FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Gene: Dmel\polo
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General Information
Symbol
Dmel\polo
Species
D. melanogaster
Name
polo
Annotation Symbol
CG12306
Feature Type
FlyBase ID
FBgn0003124
Gene Model Status
Stock Availability
Enzyme Name (EC)
Gene Summary
May play a role in regulating both nuclear and cytoplasmic aspects of the mitotic cycle (PubMed:1660828). Regulates localization of the augmin complex during mitosis by ensuring its location on mitotic spindles (PubMed:24829288). Also regulates augmin complex localization during male meiosis by promoting its placement at kinetochores while preventing its association with spindle microtubules (PubMed:24829288). (UniProt, P52304)
Contribute a Gene Snapshot for this gene.
Also Known As

Polo kinase, l(3)01673, Plk1, l(3)77Aa

Key Links
Genomic Location
Cytogenetic map
Sequence location
Recombination map
3-47
RefSeq locus
NT_037436 REGION:20309654..20313466
Sequence
Genomic Maps
Other Genome Views
The following external sites may use different assemblies or annotations than FlyBase.
Function
Gene Ontology (GO) Annotations (39 terms)
Molecular Function (4 terms)
Terms Based on Experimental Evidence (3 terms)
CV Term
Evidence
References
Terms Based on Predictions or Assertions (3 terms)
CV Term
Evidence
References
enables ATP binding
inferred from electronic annotation with InterPro:IPR000719
Biological Process (21 terms)
Terms Based on Experimental Evidence (20 terms)
CV Term
Evidence
References
inferred from mutant phenotype
inferred from mutant phenotype
involved_in centrosome cycle
inferred from mutant phenotype
inferred from mutant phenotype
involved_in female meiosis II
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
involved_in mitotic cell cycle
inferred from mutant phenotype
inferred from genetic interaction with FLYBASE:Map205; FB:FBgn0002645
inferred from high throughput mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
involved_in pronuclear fusion
inferred from mutant phenotype
inferred from mutant phenotype
inferred from mutant phenotype
Terms Based on Predictions or Assertions (1 term)
CV Term
Evidence
References
inferred from biological aspect of ancestor with PANTHER:PTN000679870
Cellular Component (14 terms)
Terms Based on Experimental Evidence (14 terms)
CV Term
Evidence
References
located_in centriole
inferred from direct assay
located_in cytoplasm
inferred from direct assay
located_in cytosol
inferred from direct assay
inferred from direct assay
located_in microtubule
inferred from direct assay
inferred from direct assay
located_in nuclear envelope
inferred from direct assay
is_active_in nucleus
inferred from direct assay
inferred from direct assay
located_in spindle pole
inferred from direct assay
Terms Based on Predictions or Assertions (5 terms)
CV Term
Evidence
References
is_active_in centrosome
inferred from biological aspect of ancestor with PANTHER:PTN008613836
is_active_in cytoplasm
inferred from biological aspect of ancestor with PANTHER:PTN000679870
is_active_in kinetochore
inferred from biological aspect of ancestor with PANTHER:PTN000679870
is_active_in nucleus
inferred from biological aspect of ancestor with PANTHER:PTN007795324
is_active_in spindle pole
inferred from biological aspect of ancestor with PANTHER:PTN000679870
Protein Family (UniProt)
Belongs to the protein kinase superfamily. Ser/Thr protein kinase family. CDC5/Polo subfamily. (P52304)
Catalytic Activity (EC/Rhea)
protein serine/threonine kinase activity
Summaries
Gene Group (FlyBase)
UNCLASSIFIED CONVENTIONAL PROTEIN KINASE DOMAIN KINASES -
This group comprises conventional protein kinase domain kinases that do not classify under other groups in FlyBase.
Protein Function (UniProtKB)
May play a role in regulating both nuclear and cytoplasmic aspects of the mitotic cycle (PubMed:1660828). Regulates localization of the augmin complex during mitosis by ensuring its location on mitotic spindles (PubMed:24829288). Also regulates augmin complex localization during male meiosis by promoting its placement at kinetochores while preventing its association with spindle microtubules (PubMed:24829288).
(UniProt, P52304)
Phenotypic Description (Red Book; Lindsley and Zimm 1992)
polo: polo
Maternal-effect mitotic mutation and male meiotic mutation. The wild type allele functions in the early embryo and in the imaginal and neuroblast cells of the larva. About 7% of polo1 homozygotes (offspring of polo1/+ females mated to polo1/+ or polo1/polo1 males) survive to adulthood, but most of them die as late third instar larvae, their imaginal disks and neuroblast cells failing to proliferate. polo2 homozygotes (offspring of polo2/+ females mated to polo2/+ males) never eclose, dying as early third-instar larvae. Some polo1/polo2 heterozygotes (less than 7%) survive, but show very abnormal cuticle formation in the abdominal tergites. Offspring of surviving polo1/polo1 females die very early in development, the embryos showing an abnormal distribution of nuclei that fail to cellularize and then become polyploid before breaking down. Spindles of these embryonic nuclei are highly branched and have broad, barrel-shaped poles. In third instar larvae homozygous for polo1, many of the neuroblast cells show mitotic abnormalities. In anaphase, the chromosomes are often in a circular arrangement and may or may not be polyploid or aneuploid; these chromosomes, however, are never fragmented and seem to undergo normal condensation. In anaphase, chromosomes frequently lie in a random orientation at one or both poles. Surviving polo1/polo1 males are fertile, but often show meiotic abnormalities. Many of the meiotic spindles are irregular in shape and structure amd a high frequency of nondisjunction occurs, mostly in the second meiotic division.
Summary (Interactive Fly)

