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BRX_ARATH
ID   BRX_ARATH               Reviewed;         344 AA.
AC   Q17TI5; Q17TI6; Q84JB6; Q9C6S9;
DT   05-MAY-2009, integrated into UniProtKB/Swiss-Prot.
DT   05-MAY-2009, sequence version 2.
DT   03-AUG-2022, entry version 77.
DE   RecName: Full=Protein BREVIS RADIX {ECO:0000303|PubMed:15031265};
DE            Short=AtBRX {ECO:0000303|PubMed:15031265};
GN   Name=BRX {ECO:0000303|PubMed:15031265};
GN   OrderedLocusNames=At1g31880 {ECO:0000312|Araport:AT1G31880};
GN   ORFNames=F5M6.11 {ECO:0000312|EMBL:AAG50720.1};
OS   Arabidopsis thaliana (Mouse-ear cress).
OC   Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;
OC   Spermatophyta; Magnoliopsida; eudicotyledons; Gunneridae; Pentapetalae;
OC   rosids; malvids; Brassicales; Brassicaceae; Camelineae; Arabidopsis.
OX   NCBI_TaxID=3702;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA], FUNCTION, AND SUBCELLULAR LOCATION.
RC   STRAIN=cv. Uk-1, and cv. Uk-2;
RX   PubMed=15031265; DOI=10.1101/gad.1187704;
RA   Mouchel C.F., Briggs G.C., Hardtke C.S.;
RT   "Natural genetic variation in Arabidopsis identifies BREVIS RADIX, a novel
RT   regulator of cell proliferation and elongation in the root.";
RL   Genes Dev. 18:700-714(2004).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=cv. Columbia;
RX   PubMed=11130712; DOI=10.1038/35048500;
RA   Theologis A., Ecker J.R., Palm C.J., Federspiel N.A., Kaul S., White O.,
RA   Alonso J., Altafi H., Araujo R., Bowman C.L., Brooks S.Y., Buehler E.,
RA   Chan A., Chao Q., Chen H., Cheuk R.F., Chin C.W., Chung M.K., Conn L.,
RA   Conway A.B., Conway A.R., Creasy T.H., Dewar K., Dunn P., Etgu P.,
RA   Feldblyum T.V., Feng J.-D., Fong B., Fujii C.Y., Gill J.E., Goldsmith A.D.,
RA   Haas B., Hansen N.F., Hughes B., Huizar L., Hunter J.L., Jenkins J.,
RA   Johnson-Hopson C., Khan S., Khaykin E., Kim C.J., Koo H.L.,
RA   Kremenetskaia I., Kurtz D.B., Kwan A., Lam B., Langin-Hooper S., Lee A.,
RA   Lee J.M., Lenz C.A., Li J.H., Li Y.-P., Lin X., Liu S.X., Liu Z.A.,
RA   Luros J.S., Maiti R., Marziali A., Militscher J., Miranda M., Nguyen M.,
RA   Nierman W.C., Osborne B.I., Pai G., Peterson J., Pham P.K., Rizzo M.,
RA   Rooney T., Rowley D., Sakano H., Salzberg S.L., Schwartz J.R., Shinn P.,
RA   Southwick A.M., Sun H., Tallon L.J., Tambunga G., Toriumi M.J., Town C.D.,
RA   Utterback T., Van Aken S., Vaysberg M., Vysotskaia V.S., Walker M., Wu D.,
RA   Yu G., Fraser C.M., Venter J.C., Davis R.W.;
RT   "Sequence and analysis of chromosome 1 of the plant Arabidopsis thaliana.";
RL   Nature 408:816-820(2000).
RN   [3]
RP   GENOME REANNOTATION.
RC   STRAIN=cv. Columbia;
RX   PubMed=27862469; DOI=10.1111/tpj.13415;
RA   Cheng C.Y., Krishnakumar V., Chan A.P., Thibaud-Nissen F., Schobel S.,
RA   Town C.D.;
RT   "Araport11: a complete reannotation of the Arabidopsis thaliana reference
RT   genome.";
RL   Plant J. 89:789-804(2017).
