Q9W2E7 · RAE1_DROME
- ProteinProtein Rae1
- GeneRae1
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids346 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Function
function
Probable component of the nuclear pore complex (NPC) which regulates the nuclear export of specific mRNAs and promotes cell cycle progression during mitosis and male meiosis (PubMed:14729268, PubMed:23788425, PubMed:27494403).
Acts with Nup98-96 to promote the nuclear export of specific mRNAs such as Moe, however it does not appear to be required for general nuclear mRNA transport (PubMed:14729268, PubMed:28554770).
Essential mitotic and male meiotic cell cycle regulator with roles in many aspects of the cell cycle including chromatin organization and condensation, spindle assembly, chromosome segregation, and maintaining nuclear structure (PubMed:14729268, PubMed:23788425, PubMed:27494403).
During male meiosis it is required for completion of meiosis I, as well as accurate cytokinesis of the secondary spermatocytes, and postmeiotic differentiation of spermatids (PubMed:23788425).
Acts as a downstream regulatory target of the Hippo/SWH (Sav/Wts/Hpo) signaling pathway to promote mitotic cell cycle progression and proliferation during wing and eye development, and thereby plays a key role in integrating the regulation of proliferation with organ size control (PubMed:14729268, PubMed:27494403).
When the Hippo/SWH signaling pathway is inactive, Rae1 acts independently of yki to increase organ size by promoting mitotic S-phase entry and increase cellular proliferation (PubMed:27494403).
When the Hippo/SWH signaling pathway is active it inhibits the activity of Rae1 in a Wts-dependent manner to restrict organ growth (PubMed:27494403).
However, Rae1 is also able to negatively regulate the levels and activity of yki likely by activating the core kinases of the Hippo/SWH signaling pathway hpo and Wts and increasing the protein levels of hpo, Mer and Wts; it is therefore likely that it functions as part of a negative feedback loop with the Hippo/SWH signaling pathway to regulate pathway homeostasis and prevent organ overgrowth (PubMed:27494403).
Promotes mitotic cell cycle progression, at least in part, by increasing the accumulation of mitotic cyclins such as CycB, possibly by directly up-regulating cyclin transcripts or by inhibiting the anaphase promoting complex/cyclosome (APC/C) activator fzy (PubMed:27494403).
Also required in presynaptic, postmitotic motor neurons to restrain synaptic terminal growth (PubMed:21874015).
Promotes the expression and stability of the an E3 ubiquitin ligase of hiw, and is likely to function in the regulation of synaptic growth by binding to hiw and protecting it from autophagy-mediated degradation (PubMed:21874015).
Acts with Nup98-96 to promote the nuclear export of specific mRNAs such as Moe, however it does not appear to be required for general nuclear mRNA transport (PubMed:14729268, PubMed:28554770).
Essential mitotic and male meiotic cell cycle regulator with roles in many aspects of the cell cycle including chromatin organization and condensation, spindle assembly, chromosome segregation, and maintaining nuclear structure (PubMed:14729268, PubMed:23788425, PubMed:27494403).
During male meiosis it is required for completion of meiosis I, as well as accurate cytokinesis of the secondary spermatocytes, and postmeiotic differentiation of spermatids (PubMed:23788425).
Acts as a downstream regulatory target of the Hippo/SWH (Sav/Wts/Hpo) signaling pathway to promote mitotic cell cycle progression and proliferation during wing and eye development, and thereby plays a key role in integrating the regulation of proliferation with organ size control (PubMed:14729268, PubMed:27494403).
When the Hippo/SWH signaling pathway is inactive, Rae1 acts independently of yki to increase organ size by promoting mitotic S-phase entry and increase cellular proliferation (PubMed:27494403).
When the Hippo/SWH signaling pathway is active it inhibits the activity of Rae1 in a Wts-dependent manner to restrict organ growth (PubMed:27494403).
However, Rae1 is also able to negatively regulate the levels and activity of yki likely by activating the core kinases of the Hippo/SWH signaling pathway hpo and Wts and increasing the protein levels of hpo, Mer and Wts; it is therefore likely that it functions as part of a negative feedback loop with the Hippo/SWH signaling pathway to regulate pathway homeostasis and prevent organ overgrowth (PubMed:27494403).
Promotes mitotic cell cycle progression, at least in part, by increasing the accumulation of mitotic cyclins such as CycB, possibly by directly up-regulating cyclin transcripts or by inhibiting the anaphase promoting complex/cyclosome (APC/C) activator fzy (PubMed:27494403).
Also required in presynaptic, postmitotic motor neurons to restrain synaptic terminal growth (PubMed:21874015).
Promotes the expression and stability of the an E3 ubiquitin ligase of hiw, and is likely to function in the regulation of synaptic growth by binding to hiw and protecting it from autophagy-mediated degradation (PubMed:21874015).