protein kinase - regulates mitosis - participates in the control of mitotic progression by targeting Cdc25/String - centrosome-specific phosphorylation of Cnn by Polo/Plk1 drives Cnn scaffold assembly and centrosome maturation - Cdk1 phosphorylates Sas-4 to recruit Polo to daughter centrioles and convert them to centrosomes

Gene Model and Products
Number of Transcripts
2
Number of Unique Polypeptides
1

Please see the JBrowse view of Dmel\polo for information on other features

To submit a correction to a gene model please use the Contact FlyBase form

Protein Domains (via Pfam)
Isoform displayed:
Pfam protein domains
InterPro name
classification
start
end
Protein Domains (via SMART)
Isoform displayed:
SMART protein domains
InterPro name
classification
start
end
Structure
Protein 3D structure   (Predicted by AlphaFold)   (AlphaFold entry P52304)

If you don't see a structure in the viewer, refresh your browser.
Model Confidence:
  • Very high (pLDDT > 90)
  • Confident (90 > pLDDT > 70)
  • Low (70 > pLDDT > 50)
  • Very low (pLDDT < 50)

AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.

Experimentally Determined Structures
Crossreferences
Comments on Gene Model

Low-frequency RNA-Seq exon junction(s) not annotated.

Gene model reviewed during 5.45

Transcript Data
Annotated Transcripts
Name
FlyBase ID
RefSeq ID
Length (nt)
Assoc. CDS (aa)
FBtr0074839
2980
576
FBtr0100318
2324
576
Additional Transcript Data and Comments
Reported size (kB)

2.5, 2.2 (northern blot)

Comments
External Data
Crossreferences
Polypeptide Data
Annotated Polypeptides
Name
FlyBase ID
Predicted MW (kDa)
Length (aa)
Theoretical pI
UniProt
RefSeq ID
GenBank
FBpp0074608
67.0
576
9.19
FBpp0099722
67.0
576
9.19
Polypeptides with Identical Sequences

The group(s) of polypeptides indicated below share identical sequence to each other.

