jumu

UniProt ID: Q9XTP7
Organism: Drosophila melanogaster
Review Status: DRAFT
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Gene Description

Jumu is a nuclear forkhead transcription factor and chromatin-associated regulator. It recognizes Forkhead sites in cis-regulatory DNA and controls context-dependent gene expression, including repression of the Nidogen enhancer in the embryonic heart. Its dosage affects chromatin and nucleolar organization, while its transcriptional programs regulate asymmetric cell fates, cardiac progenitor divisions and wound-responsive JAK/STAT signaling.

Existing Annotations Review

GO Term Evidence Action Reason
GO:0000785 chromatin
IDA
PMID:17412918
Genes required for mitotic spindle assembly in Drosophila S2...
ACCEPT
Summary: Jumu/DOM associates with chromosomal sites, including the chromocenter and specific euchromatic loci.
Reason: Jumu/DOM associates with chromosomal sites, including the chromocenter and specific euchromatic loci. These direct observations support the chromatin/polytene-chromosome assignments, and the dosage-dependent chromatin phenotype is consistent with an active chromatin-associated regulatory role.
Supporting Evidence:
PMID:10940625
DOM protein is accumulated in the chromocenter and, as expected from a transcription factor, is found at specific euchromatic loci.
GO:0000791 euchromatin
IDA
PMID:20213139
The winged-helix transcription factor JUMU regulates develop...
ACCEPT
Summary: Jumu/DOM associates with chromosomal sites, including the chromocenter and specific euchromatic loci.
Reason: Jumu/DOM associates with chromosomal sites, including the chromocenter and specific euchromatic loci. These direct observations support the chromatin/polytene-chromosome assignments, and the dosage-dependent chromatin phenotype is consistent with an active chromatin-associated regulatory role.
Supporting Evidence:
PMID:10940625
DOM protein is accumulated in the chromocenter and, as expected from a transcription factor, is found at specific euchromatic loci.
GO:0000976 transcription cis-regulatory region binding
IDA
PMID:22378636
Differential regulation of mesodermal gene expression by Dro...
MODIFY
Summary: Jumu recognizes sequence-specific Forkhead sites in a functional cis-regulatory enhancer.
Reason: Jumu recognizes sequence-specific Forkhead sites in a functional cis-regulatory enhancer. Cis-regulatory region sequence-specific DNA binding is more precise than the generic DNA-binding or regulatory-region-binding term.
Supporting Evidence:
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0000987 cis-regulatory region sequence-specific DNA binding
IBA
GO_REF:0000033
ACCEPT
Summary: Jumu is a forkhead transcription factor with directly characterized sequence-dependent enhancer regulation.
Reason: Jumu is a forkhead transcription factor with directly characterized sequence-dependent enhancer regulation. The primary Nidogen study shows cooperation with CHES-1-like to repress the cardiac enhancer through distinct Forkhead binding sites. This establishes regulatory DNA recognition and transcriptional control, rather than merely generic DNA association.
Supporting Evidence:
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0003677 DNA binding
IEA
GO_REF:0000104
MODIFY
Summary: Jumu recognizes sequence-specific Forkhead sites in a functional cis-regulatory enhancer.
Reason: Jumu recognizes sequence-specific Forkhead sites in a functional cis-regulatory enhancer. Cis-regulatory region sequence-specific DNA binding is more precise than the generic DNA-binding or regulatory-region-binding term.
Supporting Evidence:
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0003700 DNA-binding transcription factor activity
IBA
GO_REF:0000033
ACCEPT
Summary: Jumu is a forkhead transcription factor with directly characterized sequence-dependent enhancer regulation.
Reason: Jumu is a forkhead transcription factor with directly characterized sequence-dependent enhancer regulation. The primary Nidogen study shows cooperation with CHES-1-like to repress the cardiac enhancer through distinct Forkhead binding sites. This establishes regulatory DNA recognition and transcriptional control, rather than merely generic DNA association.
Supporting Evidence:
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0003700 DNA-binding transcription factor activity
IEA
GO_REF:0000002
ACCEPT
Summary: Jumu is a forkhead transcription factor with directly characterized sequence-dependent enhancer regulation.
Reason: Jumu is a forkhead transcription factor with directly characterized sequence-dependent enhancer regulation. The primary Nidogen study shows cooperation with CHES-1-like to repress the cardiac enhancer through distinct Forkhead binding sites. This establishes regulatory DNA recognition and transcriptional control, rather than merely generic DNA association.
Supporting Evidence:
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0005634 nucleus
IBA
GO_REF:0000033
ACCEPT
Summary: Direct microscopy places Jumu in nuclei, consistent with enhancer binding and transcriptional regulation.
Reason: Direct microscopy places Jumu in nuclei, consistent with enhancer binding and transcriptional regulation. This evidence independently supports the nuclear location also inferred phylogenetically.
Supporting Evidence:
PMID:10887088
Jumu protein shows nuclear localisation
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0005634 nucleus
IDA
PMID:10887088
Jumeaux, a novel Drosophila winged-helix family protein, is ...
ACCEPT
Summary: Direct microscopy places Jumu in nuclei, consistent with enhancer binding and transcriptional regulation.
Reason: Direct microscopy places Jumu in nuclei, consistent with enhancer binding and transcriptional regulation. This evidence independently supports the nuclear location also inferred phylogenetically.
Supporting Evidence:
PMID:10887088
Jumu protein shows nuclear localisation
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0005634 nucleus
IDA