GO annotations
Keywords
- Biological process
Enzyme and pathway databases
Names & Taxonomy
Protein names
- Recommended nameProtein Rae1
Gene names
Organism names
- Strain
- Taxonomic lineageEukaryota > Metazoa > Ecdysozoa > Arthropoda > Hexapoda > Insecta > Pterygota > Neoptera > Endopterygota > Diptera > Brachycera > Muscomorpha > Ephydroidea > Drosophilidae > Drosophila > Sophophora
Accessions
- Primary accessionQ9W2E7
- Secondary accessions
Proteomes
Organism-specific databases
Subcellular Location
UniProt Annotation
GO Annotation
Note: Dynamic pattern of localization during the spermatocyte cell cycle. Perinuclear in young primary spermatocytes. In late meiotic prophase spermatocytes, localizes to the nucleus where it co-localizes with three major chromatin clumps, and is also associated with puncta in the cytoplasm. In anaphase I and telophase I, occurs at segregating chromatin and mitochondria localized between the two daughter nuclei. In post-meiotic onion stage spermatids, mainly associates with the Nebenkern (a mitochondrial formation in the sperm) but is not detected at the nucleus.
Keywords
- Cellular component
Phenotypes & Variants
Disruption phenotype
Larval lethal (PubMed:27494403).
Larvae die at the third-instar stage (PubMed:27494403).
RNAi-mediated knockdown in the testes results in male sterility likely due to defects in primary spermatocyte nuclear integrity, meiotic chromosome condensation, segregation, and spindle morphology (PubMed:23788425).
These defects lead to a failure to complete meiosis but several aspects of spermatid differentiation can still proceed, including axoneme formation and elongation (PubMed:23788425).
RNAi-mediated knockdown in the developing wing or in the proliferating cells of the developing eye, reduces their organ size (PubMed:27494403).
RNAi-mediated knockdown in larval neuroblasts results in chromatin undercondensation in metaphase chromosomes (PubMed:23788425).
RNAi-mediated knockdown in differentiating eye cells does not result in an obvious phenotype (PubMed:27494403).
Larvae die at the third-instar stage (PubMed:27494403).
RNAi-mediated knockdown in the testes results in male sterility likely due to defects in primary spermatocyte nuclear integrity, meiotic chromosome condensation, segregation, and spindle morphology (PubMed:23788425).
These defects lead to a failure to complete meiosis but several aspects of spermatid differentiation can still proceed, including axoneme formation and elongation (PubMed:23788425).
RNAi-mediated knockdown in the developing wing or in the proliferating cells of the developing eye, reduces their organ size (PubMed:27494403).
RNAi-mediated knockdown in larval neuroblasts results in chromatin undercondensation in metaphase chromosomes (PubMed:23788425).
RNAi-mediated knockdown in differentiating eye cells does not result in an obvious phenotype (PubMed:27494403).
Features
Showing features for mutagenesis.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Mutagenesis | 129 | Male sterility. Spermatocytes display various defects during early meiotic stages, post-meiotic stages and late spermatogenesis. Defects in early meiotic stages result in karyokinesis and cytokinesis abnormailities and a failure to complete meiosis I. Differentiation arrest prior to spermatid individualization results in seminal vesicles lacking mature sperm. | ||||
Sequence: G → D |
PTM/Processing
Features
Showing features for chain.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Chain | PRO_0000450094 | 1-346 | Protein Rae1 | |||
Sequence: MFGATQSTNRMNDFEVASPPDDSVSALEFSPSTVQKNFLVAGSWDSTVRCWEVEQNGATVPKSMKTMGGPVLDVCWSDDGSKVFVASCDKQVKLWDLASDQVMQVAAHDGPVKTCHMVKGPTYTCLMTGSWDKTLKFWDTRSPNPMMTINLPERCYCADVEYPMAVVGTANRGLIIYSLQNSPTEYKRQESPLKYQHRAISIFRDKKKEPTGCALGSIEGRVAIQYVNPGNPKDNFTFKCHRTTGTSGYQDIYAVNDIAFHPVHGTLVTVGSDGTFSFWDKDARTKLKSSETMDQSITKCGFNANGQIFAYAVGYDWSKGHEYFNPAKKPQIFLRSCYDELKPRIN |
Proteomic databases
Expression
Tissue specificity
Head (at protein level).
Developmental stage
Larval brain (at protein level).
Gene expression databases
Structure
Family & Domains
Features
Showing features for repeat.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Repeat | 17-61 | WD 1 | ||||
Sequence: ASPPDDSVSALEFSPSTVQKNFLVAGSWDSTVRCWEVEQNGATVP | ||||||
Repeat | 64-105 | WD 2 | ||||
Sequence: MKTMGGPVLDVCWSDDGSKVFVASCDKQVKLWDLASDQVMQV | ||||||
Repeat | 126-148 | WD 3 | ||||
Sequence: LMTGSWDKTLKFWDTRSPNPMMT | ||||||
Repeat | 255-289 | WD 4 | ||||
Sequence: VNDIAFHPVHGTLVTVGSDGTFSFWDKDARTKLKS |
Sequence similarities
Belongs to the WD repeat rae1 family.
Keywords
- Domain
Phylogenomic databases
Family and domain databases
Sequence
- Sequence statusComplete
- Length346
- Mass (Da)38,618
- Last updated2000-05-01 v1
- Checksum17E4650B83E692A2
Sequence caution
Keywords
- Technical term
Sequence databases
Nucleotide Sequence | Protein Sequence | Molecule Type | Status | |
---|---|---|---|---|
AE013599 EMBL· GenBank· DDBJ | AAF46745.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AY118568 EMBL· GenBank· DDBJ | AAM49937.2 EMBL· GenBank· DDBJ | mRNA | Different initiation |