576 aa isoforms: polo-PA, polo-PB
Additional Polypeptide Data and Comments
Reported size (kDa)

576 (aa); 65 (kD observed)

Comments

A GFP-polo construct was used as a marker for centrosomes,mitotic spindles, kinetochores, and the midbody during early embryogenesis.

External Data
Linkouts
Sequences Consistent with the Gene Model
Nucleotide / Polypeptide Records
 
Mapped Features

Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\polo using the Feature Mapper tool.

External Data
Crossreferences
Eukaryotic Promoter Database - A collection of databases of experimentally validated promoters for selected model organisms.
Linkouts
Expression Data
Testis-specificity index

The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).

0.57

Transcript Expression
in situ
Stage
Tissue/Position (including subcellular localization)
Reference
northern blot
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data

polo transcripts are present throughout development and are particularly abundant in early embryos and adult females. They are observed throuhgout the syncytial embryo and in a cortical layer in the blastoderm embryo by in situ hybridization. Following cellularization, the polo transcript distribution broadly correlates with regions of the embyro undergoing divisions. polo transcripts are also found in larval tissues containing diploid cells such as testis, imaginal discs, and brain. Within these, expression is strongest in cells undergoing proliferation. In the brain, these include the proliferating centers in the optic lobes and the parts of the ventral ganglion giving rise to thoracic innervation.

Marker for
 
Subcellular Localization
CV Term
Polypeptide Expression
distribution deduced from reporter or direct label
Stage
Tissue/Position (including subcellular localization)
Reference
immunolocalization
Stage
Tissue/Position (including subcellular localization)
Reference
Additional Descriptive Data

polo protein is present at low levels in the oocyte until stage S11 or S12 after which it fills the oocyte cytoplasm from stage S12 to S13 on.

polo protein localizes to the kinetochore at nuclear envelope breakdown.

polo protein localizes at centrosomes early in mitosis and simultaneously, some staining is associated with metaphase chromosomes. Centrosome staining is progressively lost during anaphse-telophase with a concurrent increase in midbody staining. By the end of telophase, staining is only found in the midbody.

Marker for
Subcellular Localization
CV Term
Evidence
References
located_in centriole
inferred from direct assay
located_in cytoplasm
inferred from direct assay
located_in cytosol
inferred from direct assay
inferred from direct assay
located_in microtubule
inferred from direct assay
inferred from direct assay
located_in nuclear envelope
inferred from direct assay
is_active_in nucleus
inferred from direct assay
inferred from direct assay
located_in spindle pole
inferred from direct assay
Expression Deduced from Reporters
High-Throughput Expression Data
Associated Tools

JBrowse - Visual display of RNA-Seq signals

View Dmel\polo in JBrowse
RNA-Seq by Region - Search RNA-Seq expression levels by exon or genomic region
Reference
See Gelbart and Emmert, 2013 for analysis details and data files for all genes.
Developmental Proteome: Life Cycle
Developmental Proteome: Embryogenesis
External Data and Images
Linkouts
DRscDB - A single-cell RNA-seq resource for data mining and data comparison across species
EMBL-EBI Single Cell Expression Atlas - Single cell expression across species
FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
FlyAtlas2 - A Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data
Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
Flygut - An atlas of the Drosophila adult midgut
Images
Alleles, Insertions, Transgenic Constructs, and Aberrations
Classical and Insertion Alleles ( 32 )
For All Classical and Insertion Alleles Show
 
