Information report for AT3G13170
Gene Details
|
|
Functional Descriptions
- PO:0000037 — shoot axis apex — ápice del epiblasto (epiblastema) (Spanish, exact), シュート頂、茎頂 (Japanese, exact)
- PO:0009009 — plant embryo — embrión (Spanish, exact), 植物胚 (Japanese, exact), germ (related), embryo (broad)
- PO:0009046 — flower — flor (Spanish, exact), 花 (Japanese, exact), floret (related), Asteraceae floret (narrow), basal flower (narrow), double flower (narrow), hermaphrodite flower (narrow), monoclinous flower (narrow), perfect flower (narrow)
- PO:0009052 — inflorescence flower pedicel — 小花柄 (Japanese, related), pedicelo (Spanish, broad)
- atcom1-1 atspo11-1-1 — DNA fragmentation was undetectable in most cells.
- atspo11-1-1 — 11% of mutant pollen grains germinated compared to 97% for wild type.
- atspo11-1-1 — Mutant produced a large proportion of dead pollen grains compared to wild type.
- atspo11-1-1 — Only 3% of the ovules in the mutant showed differentiated female gametophytes. 74% of the fully developed ovules had no embryo sac.
- atspo11-1-1 — Overall morphology similar to that of wild type exception made of the seed production.
- atspo11-1-1 — The mutant exhibits a substantial reduction in recombination such that the chiasma frequency at metaphase I was &
- atspo11-1-2 — 11% of mutant pollen grains germinated compared to 97% for wild type.
- atspo11-1-2 — Mutant produced a large proportion of dead pollen grains compared to wild type.
- atspo11-1-2 — Only 3% of the ovules in the mutant showed differentiated female gametophytes. 74% of the fully developed ovules had no embryo sac.
- atspo11-1-2 — Overall morphology similar to that of wild type exception made of the seed production.
- atspo11-1-3 — A 2-h pulse of cisplatin at increasing concentrations was found to restore bivalent formation in Atspo11-1-3 meiocytes.
- atspo11-1-3 — The reduction in seed-set in the Atspo11-1-3 allele is more severe than in Atspo11-1-1.
- atspo11-1-3 — Total lack of chiasmata.
- spo11-1-3 spo-2-3 — The first meiotic division of pollen mother cells because the homologs neither pair nor form SCs due to the lack of initial DSB formation
Functional Keywords
Literature and News
- ASY1 mediates AtDMC1-dependent interhomolog recombination during meiosis in Arabidopsis. DOI: 10.1101/gad.439007 ; PMID: 17785529
