Information report for AT2G41370
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:0000146 — abscission zone — zona de absición (Spanish, exact), 離層 (Japanese, exact), abscission layer (related)
- PO:0000229 — flower meristem — floral meristem (exact), mersitema floral (Spanish, exact), 花芽分裂組織 (Japanese, exact), floral apical meristem (related), Poaceae floret meristem (narrow), ear floret meristem (narrow), floret meristem (narrow), tassel floret meristem (narrow)
- PO:0009005 — root — raíz (Spanish, exact), radices (exact, plural), radix (exact), 根 (Japanese, exact), aerial root (narrow), climbing root (narrow)
- PO:0009025 — vascular leaf — foliage leaf (exact), hoja vascular (Spanish, exact), leaf, vascular (exact), vascular leaves (exact, plural), 維管束のある葉, または維管束植物の葉 (Japanese, exact), crozier (related), macrophyll (related), megaphyll (related), ascidia (narrow), ascidium (narrow), fiddlehead (narrow), frond (narrow), needle-like leaf (narrow), pitcher (narrow), pitcher blade (narrow), pitcher-blade (narrow), scale-like leaf (narrow), sterile frond (narrow), trophophyll (narrow)
- 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:0009047 — stem — caña (Spanish, exact), culm (exact), eje primario (Spanish, exact), primary axis (exact), primary stem (exact), tallo (Spanish, exact), tronco (Spanish, exact), 茎 (Japanese, exact), bole (narrow), cane (narrow), caudex (narrow), caudices (narrow), core (narrow), primocane (narrow), scape (narrow), stalk (narrow), trunk (narrow)
- PO:0009006 — shoot system — sistema de epiblasto (epiblastema) (Spanish, exact), シュート系、苗条系 (Japanese, exact), Poaceae crown (related), shoot (related), thalli (related), thallus (related), tree crown (narrow)
- PO:0009009 — plant embryo — embrión (Spanish, exact), 植物胚 (Japanese, exact), germ (related), embryo (broad)
- PO:0009031 — sepal — sépalo (Spanish, exact), がく片 (Japanese, exact)
- PO:0020030 — cotyledon — cotiledón (Spanish, exact), seed leaf (exact), 子葉 (Japanese, exact)
- PO:0020100 — hypocotyl — hipocótile (Spanish, exact), 胚軸 (Japanese, exact)
- PO:0020137 — leaf apex — ápice de la hoja (Spanish, exact), 葉先 (Japanese, exact), leaf lamina apex (narrow), phyllid apex (narrow)
- PO:0025022 — collective leaf structure — estructura colectiva de hoja (Spanish, exact), leaf series (exact), 葉が集まった構造 (Japanese, exact), leaf whorl (narrow), rosette (narrow), cycle (broad), verticil (broad)
- PO:0025228 — valve — valva (Spanish, exact), 弁 (Japanese, exact)
- CS69935 — Developmental defects affecting the morphological symmetry of leaves and flowers. Abnormally long leaves, cauline leaves with serrated bases, leafy petioles, extra abaxial floral organs, formation of an ectopic floral bract, and loss of floral organ abscission.
- bop1-3/bop2-1 — Abnormal abscission zone anatomy. Lacks nectaries. Floral organ abscission defective.
- bop1-3/bop2-1 — Double mutant of related genes indicates redundant function in leaf and flower development. Leaves are elongated and indeterminate, floral organ number is increased. Also shows absence of floral organ abscission.
- bop1-4 bop2-11 — Double mutant inflorescences displayed slightly enhanced phenotypes compared with those of either single mutant.
- bop1-4 bop2-11 — Double mutant plants displayed an enhanced cauline leaf outgrowth phenotype compared with bop1-4 plants.
- bop1-4 bop2-11 — LBD36/ASL1 transcript levels were not reduced in bop1-4 bop2-11 plants.
- bop1-4 bop2-11 — Mutant leaf petioles displayed clusters of densely cytoplasmic, undifferentiated cells on the adaxial side, coincident with the development of ectopic outgrowths.