Other relevant insertions
Transgenic Constructs ( 60 )
For All Alleles Carried on Transgenic Constructs Show
Transgenic constructs containing/affecting coding region of polo
Transgenic constructs containing regulatory region of polo
Aberrations (Deficiencies and Duplications) ( 8 )
Variants
Variant Molecular Consequences
Alleles Representing Disease-Implicated Variants
Phenotypes
For more details about a specific phenotype click on the relevant allele symbol.
Lethality
Allele
Sterility
Allele
Other Phenotypes
Allele
Phenotype manifest in
Allele
meiosis II & aster | female
meiosis II & spindle | female
meiotic cell cycle & spindle | male
meiotic metaphase II & spindle | female
meiotic telophase II & contractile ring | female
mitosis & nuclear chromosome
neuroblast & centrosome & larva
neuroblast & larval brain
neuroblast & larval brain | somatic clone
neuroblast & mitotic anaphase & larva
spermatocyte & midbody
spermatocyte & pericentriolar material
spermatocyte & spindle
spindle & neuroblast
Orthologs
Human Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Homo sapiens (Human) (50)
14 of 14
Yes
Yes
6 of 14
No
Yes
6 of 14
No
Yes
3 of 14
No
No
3 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
2  
1 of 14
No
No
2  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
2  
1 of 14
No
No
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
3  
1 of 14
No
No
2  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
2  
1 of 14
No
No
2  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1  
1 of 14
No
No
12  
1 of 14
No
No
2  
1 of 14
No
No
1  
1 of 14
No
No
2  
1 of 14
No
No
2  
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1  
1 of 14
No
No
1 of 14
No
No
1  
Model Organism Orthologs (via DIOPT v9.1)
Species\Gene Symbol
Score
Best Score
Best Reverse Score
Alignment
Complementation?
Transgene?
Rattus norvegicus (Norway rat) (26)
14 of 14
Yes
Yes
6 of 14
No
Yes
6 of 14
No
Yes
4 of 14
No
Yes
3 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Mus musculus (laboratory mouse) (25)
14 of 14
Yes
Yes
1  
6 of 14
No
Yes
6 of 14
No
Yes
4 of 14
No
Yes
3 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Xenopus tropicalis (Western clawed frog) (29)
11 of 13
Yes
Yes
4 of 13
No
Yes
4 of 13
No
Yes
4 of 13
No
Yes
3 of 13
No
Yes
2 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
Yes
1 of 13
No
Yes
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
Yes
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
Danio rerio (Zebrafish) (29)
13 of 14
Yes
Yes
6 of 14
No
Yes
6 of 14
No
Yes
6 of 14
No
Yes
3 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
Caenorhabditis elegans (Nematode, roundworm) (19)
13 of 14
Yes
Yes
12 of 14
No
Yes
10 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
No
1 of 14
No
Yes
1 of 14
No
No
1 of 14
No
No
Anopheles gambiae (African malaria mosquito) (14)
12 of 12
Yes
Yes
Arabidopsis thaliana (thale-cress) (41)
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
Yes
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
1 of 13
Yes
No
Saccharomyces cerevisiae (Brewer's yeast) (7)
13 of 13
Yes
Yes
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
1 of 13
No
No
Schizosaccharomyces pombe (Fission yeast) (6)
11 of 12
Yes
Yes
1 of 12
No
No
1 of 12
No
Yes
1 of 12
No
No
1 of 12
No
No
1 of 12
No
No
Escherichia coli (enterobacterium) (0)
Other Organism Orthologs (via OrthoDB)
Data provided directly from OrthoDB:polo. Refer to their site for version information.
Paralogs
Paralogs (via DIOPT v9.1)
Drosophila melanogaster (Fruit fly) (15)
5 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
1 of 13
Human Disease Associations
FlyBase Human Disease Model Reports
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Allele
Disease
Evidence
References
Potential Models Based on Orthology ( 0 )
Human Ortholog
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 6 )
Disease Associations of Human Orthologs (via DIOPT v9.1 and OMIM)
Note that ortholog calls supported by only 1 or 2 algorithms (DIOPT score < 3) are not shown.
Functional Complementation Data
Functional complementation data is computed by FlyBase using a combination of the orthology data obtained from DIOPT and OrthoDB and the allele-level genetic interaction data curated from the literature.
Interactions
Summary of Physical Interactions
Interaction Browsers