- The catalytically active tyrosine residues of both SPO11-1 and SPO11-2 are required for meiotic double-strand break induction in Arabidopsis. DOI: 10.1105/tpc.107.054817 ; PMID: 17965269
- A high throughput genetic screen identifies new early meiotic recombination functions in Arabidopsis thaliana. DOI: 10.1371/journal.pgen.1000654 ; PMID: 19763177
- A DNA-binding surface of SPO11-1, an Arabidopsis SPO11 orthologue required for normal meiosis. DOI: 10.1111/j.1742-4658.2010.07651.x ; PMID: 20423461
- The cyclin-A CYCA1;2/TAM is required for the meiosis I to meiosis II transition and cooperates with OSD1 for the prophase to first meiotic division transition. DOI: 10.1371/journal.pgen.1000989 ; PMID: 20585549
- A DNA topoisomerase VI-like complex initiates meiotic recombination. DOI: 10.1126/science.aad5196 ; PMID: 26917763
- MTOPVIB interacts with AtPRD1 and plays important roles in formation of meiotic DNA double-strand breaks in Arabidopsis. DOI: 10.1038/s41598-017-10270-9 ; PMID: 28855712
- FIGL1 and its novel partner FLIP form a conserved complex that regulates homologous recombination. DOI: 10.1371/journal.pgen.1007317 ; PMID: 29608566
- Meiocyte-Specific and AtSPO11-1-Dependent Small RNAs and Their Association with Meiotic Gene Expression and Recombination. DOI: 10.1105/tpc.18.00511 ; PMID: 30674694
- Both male and female gametogenesis require a fully functional protein S-acyl transferase 21 in Arabidopsis thaliana. DOI: 10.1111/tpj.14475 ; PMID: 31369173
- ATM controls meiotic DNA double-strand break formation and recombination and affects synaptonemal complex organization in plants. DOI: 10.1093/plcell/koab045 ; PMID: 33659989
- Heat stress interferes with formation of double-strand breaks and homolog synapsis. DOI: 10.1093/plphys/kiab012 ; PMID: 33793950
- Defects in meiotic chromosome segregation lead to unreduced male gametes in Arabidopsis SMC5/6 complex mutants. DOI: 10.1093/plcell/koab178 ; PMID: 34240187
- Heterologous Complementation of SPO11-1 and -2 Depends on the Splicing Pattern. DOI: 10.3390/ijms22179346 ; PMID: 34502253
- Coexpression of MEIOTIC-TOPOISOMERASE VIB-dCas9 with guide RNAs specific to a recombination hotspot is insufficient to increase crossover frequency in Arabidopsis. DOI: 10.1093/g3journal/jkac105 ; PMID: 35485960
- Differentiated function and localisation of SPO11-1 and PRD3 on the chromosome axis during meiotic DSB formation in Arabidopsis thaliana. DOI: 10.1371/journal.pgen.1010298 ; PMID: 35857772