- bop1-4 bop2-11 — Mutant plants developed extensive ectopic blade outgrowths along the rosette leaf petiole, like those observed in homozygous bop1-1 plants.
- bop1-4 bop2-11 — The stem vasculature in bop1 bop2 plants showed normal vein morphology.
- bop1-4 bop2-11 — Whereas the gynoecium of wild-type flowers consists of two fused carpels ~50% of bop1-4 bop2-11 gynoecia contained only a single, fertile carpel.
- bop1-4 bop2-11 as1-1 — Mutant leaf petioles displayed clusters of densely cytoplasmic, undifferentiated cells on the adaxial side, coincident with the development of ectopic outgrowths.
- bop1-4 bop2-11 as1-1 — The rosette leaf petioles of the triple mutant plants showed extensive ectopic outgrowth formation in the marginal region, and some outgrowths exhibited a strongly radialized character.
- bop1-4 bop2-11 as1-1 — The vascular patterning defects in the triple mutant leaf petioles were greatly enhanced compared with those of the parental plants.
- bop1-4 bop2-11 as2-1 — Mutant leaf petioles displayed clusters of densely cytoplasmic, undifferentiated cells on the adaxial side, coincident with the development of ectopic outgrowths.
- bop1-4 bop2-11 as2-1 — The rosette leaf petioles of the triple mutant plants showed extensive ectopic outgrowth formation in the marginal region, and some outgrowths exhibited a strongly radialized character.
- bop1-4 bop2-11 as2-1 — The vascular patterning defects in the triple mutant leaf petioles were greatly enhanced compared with those of the parental plants.
- bop1-4 bop2-11 kan1-2 kan2-1 — About nine-tenths of the mutants exhibited abaxialized vasculature. The exclusively adaxialized vasculature observed in kan1 kan2 petioles was not detected in bop1 bop2 kan1 kan2 petioles. The radialized portion of bop1 bop2 kan1 kan2 leaves showed various kinds of organ polarity defects. The vascular bundles of nearly half of the leaves (44.0%) consisted of phloem surrounded by xylem, while one-third (36.0%) displayed xylem surrounded by phloem, and a small percentage (16.0%) had a mixture of both types of vasculature.
- bop1-4 bop2-11 kan1-2 kan2-1 — Quadruple mutant plants developed narrow leaves with ectopic blade outgrowth along the petioles, like bop1 bop2 leaves, as well as ectopic outgrowths on their abaxial lamina, like kan1 kan2 leaves. However, all of the bop1 bop2 kan1 kan2 leaves also showed extended, radialized petiole development that was not observed in either parental genotype.
- bop1-4 bop2-11 kan1-2 kan2-1 — bop1 bop2 kan1 kan2 stems had a decreased ratio of adaxialized vascular phenotypes compared with kan1 kan2 stems. Similar to what was observed in petioles, 6.7% of bop1 bop2 kan1 kan2 stems exhibited an abaxialized phenotype of xylem surrounded by phloem, while others (13.3%) had both types of vasculature in a single stem.
- bop2-11 — Cauline leaves of bop2 plants do not develop ectopic outgrowths from the basal region.
- bop2-11 — Plants displayed defects in inflorescence development.
- bop2-11 — Plants frequently formed fused and/or fasciated inflorescences and generated multiple flowers from the same node.