Please see the Physical Interaction reports below for full details
RNA-protein
Physical Interaction
Assay
References
protein-protein
Physical Interaction
Assay
References
Summary of Genetic Interactions
Interaction Browsers

Please look at the allele data for full details of the genetic interactions
Starting gene(s)
Interaction type
Interacting gene(s)
Reference
Starting gene(s)
Interaction type
Interacting gene(s)
Reference
External Data
Linkouts
BioGRID - A database of protein and genetic interactions.
DroID - A comprehensive database of gene and protein interactions.
MIST (genetic) - An integrated Molecular Interaction Database
MIST (protein-protein) - An integrated Molecular Interaction Database
Pathways
Signaling Pathways (FlyBase)
Metabolic Pathways
FlyBase
External Links
External Data
Class of Gene
Genomic Location and Detailed Mapping Data
Chromosome (arm)
3L
Recombination map
3-47
Cytogenetic map
Sequence location
FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
77B2-77B3
Limits computationally determined from genome sequence between P{lacW}l(3)L1243L1243&P{lacW}Mi-2j3D4 and P{PZ}eRF100103
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
77B1-77B2
(determined by in situ hybridisation)
77B-77B
(determined by in situ hybridisation) 77B3--7 (determined by in situ hybridisation)
77A-77A
(determined by in situ hybridisation)
77A3-77A3
(determined by in situ hybridisation)
Experimentally Determined Recombination Data
Location

3-46.8 +/- 0.1

3-46

Left of (cM)
Right of (cM)
Notes
Stocks and Reagents
Stocks (48)
Genomic Clones (15)
 

Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete

cDNA Clones (208)
 

Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.

cDNA clones, fully sequenced
BDGP DGC clones
Other clones
Drosophila Genomics Resource Center cDNA clones

For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.

cDNA Clones, End Sequenced (ESTs)
RNAi and Array Information
Linkouts
DRSC - Results frm RNAi screens
Antibody Information
Laboratory Generated Antibodies
Commercially Available Antibodies
 
Cell Line Information
Publicly Available Cell Lines
Other Stable Cell Lines
 
Other Comments

polo is required for efficient recruitment of pericentriolar material.

RNAi screen using dsRNA made from templates generated with primers directed against this gene causes decreased γ-tubulin staining at the spindle pole and detachment of the pole when assayed in S2 cells. This phenotype can be observed when the screen is performed with or without Cdc27 dsRNA.

polo acts as a tumor suppressor in the larval brain.

S2 cells treated with dsRNA generated against this gene show reduced phagocytosis of Candida albicans compared to untreated cells.

S2 cells transfected with dsRNA made from templates generated with primers directed against this gene show metaphase arrest.

When dsRNA constructs are made and transiently transfected into S2 cells in RNAi experiments, an increase in the proportion of G2/M phase cells, an increase, a decrease in cytokinetic index in mitotic index, a decrease in the ratio of cells in prometaphase and metaphase versus the total number of mitotic cells, a whole range of mitotic abnormalities, spindle abnormalities, centrosome abnormalities (no γ-tubulin at the poles) are seen.

dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.

RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a phenotype when assayed in Kc167 and S2R+ cells: cell morphology is aberrant and there is an increased frequency of microtubule-based mitotic spindles, indicative of a failure in mitosis.

Females homozygous for hypomorphic mutations in polo show defects both in the organisation of the central microtubule organising centre at meiosis II and in sperm aster formation.

polo is required at multiple stages during spermatogenesis.

polo protein kinase, in embryos, has a narrow peak of activity during late anaphase-telophase, separable from the peak of cdc2 activity.

A series of biochemical experiments demonstrate that polo is a Ser/Thr protein kinase which has to be phosphorylated to show kinase activity. Putative substrates (a β-tubulin and an 85kD microtubule-associated protein) can be specifically phosphorylated by polo.