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   STRAIN=cv. Columbia;
RX   PubMed=14593172; DOI=10.1126/science.1088305;
RA   Yamada K., Lim J., Dale J.M., Chen H., Shinn P., Palm C.J., Southwick A.M.,
RA   Wu H.C., Kim C.J., Nguyen M., Pham P.K., Cheuk R.F., Karlin-Newmann G.,
RA   Liu S.X., Lam B., Sakano H., Wu T., Yu G., Miranda M., Quach H.L.,
RA   Tripp M., Chang C.H., Lee J.M., Toriumi M.J., Chan M.M., Tang C.C.,
RA   Onodera C.S., Deng J.M., Akiyama K., Ansari Y., Arakawa T., Banh J.,
RA   Banno F., Bowser L., Brooks S.Y., Carninci P., Chao Q., Choy N., Enju A.,
RA   Goldsmith A.D., Gurjal M., Hansen N.F., Hayashizaki Y., Johnson-Hopson C.,
RA   Hsuan V.W., Iida K., Karnes M., Khan S., Koesema E., Ishida J., Jiang P.X.,
RA   Jones T., Kawai J., Kamiya A., Meyers C., Nakajima M., Narusaka M.,
RA   Seki M., Sakurai T., Satou M., Tamse R., Vaysberg M., Wallender E.K.,
RA   Wong C., Yamamura Y., Yuan S., Shinozaki K., Davis R.W., Theologis A.,
RA   Ecker J.R.;
RT   "Empirical analysis of transcriptional activity in the Arabidopsis
RT   genome.";
RL   Science 302:842-846(2003).
RN   [5]
RP   TISSUE SPECIFICITY, AND INDUCTION BY AUXIN AND BRASSINOLIDE.
RX   PubMed=17006513; DOI=10.1038/nature05130;
RA   Mouchel C.F., Osmont K.S., Hardtke C.S.;
RT   "BRX mediates feedback between brassinosteroid levels and auxin signalling
RT   in root growth.";
RL   Nature 443:458-461(2006).
RN   [6]
RP   GENE FAMILY, DOMAIN, AND SUBUNIT.
RX   PubMed=16514016; DOI=10.1104/pp.105.075382;
RA   Briggs G.C., Mouchel C.F., Hardtke C.S.;
RT   "Characterization of the plant-specific BREVIS RADIX gene family reveals
RT   limited genetic redundancy despite high sequence conservation.";
RL   Plant Physiol. 140:1306-1316(2006).
RN   [7]
RP   FUNCTION, SUBCELLULAR LOCATION, DEVELOPMENTAL STAGE, AND INTERACTION WITH
RP   NGA1.
RX   PubMed=19465596; DOI=10.1242/dev.035444;
RA   Scacchi E., Osmont K.S., Beuchat J., Salinas P., Navarrete-Gomez M.,
RA   Trigueros M., Ferrandiz C., Hardtke C.S.;
RT   "Dynamic, auxin-responsive plasma membrane-to-nucleus movement of
RT   Arabidopsis BRX.";
RL   Development 136:2059-2067(2009).
RN   [8]
RP   DISRUPTION PHENOTYPE.
RX   PubMed=19037657; DOI=10.1007/s00425-008-0854-6;
RA   Li J., Mo X., Wang J., Chen N., Fan H., Dai C., Wu P.;
RT   "BREVIS RADIX is involved in cytokinin-mediated inhibition of lateral root
RT   initiation in Arabidopsis.";
RL   Planta 229:593-603(2009).
RN   [9]
RP   FUNCTION, DISRUPTION PHENOTYPE, AND TISSUE SPECIFICITY.
RX   PubMed=19201913; DOI=10.1104/pp.108.133819;
RA   Rodrigues A., Santiago J., Rubio S., Saez A., Osmont K.S., Gadea J.,
RA   Hardtke C.S., Rodriguez P.L.;
RT   "The short-rooted phenotype of the brevis radix mutant partly reflects root
RT   abscisic acid hypersensitivity.";
RL   Plant Physiol. 149:1917-1928(2009).