Functional Keywords
- shoot axis apex , abscission zone , flower meristem , root , vascular leaf , flower , stem , shoot axis apex , root , shoot system , plant embryo , vascular leaf , sepal , flower , cotyledon , hypocotyl , leaf apex , collective leaf structure , valve
Literature and News
- An Arabidopsis NPR1-like gene, NPR4, is required for disease resistance. DOI: 10.1111/j.1365-313X.2004.02296.x ; PMID: 15634206
- BLADE-ON-PETIOLE-dependent signaling controls leaf and floral patterning in Arabidopsis. DOI: 10.1105/tpc.104.030536 ; PMID: 15805484
- The BLADE ON PETIOLE genes act redundantly to control the growth and development of lateral organs. DOI: 10.1242/dev.01815 ; PMID: 15800002
- BLADE-ON-PETIOLE 1 and 2 control Arabidopsis lateral organ fate through regulation of LOB domain and adaxial-abaxial polarity genes. DOI: 10.1105/tpc.107.051938 ; PMID: 17601823
- The BLADE-ON-PETIOLE genes are essential for abscission zone formation in Arabidopsis. DOI: 10.1242/dev.012807 ; PMID: 18339677
- A role for Arabidopsis PUCHI in floral meristem identity and bract suppression. DOI: 10.1105/tpc.109.067025 ; PMID: 19482972
- BLADE-ON-PETIOLE1 coordinates organ determinacy and axial polarity in arabidopsis by directly activating ASYMMETRIC LEAVES2. DOI: 10.1105/tpc.109.070763 ; PMID: 20118228
- Arabidopsis BLADE-ON-PETIOLE1 and 2 promote floral meristem fate and determinacy in a previously undefined pathway targeting APETALA1 and AGAMOUS-LIKE24. DOI: 10.1111/j.1365-313X.2010.04299.x ; PMID: 20626659
- Control of Arabidopsis leaf morphogenesis through regulation of the YABBY and KNOX families of transcription factors. DOI: 10.1534/genetics.110.118703 ; PMID: 20610407
- MicroRNA534a control of BLADE-ON-PETIOLE 1 and 2 mediates juvenile-to-adult gametophyte transition in Physcomitrella patens. DOI: 10.1111/j.1365-313X.2010.04451.x ; PMID: 21235646
- The MADS box gene, FOREVER YOUNG FLOWER, acts as a repressor controlling floral organ senescence and abscission in Arabidopsis. DOI: 10.1111/j.1365-313X.2011.04677.x ; PMID: 21689171
- Antagonistic interaction of BLADE-ON-PETIOLE1 and 2 with BREVIPEDICELLUS and PENNYWISE regulates Arabidopsis inflorescence architecture. DOI: 10.1104/pp.111.188573 ; PMID: 22114095
- BLADE-ON-PETIOLE1 and 2 regulate Arabidopsis inflorescence architecture in conjunction with homeobox genes KNAT6 and ATH1. DOI: 10.4161/psb.20599 ; PMID: 22751300
