Mtor, Bx34, Tpr, l(2)k03905
signaling protein that promotes the recruitment of Mad2 and Mps1 to unattached kinetochores, mediating normal mitotic duration and spindle assembly checkpoint response
Please see the JBrowse view of Dmel\Mgtor for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.45
8 (northern blot)
2346 (aa); 260 (kD observed); 262 (kD predicted)
Part of the nuclear pore complex (NPC) (PubMed:12027452, PubMed:22855526, PubMed:9152019). Associates with male-specific lethal (MSL) histone acetyltransferase complex (PubMed:16543150). Interacts with Mad2; the interaction is required for efficient recruitment of Mad2 to unattached kinetochore and occurs in a microtubule-independent manner (PubMed:19273613). Interacts with Mad1 (N-terminus) (PubMed:31913420). Interacts with Chro, east and Asator; the interaction is part of a macromolecular complex forming the spindle matrix during mitosis (PubMed:15356261, PubMed:15962301, PubMed:19890914). Interacts with Nup98 (PubMed:28366641). In males, interacts with histone acetyltransferase mof (PubMed:34133927).
Mps1-mediated phosphorylation disrupts interaction with Mad1 during mitosis.
The N-terminal coiled-coil domain is required for both nuclear pore complex (NPC) and spindle matrix localization.
The C-terminal domain is required for interchromosomal localization during interphase (PubMed:15356261). The C-terminal domain is sufficient for localization to the nuclear lamina as well as for spindle localization (PubMed:15356261).
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Mgtor using the Feature Mapper tool.
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).
Mgtor protein localizes to the nuclear interior in embryonic, larval and adult cell types studied.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Mgtor in JBrowse2-65
2-66.0
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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.
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.
polyclonal
dsRNA made from templates generated with primers directed against this gene and injected into S2 cells causes a reduction in the number of cells undergoing mitosis.
Homozygous embryos die before hatching and have spindle abnormalities and chromosome segregation defects.
Area matching Drosophila Tpr homologue gene, Acc. No. U91980.
Isolated from a 0-16 hour embryo cDNA expression library, using monoclonal antibodies Mtor and Bx93 as probes.
Mtor has been cloned and sequenced, and its expression pattern and localisation within the cell has been determined.
Mtor gene product localises to the nuclear periphery in interphase, remains concentrated in the chromosomal region during metaphase and early anaphase, and isolates biochemically in the nuclear pore complex-lamina fraction (FBrf0048434).
Source for merge of: Mtor l(2)k03905
Source for identity of: Tpr Megator
Source for identity of: Mgtor Mtor
Changed gene symbol 'Mtor' to 'Mgtor' to minimise confusion with the 'Tor' gene, which is the ortholog of vertebrate MTOR and is often referred to as such in flies.