PMID:27514026
The composition and organization of Drosophila heterochromat...
ACCEPT
Summary: Direct microscopy places Jumu in nuclei, consistent with enhancer binding and transcriptional regulation.
Reason: Direct microscopy places Jumu in nuclei, consistent with enhancer binding and transcriptional regulation. This evidence independently supports the nuclear location also inferred phylogenetically.
Supporting Evidence:
PMID:10887088
Jumu protein shows nuclear localisation
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0005634 nucleus
IEA
GO_REF:0000120
ACCEPT
Summary: Direct microscopy places Jumu in nuclei, consistent with enhancer binding and transcriptional regulation.
Reason: Direct microscopy places Jumu in nuclei, consistent with enhancer binding and transcriptional regulation. This evidence independently supports the nuclear location also inferred phylogenetically.
Supporting Evidence:
PMID:10887088
Jumu protein shows nuclear localisation
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0005700 polytene chromosome
IDA
PMID:10940625
Domina (Dom), a new Drosophila member of the FKH/WH gene fam...
ACCEPT
Summary: Jumu/DOM associates with chromosomal sites, including the chromocenter and specific euchromatic loci.
Reason: Jumu/DOM associates with chromosomal sites, including the chromocenter and specific euchromatic loci. These direct observations support the chromatin/polytene-chromosome assignments, and the dosage-dependent chromatin phenotype is consistent with an active chromatin-associated regulatory role.
Supporting Evidence:
PMID:10940625
DOM protein is accumulated in the chromocenter and, as expected from a transcription factor, is found at specific euchromatic loci.
GO:0005701 polytene chromosome chromocenter
IDA
PMID:10940625
Domina (Dom), a new Drosophila member of the FKH/WH gene fam...
ACCEPT
Summary: Jumu/DOM associates with chromosomal sites, including the chromocenter and specific euchromatic loci.
Reason: Jumu/DOM associates with chromosomal sites, including the chromocenter and specific euchromatic loci. These direct observations support the chromatin/polytene-chromosome assignments, and the dosage-dependent chromatin phenotype is consistent with an active chromatin-associated regulatory role.
Supporting Evidence:
PMID:10940625
DOM protein is accumulated in the chromocenter and, as expected from a transcription factor, is found at specific euchromatic loci.
GO:0005701 polytene chromosome chromocenter
IDA
PMID:20213139
The winged-helix transcription factor JUMU regulates develop...
ACCEPT
Summary: Jumu/DOM associates with chromosomal sites, including the chromocenter and specific euchromatic loci.
Reason: Jumu/DOM associates with chromosomal sites, including the chromocenter and specific euchromatic loci. These direct observations support the chromatin/polytene-chromosome assignments, and the dosage-dependent chromatin phenotype is consistent with an active chromatin-associated regulatory role.
Supporting Evidence:
PMID:10940625
DOM protein is accumulated in the chromocenter and, as expected from a transcription factor, is found at specific euchromatic loci.
GO:0005730 nucleolus
IDA
PMID:10940625
Domina (Dom), a new Drosophila member of the FKH/WH gene fam...
KEEP AS NON CORE
Summary: Jumu has an observed nucleolar pool and its dosage affects nucleolar integrity.
Reason: Jumu has an observed nucleolar pool and its dosage affects nucleolar integrity. This additional nuclear localization is supported, but the best defined molecular function is sequence-specific transcriptional regulation.
Supporting Evidence:
PMID:20213139
The correct gene dose of jumu is required for nucleolar integrity and correct nucleolus function.
PMID:20213139
displacement of the JUMU protein from the chromocenter and the nucleolus
GO:0005730 nucleolus
IDA
PMID:20213139
The winged-helix transcription factor JUMU regulates develop...
KEEP AS NON CORE
Summary: Jumu has an observed nucleolar pool and its dosage affects nucleolar integrity.
Reason: Jumu has an observed nucleolar pool and its dosage affects nucleolar integrity. This additional nuclear localization is supported, but the best defined molecular function is sequence-specific transcriptional regulation.
Supporting Evidence:
PMID:20213139
The correct gene dose of jumu is required for nucleolar integrity and correct nucleolus function.
PMID:20213139
displacement of the JUMU protein from the chromocenter and the nucleolus
GO:0006325 chromatin organization
IMP
PMID:20213139
The winged-helix transcription factor JUMU regulates develop...
ACCEPT
Summary: Jumu dosage affects chromatin organization and position-effect variegation.
Reason: Jumu dosage affects chromatin organization and position-effect variegation. Overexpression changes euchromatic chromosome arms and the chromocenter, connecting this chromatin-associated transcription factor to chromosome organization.
Supporting Evidence:
PMID:20213139
Overexpression of jumu results in bloating of euchromatic chromosome arms, displacement of the JUMU protein from the chromocenter and the nucleolus, fragile weak points, and disrupted chromocenter of polytene chromosomes.
GO:0006355 regulation of DNA-templated transcription
IBA
GO_REF:0000033
ACCEPT
Summary: Jumu is a forkhead transcription factor with directly characterized sequence-dependent enhancer regulation.
Reason: Jumu is a forkhead transcription factor with directly characterized sequence-dependent enhancer regulation. The primary Nidogen study shows cooperation with CHES-1-like to repress the cardiac enhancer through distinct Forkhead binding sites. This establishes regulatory DNA recognition and transcriptional control, rather than merely generic DNA association.
Supporting Evidence:
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0006355 regulation of DNA-templated transcription
IEA
GO_REF:0000002
ACCEPT
Summary: Jumu is a forkhead transcription factor with directly characterized sequence-dependent enhancer regulation.