- Tracing the evolution of the plant meiotic molecular machinery. DOI: 10.1007/s00497-022-00456-1 ; PMID: 36646915
- Arabidopsis SPO11-2 functions with SPO11-1 in meiotic recombination. DOI: 10.1111/j.1365-313X.2006.02867.x ; PMID: 17018031
- ASY1 mediates AtDMC1-dependent interhomolog recombination during meiosis in Arabidopsis. DOI: 10.1101/gad.439007 ; PMID: 17785529
- The catalytically active tyrosine residues of both SPO11-1 and SPO11-2 are required for meiotic double-strand break induction in Arabidopsis. DOI: 10.1105/tpc.107.054817 ; PMID: 17965269
- A DNA topoisomerase VI-like complex initiates meiotic recombination. DOI: 10.1126/science.aad5196 ; PMID: 26917763
Gene Resources
- UniProt: A0A1I9LQV8
- EMBL: CP002686
- AlphaFoldDB: A0A1I9LQV8
- EnsemblPlants: AT3G13170.2, AT3G13170.3
- Gramene: AT3G13170.2, AT3G13170.3
- ExpressionAtlas: AT3G13170
- InterPro: IPR002815, IPR013049, IPR034136
- PANTHER: PTHR10848, PTHR10848:SF3
- SUPFAM: SSF56726
- Gene3D: 1.10.10.10, 3.40.1360.10
- SWISS-MODEL: A0A1I9LQV8
- Conserved Domain Database: cd00223
Homologs
- Oryza sativa OsSPO11-1;OsTOP6A1, OsTOP6A3, OsSpo11-4;OsSPO11D, TOP6A2;OsTOP6A2, OsSpo11-5
- Triticum aestivum TaSPO11-1-5D, TaSPO11-1-5B, TaSPO11-1-5A, TaSPO11-2-7A, TaSPO11-2-7B, TaSPO11-2-7D
Sequences
cDNA Sequence
- >AT3G13170.3
ATGGAGGGAAAATTCGCTATTTCAGAATCGACTAATTTGCTTCAAAGGATCAAAGATTTTACTCAATCGGTCGTTGTAGATCTGGCTGAAGGAAGATCTCCAAAAATTTCCATCAATCAATTCAGGAACTATTGCATGAATCCAGAAGCTGATTGCTTATGCAGCTCTGATAAACCAAAGGGTCAGGAAATTTTCACTCTTAAGAAGGAACCACAAACCTACAGAATCGATATGTTGCTAAGAGTATTGTTGATAGTCCAACAACTTCTGCAAGAAAATAGACATGCTTCGAAAAGAGATATCTACTACATGCATCCATCAGCTTTCAAAGCACAATCCATTGTGGACCGTGCAATTGGTGATATATGCATTCTTTTTCAGTGTAGTCGGTACAACTTGAATGTGGTTTCTGTTGGAAACGGGTTGGTGATGGGTTGGTTAAAATTTAGGGAAGCTGGAAGGAAATTTGATTGTTTAAACAGCTTGAACACTGCATATCCCGTTCCTGTTCTTGTAGAGGAAGTCGAAGATATTGTTAGCTTAGCTGAGTACATACTGGTTGTGGAAAAAGAAACAGTATTCCAGCGTTTAGCAAATGACATGTTTTGCAAGACGAACCGCTGCATTGTTATCACAGGAAGAGGATATCCAGATGTCTCAACAAGAAGGTTCTTGCGACTCCTGATGGAGAAGTTGCATCTACCTGTGCATTGTCTAGTCGACTGTGATCCATATGGCTTTGAGATCCTAGCCACATACCGTTTTGGCTCCATGGTTAGATTCTGTTACAAAATATAGATGACTGAACTCGGAAAATTTCACCGCTTGCATTGTTTTTGTTGATAGTGATAATGTGATATGGCAC - >AT3G13170.2