RN   [10]
RP   FUNCTION, TISSUE SPECIFICITY, AND DISRUPTION PHENOTYPE.
RX   PubMed=20649916; DOI=10.1111/j.1469-8137.2010.03387.x;
RA   Beuchat J., Scacchi E., Tarkowska D., Ragni L., Strnad M., Hardtke C.S.;
RT   "BRX promotes Arabidopsis shoot growth.";
RL   New Phytol. 188:23-29(2010).
RN   [11]
RP   FUNCTION, TISSUE SPECIFICITY, AND INTERACTION WITH ARF5.
RX   PubMed=21149702; DOI=10.1073/pnas.1014716108;
RA   Scacchi E., Salinas P., Gujas B., Santuari L., Krogan N., Ragni L.,
RA   Berleth T., Hardtke C.S.;
RT   "Spatio-temporal sequence of cross-regulatory events in root meristem
RT   growth.";
RL   Proc. Natl. Acad. Sci. U.S.A. 107:22734-22739(2010).
RN   [12]
RP   FUNCTION, DISRUPTION PHENOTYPE, DEVELOPMENTAL STAGE, AND TISSUE
RP   SPECIFICITY.
RC   STRAIN=cv. Columbia;
RX   PubMed=23569225; DOI=10.1073/pnas.1222314110;
RA   Depuydt S., Rodriguez-Villalon A., Santuari L., Wyser-Rmili C., Ragni L.,
RA   Hardtke C.S.;
RT   "Suppression of Arabidopsis protophloem differentiation and root meristem
RT   growth by CLE45 requires the receptor-like kinase BAM3.";
RL   Proc. Natl. Acad. Sci. U.S.A. 110:7074-7079(2013).
RN   [13]
RP   FUNCTION, DISRUPTION PHENOTYPE, AND TISSUE SPECIFICITY.
RC   STRAIN=cv. Columbia;
RX   PubMed=25049386; DOI=10.1073/pnas.1407337111;
RA   Rodriguez-Villalon A., Gujas B., Kang Y.H., Breda A.S., Cattaneo P.,
RA   Depuydt S., Hardtke C.S.;
RT   "Molecular genetic framework for protophloem formation.";
RL   Proc. Natl. Acad. Sci. U.S.A. 111:11551-11556(2014).
RN   [14]
RP   DISRUPTION PHENOTYPE.
RC   STRAIN=cv. Columbia;
RX   PubMed=27354416; DOI=10.15252/embr.201642450;
RA   Kang Y.H., Hardtke C.S.;
RT   "Arabidopsis MAKR5 is a positive effector of BAM3-dependent CLE45
RT   signaling.";
RL   EMBO Rep. 17:1145-1154(2016).
RN   [15]
RP   FUNCTION, DISRUPTION PHENOTYPE, AND SUBCELLULAR LOCATION.
RC   STRAIN=cv. Columbia;
RX   PubMed=28652362; DOI=10.1073/pnas.1703258114;
RA   Breda A.S., Hazak O., Hardtke C.S.;
RT   "Phosphosite charge rather than shootward localization determines OCTOPUS
RT   activity in root protophloem.";
RL   Proc. Natl. Acad. Sci. U.S.A. 114:E5721-E5730(2017).
CC   -!- FUNCTION: Acts as a regulator of cell proliferation and elongation in
CC       the root and shoot (PubMed:25049386, PubMed:28652362). Regulates roots
CC       architecture and primary root protophloem differentiation
CC       (PubMed:25049386, PubMed:28652362). BRX, BAM3, and CLE45 act together
CC       to regulate the transition of protophloem cells from proliferation to
CC       differentiation, thus impinging on postembryonic growth capacity of the
CC       root meristem (PubMed:23569225). Probable transcription regulator.
CC       Regulated by the auxin response factor ARF5. Polarly localized in
CC       vascular cells and subject to endocytic recycling. Required for CPD
CC       expression and for correct nuclear auxin response. Mediates cross-talk
CC       between the auxin and brassinosteroid pathways. BRX is a target for
CC       auxin-induced, proteasome-mediated degradation.