Reason: Jumu is a forkhead transcription factor with directly characterized sequence-dependent enhancer regulation. The primary Nidogen study shows cooperation with CHES-1-like to repress the cardiac enhancer through distinct Forkhead binding sites. This establishes regulatory DNA recognition and transcriptional control, rather than merely generic DNA association.
Supporting Evidence:
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0007000 nucleolus organization
IMP
PMID:20213139
The winged-helix transcription factor JUMU regulates develop...
KEEP AS NON CORE
Summary: Correct Jumu dosage is required for nucleolar integrity, and overexpression of its acidic C terminus disrupts the nucleolus.
Reason: Correct Jumu dosage is required for nucleolar integrity, and overexpression of its acidic C terminus disrupts the nucleolus. This supported phenotype does not establish a distinct ribosome-processing catalytic function.
Supporting Evidence:
PMID:20213139
The correct gene dose of jumu is required for nucleolar integrity and correct nucleolus function.
GO:0007391 dorsal closure
TAS
PMID:12147138
Signaling pathways directing the movement and fusion of epit...
UNDECIDED
Summary: The dorsal-closure annotation cites a review whose cached abstract describes the general epithelial-fusion signaling network but does not resolve the Jumu-specific evidence.
Reason: The dorsal-closure annotation cites a review whose cached abstract describes the general epithelial-fusion signaling network but does not resolve the Jumu-specific evidence. A target-specific primary result or the relevant full-text passage is needed to assess this particular developmental role.
GO:0007476 imaginal disc-derived wing morphogenesis
IMP
PMID:10940625
Domina (Dom), a new Drosophila member of the FKH/WH gene fam...
KEEP AS NON CORE
Summary: Jumu/DOM mutants have rough eyes and wing-shape/margin defects, supporting these developmental roles.
Reason: Jumu/DOM mutants have rough eyes and wing-shape/margin defects, supporting these developmental roles. They are downstream tissue outcomes of a pleiotropic transcription and chromatin regulator rather than separate molecular activities.
Supporting Evidence:
PMID:10940625
Homozygous mutants show rough eyes, irregular arrangement of bristles, extended wings, defective posterior wing margins
GO:0009611 response to wounding
IMP
PMID:34999256
Jumu is required for the activation of JAK/STAT in Drosophil...
KEEP AS NON CORE
Summary: Jumu is required for wound-induced JAK/STAT activation and lymph-gland signaling.
Reason: Jumu is required for wound-induced JAK/STAT activation and lymph-gland signaling. This establishes a regulatory role upstream of the pathway under tissue-damage conditions, without implying that Jumu itself is a kinase or wound sensor.
Supporting Evidence:
PMID:34999256
Jumu is required for the activation of JAK/STAT in response to epidermal wounds.
GO:0035050 embryonic heart tube development
IMP
PMID:22814603
Two forkhead transcription factors regulate the division of ...
KEEP AS NON CORE
Summary: Jumu and CHES-1-like regulate symmetric and asymmetric cardiac-progenitor divisions through Polo activity.
Reason: Jumu and CHES-1-like regulate symmetric and asymmetric cardiac-progenitor divisions through Polo activity. The genetic data support heart development and division control as specific biological consequences of their transcriptional program.
Supporting Evidence:
PMID:22814603
jumu and CHES-1-like control the division of cardiac progenitors by regulating the activity of Polo
GO:0043565 sequence-specific DNA binding
IEA
GO_REF:0000002
MODIFY
Summary: Jumu recognizes sequence-specific Forkhead sites in a functional cis-regulatory enhancer.
Reason: Jumu recognizes sequence-specific Forkhead sites in a functional cis-regulatory enhancer. Cis-regulatory region sequence-specific DNA binding is more precise than the generic DNA-binding or regulatory-region-binding term.
Supporting Evidence:
PMID:22378636
CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
PMID:22378636
different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
GO:0046427 positive regulation of receptor signaling pathway via JAK-STAT
IMP
PMID:34999256
Jumu is required for the activation of JAK/STAT in Drosophil...
KEEP AS NON CORE
Summary: Jumu is required for wound-induced JAK/STAT activation and lymph-gland signaling.
Reason: Jumu is required for wound-induced JAK/STAT activation and lymph-gland signaling. This establishes a regulatory role upstream of the pathway under tissue-damage conditions, without implying that Jumu itself is a kinase or wound sensor.
Supporting Evidence:
PMID:34999256
Jumu is required for the activation of JAK/STAT in response to epidermal wounds.
GO:0048749 compound eye development
IMP
PMID:10940625
Domina (Dom), a new Drosophila member of the FKH/WH gene fam...
KEEP AS NON CORE
Summary: Jumu/DOM mutants have rough eyes and wing-shape/margin defects, supporting these developmental roles.
Reason: Jumu/DOM mutants have rough eyes and wing-shape/margin defects, supporting these developmental roles. They are downstream tissue outcomes of a pleiotropic transcription and chromatin regulator rather than separate molecular activities.
Supporting Evidence:
PMID:10940625
Homozygous mutants show rough eyes, irregular arrangement of bristles, extended wings, defective posterior wing margins
GO:0051302 regulation of cell division
IMP
PMID:22814603
Two forkhead transcription factors regulate the division of ...
KEEP AS NON CORE
Summary: Jumu and CHES-1-like regulate symmetric and asymmetric cardiac-progenitor divisions through Polo activity.
Reason: Jumu and CHES-1-like regulate symmetric and asymmetric cardiac-progenitor divisions through Polo activity. The genetic data support heart development and division control as specific biological consequences of their transcriptional program.
Supporting Evidence:
PMID:22814603
jumu and CHES-1-like control the division of cardiac progenitors by regulating the activity of Polo

