scalable framework for decoding patterning cues into context-specific regulatory decisions.

Genes & Development
Yunnan University (CN), Chinese Academy of Sciences (CN), Institute of Genetics and Developmental Biology (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Peace, Justice and strong institutions
Genetics, Aging, and Longevity in Model Organisms
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