CC       {ECO:0000269|PubMed:15031265, ECO:0000269|PubMed:19201913,
CC       ECO:0000269|PubMed:19465596, ECO:0000269|PubMed:20649916,
CC       ECO:0000269|PubMed:21149702, ECO:0000269|PubMed:23569225,
CC       ECO:0000269|PubMed:25049386, ECO:0000269|PubMed:28652362}.
CC   -!- SUBUNIT: Homodimer and heterodimer with BRXL1. Interacts with NGA1 and
CC       ARF5. {ECO:0000269|PubMed:16514016, ECO:0000269|PubMed:19465596,
CC       ECO:0000269|PubMed:21149702}.
CC   -!- INTERACTION:
CC       Q17TI5; Q9S7Z2: AFP4; NbExp=3; IntAct=EBI-4426649, EBI-1778843;
CC       Q17TI5; Q9FLI3: AHG1; NbExp=3; IntAct=EBI-4426649, EBI-2363348;
CC       Q17TI5; Q8LPN5: AHL12; NbExp=3; IntAct=EBI-4426649, EBI-4428689;
CC       Q17TI5; Q9LKL2: APRR1; NbExp=3; IntAct=EBI-4426649, EBI-618423;
CC       Q17TI5; Q8L9Y3: ARR14; NbExp=3; IntAct=EBI-4426649, EBI-1100737;
CC       Q17TI5; Q949T8: ASHR3; NbExp=3; IntAct=EBI-4426649, EBI-4457339;
CC       Q17TI5; Q681Q7: At1g03900; NbExp=4; IntAct=EBI-4426649, EBI-4440643;
CC       Q17TI5; Q9SHJ1: At1g06460; NbExp=3; IntAct=EBI-4426649, EBI-25516773;
CC       Q17TI5; Q9FWW2: At1g12120; NbExp=3; IntAct=EBI-4426649, EBI-25518624;
CC       Q17TI5; A0A178WMH3: At1g23220; NbExp=3; IntAct=EBI-4426649, EBI-25519119;
CC       Q17TI5; Q9SLL2: At1g54200; NbExp=3; IntAct=EBI-4426649, EBI-25516987;
CC       Q17TI5; Q9SGS5: At1g76070; NbExp=3; IntAct=EBI-4426649, EBI-25519221;
CC       Q17TI5; O64764: At2g35010; NbExp=3; IntAct=EBI-4426649, EBI-25519089;
CC       Q17TI5; Q9LUS8: At3g16560; NbExp=3; IntAct=EBI-4426649, EBI-25519200;
CC       Q17TI5; Q9LS61: At3g18295; NbExp=3; IntAct=EBI-4426649, EBI-21457081;
CC       Q17TI5; F4JI72: At4g03250; NbExp=3; IntAct=EBI-4426649, EBI-15192535;
CC       Q17TI5; A0A1P8B4Y6: At4g21660; NbExp=3; IntAct=EBI-4426649, EBI-25519178;
CC       Q17TI5; Q9XFH9: At5g16400; NbExp=3; IntAct=EBI-4426649, EBI-25516100;
CC       Q17TI5; Q6NM33: At5g19340; NbExp=3; IntAct=EBI-4426649, EBI-25518939;
CC       Q17TI5; A0A178UKR9: At5g50180; NbExp=3; IntAct=EBI-4426649, EBI-25518767;
CC       Q17TI5; Q9LTI1: At5g59490; NbExp=3; IntAct=EBI-4426649, EBI-25518827;
CC       Q17TI5; A0A384LJI7: AXX17_At1g00240; NbExp=3; IntAct=EBI-4426649, EBI-25518871;
CC       Q17TI5; A0A178W725: AXX17_At1g45300; NbExp=3; IntAct=EBI-4426649, EBI-25515760;
CC       Q17TI5; A0A384KYS8: AXX17_At3g42630; NbExp=3; IntAct=EBI-4426649, EBI-25517043;
CC       Q17TI5; Q7XJU2: BHLH153; NbExp=5; IntAct=EBI-4426649, EBI-4427748;
CC       Q17TI5; Q9LEZ3: BIM1; NbExp=5; IntAct=EBI-4426649, EBI-617095;