Five genes essential for cell cycle progression, polo, mgr, asp, stg and gnu, are recombined onto a single chromosome, EMS mutations are isolated that fail to complement this chromosome. Genes encoding proteins that interact with the products of any of the five genes are isolated.

Mutations in polo lead to a variety of spindle defects including monopolar structures in larval brains and multipolar spindles in male meiosis. Embryos from mothers transheterozygous for mutations in polo and scant show bipolar spindles that have a centrosome only at one pole.

Defined by insertion of P{SUPor-P}.

polo gene product immunoprecipitated from single Drosophila embryos can phosphorylate casein in vitro, and the kinase activity peaks cyclically at late anaphase/telophase. This contrasts with the cycling of CycB-associated cdc2 histone H1 kinase, which is maximal upon entry into mitosis during the rapid syncitial mitoses. The polo product may regulate microtubule behaviour.

Immunocytological approach is used to address the behaviour of essential mitotic gene products in embryonic cell cycles.

polo has been cloned and sequences. It encodes a putative serine-threonine protein kinase.

Relationship to Other Genes
Source for database merge of

Source for merge of: polo l(3)01673

Source for merge of: polo l(3)77Aa

Source for merge of: polo l(3)S025604 l(3)S132408

Source for merge of: polo anon-WO0172774.3

Additional comments

Source for merge of polo anon-WO0172774.3 was sequence comparison ( date:051113 ).