ATGGAGGGAAAATTCGCTATTTCAGAATCGACTAATTTGCTTCAAAGGATCAAAGATTTTACTCAATCGGTCGTTGTAGATCTGGCTGAAGGAAGATCTCCAAAAATTTCCATCAATCAATTCAGGAACTATTGCATGAATCCAGAAGCTGATTGCTTATGCAGCTCTGATAAACCAAAGGGTCAGGAAATTTTCACTCTTAAGAAGGAACCACAAACCTACAGAATCGATATGTTGCTAAGAGTATTGTTGATAGTCCAACAACTTCTGCAAGAAAATAGACATGCTTCGAAAAGAGATATCTACTACATGCATCCATCAGCTTTCAAAGCACAATCCATTGTGGACCGTGCAATTGGTGATATATGCATTCTTTTTCAGTGTAGTCGGTACAACTTGAATGTGGTTTCTGTTGGAAACGGGTTGGTGATGGGTTGGTTAAAATTTAGGGAAGCTGGAAGGAAATTTGATTGTTTAAACAGCTTGAACACTGCATATCCCGTTCCTGTTCTTGTAGAGGAAGTCGAAGATATTGTTAGCTTAGCTGAGTACATACTGGTTGTGGAAAAAGAAACAGTATTCCAGCGTTTAGCAAATGACATGTTTTGCAAGACGAACCGCTGCATTGTTATCACAGGAAGAGGATATCCAGATGTCTCAACAAGAAGGTTCTTGCGACTCCTGATGGAGAAGTTGCATCTACCTGTGCATTGTCTAGTCGACTGTGATCCATATGGCTTTGAGATCCTAGCCACATACCGTTTTGGCTCCATGGTTAGATTCTGTTACAAAATATAGATGACTGAACTCGGAAAATTTCACCGCTTGCATTGTTTTTGTTGATAGTGATAATGTGATATGGCAC - >AT3G13170.1
ATGGAGGGAAAATTCGCTATTTCAGAATCGACTAATTTGCTTCAAAGGATCAAAGATTTTACTCAATCGGTCGTTGTAGATCTGGCTGAAGGAAGATCTCCAAAAATTTCCATCAATCAATTCAGGAACTATTGCATGAATCCAGAAGCTGATTGCTTATGCAGCTCTGATAAACCAAAGGGTCAGGAAATTTTCACTCTTAAGAAGGAACCACAAACCTACAGAATCGATATGTTGCTAAGAGTATTGTTGATAGTCCAACAACTTCTGCAAGAAAATAGACATGCTTCGAAAAGAGATATCTACTACATGCATCCATCAGCTTTCAAAGCACAATCCATTGTGGACCGTGCAATTGGTGATATATGCATTCTTTTTCAGTGTAGTCGGTACAACTTGAATGTGGTTTCTGTTGGAAACGGGTTGGTGATGGGTTGGTTAAAATTTAGGGAAGCTGGAAGGAAATTTGATTGTTTAAACAGCTTGAACACTGCATATCCCGTTCCTGTTCTTGTAGAGGAAGTCGAAGATATTGTTAGCTTAGCTGAGTACATACTGGTTGTGGAAAAAGAAACAGTATTCCAGCGTTTAGCAAATGACATGTTTTGCAAGACGAACCGCTGCATTGTTATCACAGGAAGAGGATATCCAGATGTCTCAACAAGAAGGTTCTTGCGACTCCTGATGGAGAAGTTGCATCTACCTGTGCATTGTCTAGTCGACTGTGATCCATATGGCTTTGAGATCCTAGCCACATACCGTTTTGGCTCCATGGTTAGATTCTGTTACAAAATATAGATGACTGAACTCGGAAAATTTCACCGCTTGCATTGTTTTTGTTGATAGTGATAATGTGATATGGCAC
CDS Sequence
- >AT3G13170.3
ATGGAGGGAAAATTCGCTATTTCAGAATCGACTAATTTGCTTCAAAGGATCAAAGATTTTACTCAATCGGTCGTTGTAGATCTGGCTGAAGGAAGATCTCCAAAAATTTCCATCAATCAATTCAGGAACTATTGCATGAATCCAGAAGCTGATTGCTTATGCAGCTCTGATAAACCAAAGGGTCAGGAAATTTTCACTCTTAAGAAGGAACCACAAACCTACAGAATCGATATGTTGCTAAGAGTATTGTTGATAGTCCAACAACTTCTGCAAGAAAATAGACATGCTTCGAAAAGAGATATCTACTACATGCATCCATCAGCTTTCAAAGCACAATCCATTGTGGACCGTGCAATTGGTGATATATGCATTCTTTTTCAGTGTAGTCGGTACAACTTGAATGTGGTTTCTGTTGGAAACGGGTTGGTGATGGGTTGGTTAAAATTTAGGGAAGCTGGAAGGAAATTTGATTGTTTAAACAGCTTGAACACTGCATATCCCGTTCCTGTTCTTGTAGAGGAAGTCGAAGATATTGTTAGCTTAGCTGAGTACATACTGGTTGTGGAAAAAGAAACAGTATTCCAGCGTTTAGCAAATGACATGTTTTGCAAGACGAACCGCTGCATTGTTATCACAGGAAGAGGATATCCAGATGTCTCAACAAGAAGGTTCTTGCGACTCCTGATGGAGAAGTTGCATCTACCTGTGCATTGTCTAGTCGACTGTGATCCATATGGCTTTGAGATCCTAGCCACATACCGTTTTGGCTCCATGGTTAGATTCTGTTACAAAATATAG - >AT3G13170.2