CC       Q17TI5; Q9LDE2: BPC2; NbExp=3; IntAct=EBI-4426649, EBI-15215888;
CC       Q17TI5; Q9SGS4: CDSP32; NbExp=3; IntAct=EBI-4426649, EBI-25517863;
CC       Q17TI5; Q9SEZ7: CIPK16; NbExp=3; IntAct=EBI-4426649, EBI-1573415;
CC       Q17TI5; Q9MAM1: CIPK9; NbExp=4; IntAct=EBI-4426649, EBI-1765282;
CC       Q17TI5; Q9LFR7: CXE17; NbExp=5; IntAct=EBI-4426649, EBI-4456165;
CC       Q17TI5; Q9FG74: D6PK; NbExp=3; IntAct=EBI-4426649, EBI-1103570;
CC       Q17TI5; Q9SUA3: D6PKL1; NbExp=3; IntAct=EBI-4426649, EBI-1103605;
CC       Q17TI5; Q05999: D6PKL3; NbExp=4; IntAct=EBI-4426649, EBI-1103648;
CC       Q17TI5; O23263: dl3050c; NbExp=3; IntAct=EBI-4426649, EBI-25519155;
CC       Q17TI5; Q8GY79: DRB5; NbExp=3; IntAct=EBI-4426649, EBI-632672;
CC       Q17TI5; Q84MD6: DSP2; NbExp=6; IntAct=EBI-4426649, EBI-4424266;
CC       Q17TI5; Q56XH8: ECT11; NbExp=3; IntAct=EBI-4426649, EBI-25516971;
CC       Q17TI5; Q9FHK4: EDR4; NbExp=3; IntAct=EBI-4426649, EBI-1544548;
CC       Q17TI5; F4J6A1: EIF3G1; NbExp=3; IntAct=EBI-4426649, EBI-25518734;
CC       Q17TI5; Q9MAI5: ERF8; NbExp=3; IntAct=EBI-4426649, EBI-2000137;
CC       Q17TI5; Q9ZSZ8: FIP37; NbExp=4; IntAct=EBI-4426649, EBI-1641243;
CC       Q17TI5; Q9LYE4: FLZ10; NbExp=3; IntAct=EBI-4426649, EBI-25519036;
CC       Q17TI5; Q39103: GA3OX1; NbExp=5; IntAct=EBI-4426649, EBI-4426378;
CC       Q17TI5; F4KGE8: GIL1; NbExp=3; IntAct=EBI-4426649, EBI-25519238;
CC       Q17TI5; Q8LBK6: GRXS15; NbExp=3; IntAct=EBI-4426649, EBI-4427398;
CC       Q17TI5; Q9SAC6: GWD1; NbExp=3; IntAct=EBI-4426649, EBI-2355356;
CC       Q17TI5; Q9LZR5: HDT3; NbExp=3; IntAct=EBI-4426649, EBI-3387398;
CC       Q17TI5; Q9M4T3: HDT4; NbExp=3; IntAct=EBI-4426649, EBI-25518903;
CC       Q17TI5; Q9C9X7: IDD14; NbExp=3; IntAct=EBI-4426649, EBI-15191579;
CC       Q17TI5; Q948J9: LIP2P; NbExp=3; IntAct=EBI-4426649, EBI-25519006;
CC       Q17TI5; Q1H595: LSM2; NbExp=3; IntAct=EBI-4426649, EBI-9347308;
CC       Q17TI5; Q5XEN5: MBD1; NbExp=3; IntAct=EBI-4426649, EBI-4445335;
CC       Q17TI5; O80397: MKK4; NbExp=6; IntAct=EBI-4426649, EBI-2358409;
CC       Q17TI5; Q9C5C0: MPK18; NbExp=3; IntAct=EBI-4426649, EBI-1238534;
CC       Q17TI5; Q9SJG9: MPK20; NbExp=5; IntAct=EBI-4426649, EBI-2358896;
CC       Q17TI5; Q93ZM2: MWD9.9; NbExp=4; IntAct=EBI-4426649, EBI-4428808;
CC       Q17TI5; Q9SEZ4: MYB105; NbExp=3; IntAct=EBI-4426649, EBI-15202260;
CC       Q17TI5; Q9S9K9: MYB3; NbExp=3; IntAct=EBI-4426649, EBI-1786591;