- A novel approach to dissect the abscission process in Arabidopsis. DOI: 10.1104/pp.112.205955 ; PMID: 22992509
- The BLADE-ON-PETIOLE genes of Arabidopsis are essential for resistance induced by methyl jasmonate. DOI: 10.1186/1471-2229-12-199 ; PMID: 23116333
- Class I KNOX transcription factors promote differentiation of cambial derivatives into xylem fibers in the Arabidopsis hypocotyl. DOI: 10.1242/dev.111369 ; PMID: 25371365
- An Arabidopsis gene regulatory network for secondary cell wall synthesis. DOI: 10.1038/nature14099 ; PMID: 25533953
- The barley Uniculme4 gene encodes a BLADE-ON-PETIOLE-like protein that controls tillering and leaf patterning. DOI: 10.1104/pp.114.252882 ; PMID: 25818702
- Floral Induction in Arabidopsis by FLOWERING LOCUS T Requires Direct Repression of BLADE-ON-PETIOLE Genes by the Homeodomain Protein PENNYWISE. DOI: 10.1104/pp.15.00960 ; PMID: 26417007
- HANABA TARANU (HAN) Bridges Meristem and Organ Primordia Boundaries through PINHEAD, JAGGED, BLADE-ON-PETIOLE2 and CYTOKININ OXIDASE 3 during Flower Development in Arabidopsis. DOI: 10.1371/journal.pgen.1005479 ; PMID: 26390296
- A Homolog of Blade-On-Petiole 1 and 2 (BOP1/2) Controls Internode Length and Homeotic Changes of the Barley Inflorescence. DOI: 10.1104/pp.16.00124 ; PMID: 27208226
- BLADE-ON-PETIOLE proteins act in an E3 ubiquitin ligase complex to regulate PHYTOCHROME INTERACTING FACTOR 4 abundance. DOI: 10.7554/eLife.26759 ; PMID: 28826468
- DORNRÖSCHEN, DORNRÖSCHEN-LIKE, and PUCHI redundantly control floral meristem identity and organ initiation in Arabidopsis. DOI: 10.1093/jxb/erx208 ; PMID: 28859377
- LEAFY activity is post-transcriptionally regulated by BLADE ON PETIOLE2 and CULLIN3 in Arabidopsis. DOI: 10.1111/nph.15329 ; PMID: 29995985
- Clade I TGACG-Motif Binding Basic Leucine Zipper Transcription Factors Mediate BLADE-ON-PETIOLE-Dependent Regulation of Development. DOI: 10.1104/pp.18.00805 ; PMID: 30923069
- ARABIDOPSIS THALIANA HOMEOBOX GENE 1 controls plant architecture by locally restricting environmental responses. DOI: 10.1073/pnas.2018615118 ; PMID: 33888582
- Transcriptional landscapes of de novo root regeneration from detached Arabidopsis leaves revealed by time-lapse and single-cell RNA sequencing analyses. DOI: 10.1016/j.xplc.2022.100306 ; PMID: 35605192
- Floral organ abscission in Arabidopsis requires the combined activities of three TALE homeodomain transcription factors. DOI: 10.1093/jxb/erac255 ; PMID: 35689803