ATGGAGGGAAAATTCGCTATTTCAGAATCGACTAATTTGCTTCAAAGGATCAAAGATTTTACTCAATCGGTCGTTGTAGATCTGGCTGAAGGAAGATCTCCAAAAATTTCCATCAATCAATTCAGGAACTATTGCATGAATCCAGAAGCTGATTGCTTATGCAGCTCTGATAAACCAAAGGGTCAGGAAATTTTCACTCTTAAGAAGGAACCACAAACCTACAGAATCGATATGTTGCTAAGAGTATTGTTGATAGTCCAACAACTTCTGCAAGAAAATAGACATGCTTCGAAAAGAGATATCTACTACATGCATCCATCAGCTTTCAAAGCACAATCCATTGTGGACCGTGCAATTGGTGATATATGCATTCTTTTTCAGTGTAGTCGGTACAACTTGAATGTGGTTTCTGTTGGAAACGGGTTGGTGATGGGTTGGTTAAAATTTAGGGAAGCTGGAAGGAAATTTGATTGTTTAAACAGCTTGAACACTGCATATCCCGTTCCTGTTCTTGTAGAGGAAGTCGAAGATATTGTTAGCTTAGCTGAGTACATACTGGTTGTGGAAAAAGAAACAGTATTCCAGCGTTTAGCAAATGACATGTTTTGCAAGACGAACCGCTGCATTGTTATCACAGGAAGAGGATATCCAGATGTCTCAACAAGAAGGTTCTTGCGACTCCTGATGGAGAAGTTGCATCTACCTGTGCATTGTCTAGTCGACTGTGATCCATATGGCTTTGAGATCCTAGCCACATACCGTTTTGGCTCCATGGTTAGATTCTGTTACAAAATATAG - >AT3G13170.1
ATGGAGGGAAAATTCGCTATTTCAGAATCGACTAATTTGCTTCAAAGGATCAAAGATTTTACTCAATCGGTCGTTGTAGATCTGGCTGAAGGAAGATCTCCAAAAATTTCCATCAATCAATTCAGGAACTATTGCATGAATCCAGAAGCTGATTGCTTATGCAGCTCTGATAAACCAAAGGGTCAGGAAATTTTCACTCTTAAGAAGGAACCACAAACCTACAGAATCGATATGTTGCTAAGAGTATTGTTGATAGTCCAACAACTTCTGCAAGAAAATAGACATGCTTCGAAAAGAGATATCTACTACATGCATCCATCAGCTTTCAAAGCACAATCCATTGTGGACCGTGCAATTGGTGATATATGCATTCTTTTTCAGTGTAGTCGGTACAACTTGAATGTGGTTTCTGTTGGAAACGGGTTGGTGATGGGTTGGTTAAAATTTAGGGAAGCTGGAAGGAAATTTGATTGTTTAAACAGCTTGAACACTGCATATCCCGTTCCTGTTCTTGTAGAGGAAGTCGAAGATATTGTTAGCTTAGCTGAGTACATACTGGTTGTGGAAAAAGAAACAGTATTCCAGCGTTTAGCAAATGACATGTTTTGCAAGACGAACCGCTGCATTGTTATCACAGGAAGAGGATATCCAGATGTCTCAACAAGAAGGTTCTTGCGACTCCTGATGGAGAAGTTGCATCTACCTGTGCATTGTCTAGTCGACTGTGATCCATATGGCTTTGAGATCCTAGCCACATACCGTTTTGGCTCCATGGTTAGATTCTGTTACAAAATATAG
Protein Sequence
- >AT3G13170.3
MEGKFAISESTNLLQRIKDFTQSVVVDLAEGRSPKISINQFRNYCMNPEADCLCSSDKPKGQEIFTLKKEPQTYRIDMLLRVLLIVQQLLQENRHASKRDIYYMHPSAFKAQSIVDRAIGDICILFQCSRYNLNVVSVGNGLVMGWLKFREAGRKFDCLNSLNTAYPVPVLVEEVEDIVSLAEYILVVEKETVFQRLANDMFCKTNRCIVITGRGYPDVSTRRFLRLLMEKLHLPVHCLVDCDPYGFEILATYRFGSMVRFCYKI - >AT3G13170.2
MEGKFAISESTNLLQRIKDFTQSVVVDLAEGRSPKISINQFRNYCMNPEADCLCSSDKPKGQEIFTLKKEPQTYRIDMLLRVLLIVQQLLQENRHASKRDIYYMHPSAFKAQSIVDRAIGDICILFQCSRYNLNVVSVGNGLVMGWLKFREAGRKFDCLNSLNTAYPVPVLVEEVEDIVSLAEYILVVEKETVFQRLANDMFCKTNRCIVITGRGYPDVSTRRFLRLLMEKLHLPVHCLVDCDPYGFEILATYRFGSMVRFCYKI - >AT3G13170.1
MEGKFAISESTNLLQRIKDFTQSVVVDLAEGRSPKISINQFRNYCMNPEADCLCSSDKPKGQEIFTLKKEPQTYRIDMLLRVLLIVQQLLQENRHASKRDIYYMHPSAFKAQSIVDRAIGDICILFQCSRYNLNVVSVGNGLVMGWLKFREAGRKFDCLNSLNTAYPVPVLVEEVEDIVSLAEYILVVEKETVFQRLANDMFCKTNRCIVITGRGYPDVSTRRFLRLLMEKLHLPVHCLVDCDPYGFEILATYRFGSMVRFCYKI