CC       Q17TI5; Q8VYP8: MYJ24.12; NbExp=3; IntAct=EBI-4426649, EBI-4442894;
CC       Q17TI5; Q9FK59: NCBP; NbExp=3; IntAct=EBI-4426649, EBI-1770573;
CC       Q17TI5; O82799: NGA1; NbExp=6; IntAct=EBI-4426649, EBI-4427936;
CC       Q17TI5; P11035: NIA2; NbExp=3; IntAct=EBI-4426649, EBI-4451150;
CC       Q17TI5; Q9SWI1: PKS1; NbExp=3; IntAct=EBI-4426649, EBI-626200;
CC       Q17TI5; Q9M9T4: PKS2; NbExp=3; IntAct=EBI-4426649, EBI-25512733;
CC       Q17TI5; Q9FYE2: PKS4; NbExp=3; IntAct=EBI-4426649, EBI-25513821;
CC       Q17TI5; Q9S7H1: psaD1; NbExp=3; IntAct=EBI-4426649, EBI-1805558;
CC       Q17TI5; Q9C8D1: PUB20; NbExp=3; IntAct=EBI-4426649, EBI-25516153;
CC       Q17TI5; Q058P4: PUB30; NbExp=3; IntAct=EBI-4426649, EBI-4442587;
CC       Q17TI5; Q852U6: RHY1A; NbExp=4; IntAct=EBI-4426649, EBI-4428791;
CC       Q17TI5; Q8GY88: SK2; NbExp=3; IntAct=EBI-4426649, EBI-1238334;
CC       Q17TI5; Q0WT24: STOP2; NbExp=3; IntAct=EBI-4426649, EBI-4424123;
CC       Q17TI5; Q9LVG2: TOE2; NbExp=4; IntAct=EBI-4426649, EBI-4424568;
CC       Q17TI5; Q9SZG3: VQ29; NbExp=3; IntAct=EBI-4426649, EBI-25517843;
CC       Q17TI5; Q0WQX9: WAVH2; NbExp=3; IntAct=EBI-4426649, EBI-4426718;
CC       Q17TI5; Q93WY4: WRKY12; NbExp=3; IntAct=EBI-4426649, EBI-25513081;
CC       Q17TI5; Q9SJA8: WRKY17; NbExp=6; IntAct=EBI-4426649, EBI-2365037;
CC       Q17TI5; Q9CAR4: WRKY36; NbExp=3; IntAct=EBI-4426649, EBI-15210240;
CC       Q17TI5; Q9FQ04: XRN4; NbExp=3; IntAct=EBI-4426649, EBI-25511549;
CC   -!- SUBCELLULAR LOCATION: Nucleus. Cell membrane
CC       {ECO:0000269|PubMed:28652362}; Peripheral membrane protein; Cytoplasmic
CC       side. Note=The translocation to the nucleus depends on the auxin
CC       concentration. Polar localization at the plasma membrane, rootward
CC       oriented, in developing root protophloem cells (PubMed:28652362).
CC       {ECO:0000269|PubMed:28652362}.
CC   -!- TISSUE SPECIFICITY: Expressed in the developing protophloem up to the
CC       elongation zone in root meristem of young seedlings, in the columella
CC       and the phloem vasculature throughout the root and in the phloem
CC       vasculature in the shoot (PubMed:23569225). Detected in the shoot
CC       meristem and in primordia. Low expression in stomata. Confined to sieve
CC       element precursor cells and to protophloem (PubMed:25049386).
CC       {ECO:0000269|PubMed:17006513, ECO:0000269|PubMed:19201913,
CC       ECO:0000269|PubMed:20649916, ECO:0000269|PubMed:21149702,
CC       ECO:0000269|PubMed:23569225, ECO:0000269|PubMed:25049386}.