- and noncell-autonomous AUXIN RESPONSE FACTOR3 controls meristem proliferation and phyllotactic patterns. DOI: 10.1093/plphys/kiac370 ; PMID: 35972411
- SQUAMOSA PROMOTER BINDING PROTEIN-LIKE 9 and 13 repress BLADE-ON-PETIOLE 1 and 2 directly to promote adult leaf morphology in Arabidopsis. DOI: 10.1093/jxb/erad017 ; PMID: 36629519
- Arabidopsis BLADE-ON-PETIOLE1 and 2 promote floral meristem fate and determinacy in a previously undefined pathway targeting APETALA1 and AGAMOUS-LIKE24. DOI: 10.1111/j.1365-313X.2010.04299.x ; PMID: 20626659
Gene Resources
Homologs
- Oryza sativa OsBOP1, OsBOP3, OsBOP2, NH3;OsNPR3, OsNPR1;NH1
Sequences
cDNA Sequence
- >AT2G41370.1
AAACACTGAAACAGTTATAATTTTTTTTTAACCATCTTAGTTTAAATATCTGAGCCGCCCGGTTCATCCATTCAAATCTCTCTCTCACTTACCAAACCCAAACAAATATCTAACACCACAAACTCAAAGCAATAAAGAATCCTTCTCTCTCTCTCTTTCTTTCTTTCTTCTTTCAGAGAGGAGGAGCAAGAAAGAAGCTTCAAAAGAACAAAGCTTAAGCTTTTTCCCCCGGAAAATTTGTTCCCCTTTTTCGAAAAACTAATAATTCGTAACTTCATAGCCAACAAGATCAATAAAAGGAGGCAACTTATTTCTTTCATTCTCTCTTGTAAAGAGTACTTGCTAAACCCTAGCTTTTGTTCTATAGAGAATCCAAGAACCAATCAATTTTTTATTTTATAAAAAGATGAGCAATCTTGAAGAATCTTTGAGATCTCTATCGTTGGATTTCCTGAACCTACTAATCAACGGTCAAGCTTTCTCCGACGTGACTTTCAGCGTTGAAGGTCGTTTAGTCCACGCTCACCGTTGTATCCTCGCCGCACGGAGTCTTTTCTTCCGCAAATTCTTTTGTGGGACAGACTCACCACAACCTGTCACAGGTATAGACCCGACCCAACATGGGTCCGTACCCGCTAGCCCAACAAGAGGCTCCACGGCCCCAGCTGGAATTATACCAGTGAACTCAGTCGGTTATGAGGTTTTTCTGTTGCTACTTCAGTTTCTTTATAGCGGACAAGTCTCCATCGTGCCGCAGAAACACGAGCCTAGACCTAATTGTGGCGAGAGAGGATGTTGGCACACTCATTGCTCAGCCGCCGTTGATCTTGCTCTTGATACTCTCGCCGCCTCTCGTTACTTCGGCGTCGAGCAGCTCGCATTGCTCACCCAGAAACAATTGGCAAGCATGGTGGAGAAAGCCTCTATCGAAGATGTGATGAAAGTTTTAATAGCATCAAGAAAGCAAGACATGCATCAATTATGGACCACCTGCTCTCACTTAGTTGCTAAATCAGGTCTCCCACCAGAGATTCTTGCCAAGCATCTCCCTATTGACGTCGTCACCAAAATAGAAGAGCTTCGTCTTAAATCTTCTATAGCTCGCCGTTCTCTAATGCCTCACAACCACCACCATGATCTCAGCGTGGCTCAAGACCTAGAAGATCAAAAGATTAGAAGGATGAGACGAGCTTTGGATTCATCAGACGTGGAACTAGTGAAGCTGATGGTAATGGGAGAAGGACTCAATCTTGATGAGTCGTTAGCATTGCATTACGCTGTTGAAAGCTGTAGTAGAGAAGTTGTGAAGGCTTTGCTTGAGCTTGGAGCTGCCGATGTGAATTATCCGGCGGGTCCGGCAGGGAAAACACCTTTGCACATCGCGGCTGAGATGGTCTCTCCAGACATGGTGGCTGTTCTGTTAGACCACCATGCTGATCCTAATGTGAGGACAGTTGGTGGAATCACGCCTCTTGATATCCTTAGAACATTAACTTCGGATTTCTTGTTCAAGGGGGCAGTTCCTGGATTGACTCACATTGAACCGAATAAACTTAGGCTTTGCCTCGAGCTTGTTCAATCCGCTGCAATGGTGATATCTCGAGAAGAAGGAAACAATAGCAACAACCAAAACAATGATAACAATACCGGGATTTACCCTCATATGAATGAGGAGCACAATAGTGGAAGCAGTGGAGGGAGCAATAACAATTTGGATTCAAGATTGGTTTATCTCAATCTTGGAGCAGGTACGGGTCAGATGGGTCCAGGTCGAGATCAAGGGGATGACCATAACAGTCAGAGGGAAGGTATGAGTCGGCATCATCATCATCATCAAGACCCATCTACAATGTATCATCACCATCATCAACATCACTTCTAGTTCTCTATATTGGTCTCTATATCTCAACCATATAAGACTCAAAATAAATTTATTAATTTAGTTCTTATATCTTCTATATTTATTTCTGTATATGGAAATTAATGAGGACATATAAGGAGAGTATTAAGAAGAGGGGCATGCAGGAATTTAAGATCATGCATCCGTTATATAATTATAGACTAGGTTTATTTAAATTAGTTGCTCTAGCTATCGCTCATCGTTGTACTAATTAATCATTTGATTAACTTTGCCATCGATTAATATCTTATCTTTATACCCTAATTTCTTCCTA
CDS Sequence
- >AT2G41370.1
ATGAGCAATCTTGAAGAATCTTTGAGATCTCTATCGTTGGATTTCCTGAACCTACTAATCAACGGTCAAGCTTTCTCCGACGTGACTTTCAGCGTTGAAGGTCGTTTAGTCCACGCTCACCGTTGTATCCTCGCCGCACGGAGTCTTTTCTTCCGCAAATTCTTTTGTGGGACAGACTCACCACAACCTGTCACAGGTATAGACCCGACCCAACATGGGTCCGTACCCGCTAGCCCAACAAGAGGCTCCACGGCCCCAGCTGGAATTATACCAGTGAACTCAGTCGGTTATGAGGTTTTTCTGTTGCTACTTCAGTTTCTTTATAGCGGACAAGTCTCCATCGTGCCGCAGAAACACGAGCCTAGACCTAATTGTGGCGAGAGAGGATGTTGGCACACTCATTGCTCAGCCGCCGTTGATCTTGCTCTTGATACTCTCGCCGCCTCTCGTTACTTCGGCGTCGAGCAGCTCGCATTGCTCACCCAGAAACAATTGGCAAGCATGGTGGAGAAAGCCTCTATCGAAGATGTGATGAAAGTTTTAATAGCATCAAGAAAGCAAGACATGCATCAATTATGGACCACCTGCTCTCACTTAGTTGCTAAATCAGGTCTCCCACCAGAGATTCTTGCCAAGCATCTCCCTATTGACGTCGTCACCAAAATAGAAGAGCTTCGTCTTAAATCTTCTATAGCTCGCCGTTCTCTAATGCCTCACAACCACCACCATGATCTCAGCGTGGCTCAAGACCTAGAAGATCAAAAGATTAGAAGGATGAGACGAGCTTTGGATTCATCAGACGTGGAACTAGTGAAGCTGATGGTAATGGGAGAAGGACTCAATCTTGATGAGTCGTTAGCATTGCATTACGCTGTTGAAAGCTGTAGTAGAGAAGTTGTGAAGGCTTTGCTTGAGCTTGGAGCTGCCGATGTGAATTATCCGGCGGGTCCGGCAGGGAAAACACCTTTGCACATCGCGGCTGAGATGGTCTCTCCAGACATGGTGGCTGTTCTGTTAGACCACCATGCTGATCCTAATGTGAGGACAGTTGGTGGAATCACGCCTCTTGATATCCTTAGAACATTAACTTCGGATTTCTTGTTCAAGGGGGCAGTTCCTGGATTGACTCACATTGAACCGAATAAACTTAGGCTTTGCCTCGAGCTTGTTCAATCCGCTGCAATGGTGATATCTCGAGAAGAAGGAAACAATAGCAACAACCAAAACAATGATAACAATACCGGGATTTACCCTCATATGAATGAGGAGCACAATAGTGGAAGCAGTGGAGGGAGCAATAACAATTTGGATTCAAGATTGGTTTATCTCAATCTTGGAGCAGGTACGGGTCAGATGGGTCCAGGTCGAGATCAAGGGGATGACCATAACAGTCAGAGGGAAGGTATGAGTCGGCATCATCATCATCATCAAGACCCATCTACAATGTATCATCACCATCATCAACATCACTTCTAG
Protein Sequence
- >AT2G41370.1
MSNLEESLRSLSLDFLNLLINGQAFSDVTFSVEGRLVHAHRCILAARSLFFRKFFCGTDSPQPVTGIDPTQHGSVPASPTRGSTAPAGIIPVNSVGYEVFLLLLQFLYSGQVSIVPQKHEPRPNCGERGCWHTHCSAAVDLALDTLAASRYFGVEQLALLTQKQLASMVEKASIEDVMKVLIASRKQDMHQLWTTCSHLVAKSGLPPEILAKHLPIDVVTKIEELRLKSSIARRSLMPHNHHHDLSVAQDLEDQKIRRMRRALDSSDVELVKLMVMGEGLNLDESLALHYAVESCSREVVKALLELGAADVNYPAGPAGKTPLHIAAEMVSPDMVAVLLDHHADPNVRTVGGITPLDILRTLTSDFLFKGAVPGLTHIEPNKLRLCLELVQSAAMVISREEGNNSNNQNNDNNTGIYPHMNEEHNSGSSGGSNNNLDSRLVYLNLGAGTGQMGPGRDQGDDHNSQREGMSRHHHHHQDPSTMYHHHHQHHF