Core Functions

Regulates gene expression by recognizing Forkhead sites in cis-regulatory DNA.

Supporting Evidence:
  • PMID:22378636
    CHES-1-like cooperates with Jumu to repress this enhancer in the heart.
  • PMID:22378636
    different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF.
  • PMID:10887088
    Jumu protein shows nuclear localisation

References

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External Prediction Reviews

These computational predictions are reviewed separately from the GOA annotation set used for this review. The assessments below are from this project and do not constitute official GO annotations or endorsement by GO/UniProt. They are not included in the existing annotation review above.

ProtNLM2 External predictions

View prediction review YAML Β· jumu-protnlm-predictions-review.yaml Β· Review status: COMPLETE

The DNA-binding prediction is supported but less precise than the directly characterized sequence-specific enhancer-binding function.

Source documents: projects/PROTNLM_EVALUATION/fly-benchmark/predictions.jsonl.gz Β· genes/DROME/jumu/jumu-predictions-source.json

Review score: 2 = concordant with evidence; 1 = uncertain; 0 = discordant with evidence. This is an assessment score, not a model probability.

GO:0043565 sequence-specific DNA binding GO_MF
LSP β€” Less precise than existing annotation Review score: 2/2
Prediction method: ProtNLM2 Β· Version: UniProt API snapshot 2026-09-08
Review rationale: Sequence-specific DNA binding is directly supported by the Jumu/Forkhead-site analysis of the Nidogen enhancer. Jumu cooperates with CHES-1-like in cardiac repression, with distinct binding-site combinations determining regulatory activity. The existing cis-regulatory region sequence-specific DNA-binding annotation is more informative than the broad prediction.
Supporting Evidence:
  • PMID:22378636: "CHES-1-like cooperates with Jumu to repress this enhancer in the heart."
  • PMID:22378636: "different combinations of Fkh sites, corresponding to two different sequence specificities, mediate the particular functions of each TF."

Deep Research

Falcon

(jumu-deep-research-falcon.md)

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πŸ“š Additional Documentation

Notes

(jumu-notes.md)

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πŸ“„ View Raw YAML

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