CC   -!- DEVELOPMENTAL STAGE: Ubiquitously expressed in early embryos and
CC       becomes restricted to the vasculature in the mature embryo and at later
CC       stages of development (PubMed:19465596). Expressed in roots developing
CC       protophloem, up to the end of the transition zone, as well as in the
CC       root tip meristem (PubMed:23569225). {ECO:0000269|PubMed:19465596,
CC       ECO:0000269|PubMed:23569225}.
CC   -!- INDUCTION: Up-regulated by auxin and down-regulated by brassinolide.
CC       {ECO:0000269|PubMed:17006513}.
CC   -!- DOMAIN: The DZC domain is necessary and sufficient for dimerization. A
CC       C-terminal fragment containing both DZC domains is able to rescue the
CC       short root phenotype. The N-terminal part (1-57) promotes BRX membrane
CC       association and is required for efficient degradation in the nucleus.
CC       {ECO:0000269|PubMed:16514016}.
CC   -!- DISRUPTION PHENOTYPE: Impaired primary root protophloem
CC       differentiation. Short primary root and increased number of lateral
CC       roots (PubMed:25049386, PubMed:28652362). Absent sieve element
CC       precursor division, occurrence of gap cells lacking actin filament,
CC       associated with a reduction in the number of early dividing protophloem
CC       cells, in root meristem size and root growth; these phenotypes are
CC       partially rescued in plants also missing MAKR5 (PubMed:25049386,
CC       PubMed:28652362, PubMed:27354416). Patchy expression of SUC2
CC       (PubMed:25049386). Reduced cotyledon and leaf size. Enhanced response
CC       to abscisic acid-mediated inhibition of root growth and insensitivity
CC       to cytokinin induced inhibition of lateral root initiation. The double
CC       mutant brx ops double mutant has strongly reduced root length and
CC       meristem size, with missing protophloem strands (PubMed:28652362). The
CC       disruption of BAM3 restores root protophloem and mersitem phenotypes
CC       observed in brx mutants (PubMed:23569225). Ectopic overexpression of
CC       BAM3 but slightly reduced CLE45 levels in root meristems
CC       (PubMed:23569225). {ECO:0000269|PubMed:19037657,
CC       ECO:0000269|PubMed:19201913, ECO:0000269|PubMed:20649916,
CC       ECO:0000269|PubMed:23569225, ECO:0000269|PubMed:25049386,
CC       ECO:0000269|PubMed:27354416, ECO:0000269|PubMed:28652362}.
CC   -!- MISCELLANEOUS: The truncated variant in cv. Uk-1 results in short root
CC       phenotype.
CC   -!- SIMILARITY: Belongs to the BRX family. {ECO:0000305}.
CC   -!- SEQUENCE CAUTION:
CC       Sequence=AAG50720.1; Type=Erroneous gene model prediction; Evidence={ECO:0000305};
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DR   EMBL; AY702648; ABG25052.1; -; mRNA.
DR   EMBL; AY702649; ABG25053.1; -; mRNA.
DR   EMBL; AC079041; AAG50720.1; ALT_SEQ; Genomic_DNA.
DR   EMBL; CP002684; AEE31412.1; -; Genomic_DNA.
DR   EMBL; BT002854; AAO22671.1; -; mRNA.
DR   EMBL; BT004390; AAO42384.1; -; mRNA.
DR   PIR; A86443; A86443.
DR   RefSeq; NP_174471.2; NM_102925.3.
DR   AlphaFoldDB; Q17TI5; -.
DR   SMR; Q17TI5; -.
DR   BioGRID; 25312; 96.
DR   IntAct; Q17TI5; 94.
DR   STRING; 3702.AT1G31880.1; -.
DR   PaxDb; Q17TI5; -.
DR   PRIDE; Q17TI5; -.
DR   ProteomicsDB; 240364; -.
DR   EnsemblPlants; AT1G31880.1; AT1G31880.1; AT1G31880.