Nomenclature History
Source for database identify of
Nomenclature comments
Etymology
Synonyms and Secondary IDs (18)
Reported As
Symbol Synonym
Polo
(Pimenta-Marques et al., 2024, Trujillo et al., 2024, Khalili et al., 2023, Loh et al., 2023, Warecki et al., 2023, Das and Arur, 2022, Wong et al., 2022, Alvarez-Rodrigo et al., 2021, Gillard et al., 2021, Wainman, 2021, Barbosa et al., 2020, Galander and Marston, 2020, Zheng et al., 2020, Bonner and Hawley, 2019, Hughes and Simmonds, 2019, Verma and Maresca, 2019, Carmena, 2018, Ramani et al., 2018, Tillery et al., 2018, Yao et al., 2018, Kachaner et al., 2017, Lattao et al., 2017, Meghini et al., 2016, Novak et al., 2016, Pimenta-Marques et al., 2016, Yadav et al., 2016, Eisman et al., 2015, Fu et al., 2015, Wan et al., 2015, Wang et al., 2015, Ahmad et al., 2014, Blanchard et al., 2014, Conduit et al., 2014, Sechi et al., 2014, Singh et al., 2014, Conde et al., 2013, Debruhl et al., 2013, Lerit and Rusan, 2013, Noatynska et al., 2013, Smith et al., 2013, Thomae et al., 2013, Wang et al., 2013, Carmena et al., 2012, Crest et al., 2012, Giansanti et al., 2012, Kelsom and Lu, 2012, Boke and Hagan, 2011, Szafer-Glusman et al., 2011, Akimana et al., 2010, Carvalho-Santos et al., 2010, Savoian and Glover, 2010, Torras-Llort et al., 2010, Yan, 2010, Blagden et al., 2009, Gilliland et al., 2009, McCleland et al., 2009, McCleland et al., 2009, Nie et al., 2009, Wang et al., 2009, Martins et al., 2008, McCleland and O'Farrell, 2008, Royou et al., 2008, Wen et al., 2008, Wen et al., 2008, D'Avino et al., 2007, Garcia et al., 2007, Goshima et al., 2007, Orr et al., 2007, Rusan and Peifer, 2007, Xiang et al., 2007, Liebl et al., 2006, Pines, 2006, Cytrynbaum et al., 2005, Coelho et al., 2003, Cornwell et al., 2002)
anon-WO0172774.3
l(3)S025604
l(3)S132408
polo
(Bischoff et al., 2025, Duan et al., 2025, Leclercq and Maurange, 2025, Najera et al., 2025, Xu et al., 2025, Rangone et al., 2024, Heigwer et al., 2023, Zhang et al., 2023, Frappaolo et al., 2022, Hannaford et al., 2022, Wong et al., 2022, Yang et al., 2022, Braun et al., 2021, Cattenoz et al., 2021, Csordás et al., 2021, Khan et al., 2021, Kump et al., 2021, Lebo et al., 2021, Ostalé et al., 2021, Cho et al., 2020, Gallaud et al., 2020, Izumi et al., 2020, Jeon et al., 2020, Khaminets et al., 2020, Landmann et al., 2020, Zhao et al., 2020, Archambault, 2019.11.16, Archambault, 2019.12.8, Blake-Hedges and Megraw, 2019, Deshpande et al., 2019, Liaw and Chiang, 2019, Oliveira et al., 2019, Rotelli et al., 2019, Sechi et al., 2019, Wang et al., 2019, Al-Ramahi et al., 2018, Hughes et al., 2018, Lee et al., 2018, Brose et al., 2017, Cheng et al., 2017, Hsu and Drummond-Barbosa, 2017, Transgenic RNAi Project members, 2017-, Ahmad et al., 2016, Das et al., 2016, Kong et al., 2016, Lee et al., 2016, Mao et al., 2016, Noble et al., 2016, Ramdas Nair et al., 2016, Varadarajan et al., 2016, Bouleau and Tricoire, 2015, Chittaranjan et al., 2015, Di Cara et al., 2015, Eisman et al., 2015, Fischer et al., 2015, Kanoh et al., 2015, Peng et al., 2015, Sanchez-Alvarez et al., 2015, Ahmad et al., 2014, Carmena et al., 2014, Hughes et al., 2014, Kitazawa et al., 2014, Nakayama et al., 2014, Riparbelli et al., 2014, Savoian and Glover, 2014, Sopko et al., 2014, Taniguchi et al., 2014, Tipping and Perrimon, 2014, Vinayagam et al., 2014, Bonner et al., 2013, Kwon et al., 2013, Moshkin et al., 2013, Noatynska et al., 2013, Schertel et al., 2013, Whitfield et al., 2013, Yin et al., 2013, Zhan et al., 2013, Ahmad et al., 2012, Azad et al., 2012, Giansanti et al., 2012, Habermann et al., 2012, Japanese National Institute of Genetics, 2012.5.21, Joyce et al., 2012, Korenjak et al., 2012, Lesch and Page, 2012, McKee et al., 2012, Miller et al., 2012, Pek et al., 2012, Tao et al., 2012, Michaut et al., 2011, Ouyang et al., 2011, Pinto et al., 2011, Rangone et al., 2011, Reis et al., 2011, Szafer-Glusman et al., 2011, Wang et al., 2011, Chang et al., 2010, Ebrahimi et al., 2010, Januschke and Gonzalez, 2010, Müller et al., 2010, Royou et al., 2010, Anderson et al., 2009, Christensen et al., 2009.2.28, Gilliland et al., 2009, Liu et al., 2009, Venken et al., 2009, Zhang et al., 2009, Archambault et al., 2008, Bakal et al., 2008, Castellanos et al., 2008, Chia et al., 2008, Christensen et al., 2008.4.15, Dobbelaere et al., 2008, Godinho and Tavares, 2008, Mattila et al., 2008, McClure and Schubiger, 2008, Schuldiner et al., 2008, Somma et al., 2008, Von Stetina et al., 2008, Wittkopp et al., 2008, Basto et al., 2007, Brittle et al., 2007, Buszczak et al., 2007, Georlette et al., 2007, Gilliland et al., 2007, Gilliland et al., 2007, Goshima et al., 2007, Jiang et al., 2007, Kaplow et al., 2007, Magalhaes et al., 2007, Slack et al., 2007, Stuart et al., 2007, Wang et al., 2007, Williams et al., 2007, Xiang et al., 2007, Xing et al., 2007, Yi et al., 2007, Cesario et al., 2006, Delcros et al., 2006, Foglietti et al., 2006, Mirouse et al., 2006, Mukai et al., 2006, Pearson et al., 2006, Rivera and Losada, 2006, Slack et al., 2006, Stroschein-Stevenson et al., 2006, Clarke et al., 2005, Gatt et al., 2005, Jang et al., 2005, Lake and Hawley, 2005, Laviolette et al., 2005, Liebl and Featherstone, 2005, Loop et al., 2004, Stanyon et al., 2004, Blagden and Glover, 2003, Carpenter, 2003, Leismann and Lehner, 2003)
Secondary FlyBase IDs
  • FBgn0010758
  • FBgn0016019
  • FBgn0027987
  • FBgn0028177
  • FBgn0046400
Datasets (0)
Study focus (0)
Experimental Role
Project
Project Type
Title
Study result (0)
Result
Result Type
Title
External Crossreferences and Linkouts ( 62 )
Sequence Crossreferences
NCBI Gene - Gene integrates information from a wide range of species. A record may include nomenclature, Reference Sequences (RefSeqs), maps, pathways, variations, phenotypes, and links to genome-, phenotype-, and locus-specific resources worldwide.
GenBank Nucleotide - A collection of sequences from several sources, including GenBank, RefSeq, TPA, and PDB.
GenBank Protein - A collection of sequences from several sources, including translations from annotated coding regions in GenBank, RefSeq and TPA, as well as records from SwissProt, PIR, PRF, and PDB.
RefSeq - A comprehensive, integrated, non-redundant, well-annotated set of reference sequences including genomic, transcript, and protein.
UniProt/GCRP - The gene-centric reference proteome (GCRP) provides a 1:1 mapping between genes and UniProt accessions in which a single 'canonical' isoform represents the product(s) of each protein-coding gene.
UniProt/Swiss-Prot - Manually annotated and reviewed records of protein sequence and functional information
Other crossreferences
AlphaFold DB - AlphaFold provides open access to protein structure predictions for the human proteome and other key proteins of interest, to accelerate scientific research.
DRscDB - A single-cell RNA-seq resource for data mining and data comparison across species
EMBL-EBI Single Cell Expression Atlas - Single cell expression across species
FlyAtlas2 - A Drosophila melanogaster expression atlas with RNA-Seq, miRNA-Seq and sex-specific data
FlyMine - An integrated database for Drosophila genomics
KEGG Genes - Molecular building blocks of life in the genomic space.
MARRVEL_MODEL - MARRVEL (model organism gene)
Linkouts
BioGRID - A database of protein and genetic interactions.
Drosophila Genomics Resource Center - Drosophila Genomics Resource Center (DGRC) cDNA clones
DroID - A comprehensive database of gene and protein interactions.
DRSC - Results frm RNAi screens
Eukaryotic Promoter Database - A collection of databases of experimentally validated promoters for selected model organisms.
FlyAtlas - Adult expression by tissue, using Affymetrix Dros2 array
FlyCyc Genes - Genes from a BioCyc PGDB for Dmel
Fly-FISH - A database of Drosophila embryo and larvae mRNA localization patterns
Flygut - An atlas of the Drosophila adult midgut
FlyMet - A comprehensive tissue-specific metabolomics resource for Drosophila.
iBeetle-Base - RNAi phenotypes in the red flour beetle (Tribolium castaneum)
Interactive Fly - A cyberspace guide to Drosophila development and metazoan evolution
KEGG Pathways - A collection of manually drawn pathway maps representing knowledge of molecular interaction, reaction and relation networks.
MIST (genetic) - An integrated Molecular Interaction Database
MIST (protein-protein) - An integrated Molecular Interaction Database
SignaLink - A signaling pathway resource with multi-layered regulatory networks.
References (441)