DR   GeneID; 840078; -.
DR   Gramene; AT1G31880.1; AT1G31880.1; AT1G31880.
DR   KEGG; ath:AT1G31880; -.
DR   Araport; AT1G31880; -.
DR   TAIR; locus:2034486; AT1G31880.
DR   eggNOG; ENOG502QU4N; Eukaryota.
DR   HOGENOM; CLU_033380_0_1_1; -.
DR   InParanoid; Q17TI5; -.
DR   PhylomeDB; Q17TI5; -.
DR   PRO; PR:Q17TI5; -.
DR   Proteomes; UP000006548; Chromosome 1.
DR   ExpressionAtlas; Q17TI5; baseline and differential.
DR   Genevisible; Q17TI5; AT.
DR   GO; GO:0005634; C:nucleus; IDA:TAIR.
DR   GO; GO:0005886; C:plasma membrane; IEA:UniProtKB-SubCell.
DR   GO; GO:0042802; F:identical protein binding; IPI:TAIR.
DR   GO; GO:0010315; P:auxin export across the plasma membrane; IDA:TAIR.
DR   GO; GO:0009734; P:auxin-activated signaling pathway; IMP:TAIR.
DR   GO; GO:0030154; P:cell differentiation; IMP:UniProtKB.
DR   GO; GO:0009736; P:cytokinin-activated signaling pathway; IMP:TAIR.
DR   GO; GO:0048527; P:lateral root development; IMP:TAIR.
DR   GO; GO:0010078; P:maintenance of root meristem identity; IMP:UniProtKB.
DR   GO; GO:0010088; P:phloem development; IMP:UniProtKB.
DR   GO; GO:2000280; P:regulation of root development; IMP:UniProtKB.
DR   GO; GO:0009737; P:response to abscisic acid; IMP:TAIR.
DR   GO; GO:0048364; P:root development; IMP:TAIR.
DR   GO; GO:0048756; P:sieve cell differentiation; IMP:TAIR.
DR   InterPro; IPR013591; Brevis_radix_dom.
DR   InterPro; IPR044532; BRX-like.
DR   InterPro; IPR027988; BRX_N.
DR   PANTHER; PTHR46058; PTHR46058; 1.
DR   Pfam; PF08381; BRX; 2.
DR   Pfam; PF13713; BRX_N; 1.
DR   PROSITE; PS51514; BRX; 2.
PE   1: Evidence at protein level;
KW   Cell membrane; Developmental protein; Differentiation; Membrane; Nucleus;
KW   Reference proteome; Repeat.
FT   CHAIN           1..344
FT                   /note="Protein BREVIS RADIX"
FT                   /id="PRO_0000373821"
FT   DOMAIN          139..194
FT                   /note="BRX 1"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00847"
FT   DOMAIN          289..344
FT                   /note="BRX 2"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00847"
FT   REGION          203..286
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        214..234
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        267..286
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   VARIANT         141..344
FT                   /note="Missing (in strain: cv. Uk-1)"
FT   VARIANT         310
FT                   /note="T -> S (in strain: cv. Uk-2)"
SQ   SEQUENCE   344 AA;  38761 MW;  D36075D26158FFD7 CRC64;
     MFSCIACTKA DGGEEVEHGA RGGTTPNTKE AVKSLTIQIK DMALKFSGAY KQCKPCTGSS
     SSPLKKGHRS FPDYDNASEG VPYPFMGGSA GSTPAWDFTN SSHHPAGRLE SKFTSIYGND
     RESISAQSCD VVLDDDGPKE WMAQVEPGVH ITFASLPTGG NDLKRIRFSR EMFDKWQAQR
     WWGENYDKIV ELYNVQRFNR QALQTPARSD DQSQRDSTYS KMDSARESKD WTPRHNFRPP
     GSVPHHFYGG SSNYGPGSYH GGPPMDAART TTSSRDDPPS MSNASEMQAE WIEEDEPGVY
     ITIRQLSDGT RELRRVRFSR ERFGEVHAKT WWEQNRERIQ TQYL
 
 
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