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Formin homology 1 (OsFH1) regulates root-hair elongation in rice (Oryza sativa)

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Abstract

The outgrowth of root hairs from the epidermal cell layer is regulated by a strict genetic regulatory system and external growth conditions. Rice plants cultivated in water-logged paddy land are exposed to a soil ecology that differs from the environment surrounding upland plants, such as Arabidopsis and maize. To identify genes that play important roles in root-hair growth, a forward genetics approach was used to screen for short-root-hair mutants. A short-root-hair mutant was identified, and the gene was isolated using map-based cloning and sequencing. The mutant harbored a point mutation at a splicing acceptor site, which led to truncation of OsFH1 (rice formin homology 1). Subsequent analysis of two additional T-DNA mutants verified that OsFH1 is important for root-hair elongation. Further studies revealed that the action of OsFH1 on root-hair growth is dependent on growth conditions. The mutant Osfh1 exhibited root-hair defects when roots were grown submerged in solution, and mutant roots produced normal root hairs in the air. However, root-hair phenotypes of mutants were not influenced by the external supply of hormones or carbohydrates, a deficiency of nutrients, such as Fe or P i , or aeration. This study shows that OsFH1 plays a significant role in root-hair elongation in a growth condition-dependent manner.

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Abbreviations

2,4-D:

2,4-Dichlorophenoxyacetic acid

ACC:

1-Aminocyclopropane-1-carboxylic acid

Ac/Ds:

Activator/dissociation

Bnip:

BUD NECK INVOLVED PROTEIN

CPC:

CAPRICE

Cryo-SEM:

Cryo-scanning electron microscope

FH1:

Formin homology 1

GL2:

GLABRA 2

LRR:

Leucine-rich repeat

NAA:

Naphthalene-1-acetic acid

PAC:

P1-based artificial chromosome

PI:

Propidium iodine

PRR:

Proline-rich region

qRT-PCR:

Quantitative reverse transcriptase PCR

sGFP:

Synthetic green fluorescent protein

References

  • Bailey-Serres J, Voesenek LA (2008) Flooding stress: acclimations and genetic diversity. Annu Rev Plant Biol 59:313–339. doi:10.1146/annurev.arplant.59.032607.092752

    Article  PubMed  CAS  Google Scholar 

  • Baxter-Burrell A, Yang Z, Springer PS, Bailey-Serres J (2002) RopGAP4-dependent Rop GTPase rheostat control of Arabidopsis oxygen deprivation tolerance. Science 296(5575):2026–2028. doi:10.1126/science.1071505

    Article  PubMed  CAS  Google Scholar 

  • Blanchoin L, Staiger CJ (2010) Plant formins: diverse isoforms and unique molecular mechanism. Biochim Biophys Acta 1803(2):201–206. doi:10.1016/j.bbamcr.2008.09.015

    Article  PubMed  CAS  Google Scholar 

  • Carol RJ, Takeda S, Linstead P, Durrant MC, Kakesova H, Derbyshire P, Drea S, Zarsky V, Dolan L (2005) A RhoGDP dissociation inhibitor spatially regulates growth in root hair cells. Nature 438(7070):1013–1016. doi:10.1038/nature04198

    Article  PubMed  CAS  Google Scholar 

  • Cernac A, Lincoln C, Lammer D, Estelle M (1997) The SAR1 gene of Arabidopsis acts downstream of the AXR1 gene in auxin response. Development 124(8):1583–1591

    PubMed  CAS  Google Scholar 

  • Cheung AY, Wu HM (2004) Overexpression of an Arabidopsis formin stimulates supernumerary actin cable formation from pollen tube cell membrane. Plant Cell 16(1):257–269. doi:10.1105/tpc.016550

    Article  PubMed  CAS  Google Scholar 

  • Cho HT, Cosgrove DJ (2002) Regulation of root hair initiation and expansin gene expression in Arabidopsis. Plant Cell 14(12):3237–3253

    Article  PubMed  CAS  Google Scholar 

  • Colmer TD, Voesenek LA (2009) Flooding tolerance: suites of plant traits in variable environments. Funct Plant Biol 36(8):665–681. doi:10.1071/FP09144

    Google Scholar 

  • Cvrckova F, Novotny M, Pickova D, Zarsky V (2004) Formin homology 2 domains occur in multiple contexts in angiosperms. BMC Genomics 5(1):44. doi:10.1186/1471-2164-5-44

    Article  PubMed  Google Scholar 

  • Deeks MJ, Cvrckova F, Machesky LM, Mikitova V, Ketelaar T, Zarsky V, Davies B, Hussey PJ (2005) Arabidopsis group Ie formins localize to specific cell membrane domains, interact with actin-binding proteins and cause defects in cell expansion upon aberrant expression. New Phytol 168(3):529–540. doi:10.1111/j.1469-8137.2005.01582.x

    Article  PubMed  CAS  Google Scholar 

  • Deeks MJ, Fendrych M, Smertenko A, Bell KS, Oparka K, Cvrckova F, Zarsky V, Hussey PJ (2010) The plant formin AtFH4 interacts with both actin and microtubules, and contains a newly identified microtubule-binding domain. J Cell Sci 123(Pt 8):1209–1215. doi:10.1242/jcs.065557

    Article  PubMed  CAS  Google Scholar 

  • Ding W, Yu Z, Tong Y, Huang W, Chen H, Wu P (2009) A transcription factor with a bHLH domain regulates root hair development in rice. Cell Res 19(11):1309–1311. doi:10.1038/cr.2009.109

    Article  PubMed  Google Scholar 

  • Dolan L, Janmaat K, Willemsen V, Linstead P, Poethig S, Roberts K, Scheres B (1993) Cellular organisation of the Arabidopsis thaliana root. Development 119(1):71–84

    PubMed  CAS  Google Scholar 

  • Favery B, Chelysheva LA, Lebris M, Jammes F, Marmagne A, De Almeida-Engler J, Lecomte P, Vaury C, Arkowitz RA, Abad P (2004) Arabidopsis forminAtFH6 is a plasma membrane-associated protein upregulated in giant cells induced by parasitic nematodes. Plant Cell 16(9):2529–2540. doi:10.1105/tpc.104.024372

    Article  PubMed  CAS  Google Scholar 

  • Fitz Gerald JN, Hui PS, Berger F (2009) Polycomb group-dependent imprinting of the actin regulator AtFH5 regulates morphogenesis in Arabidopsis thaliana. Development 136(20):3399–3404. doi:10.1242/dev.036921

    Article  PubMed  CAS  Google Scholar 

  • Galway ME, Masucci JD, Lloyd AM, Walbot V, Davis RW, Schiefelbein JW (1994) The TTG gene is required to specify epidermal cell fate and cell patterning in the Arabidopsis root. Dev Biol 166(2):740–754. doi:10.1006/dbio.1994.1352

    Article  PubMed  CAS  Google Scholar 

  • Galway ME, Heckman JW Jr, Schiefelbein JW (1997) Growth and ultrastructure of Arabidopsis root hairs: the rhd3 mutation alters vacuole enlargement and tip growth. Planta 201(2):209–218

    Article  PubMed  CAS  Google Scholar 

  • Grebe M (2012) The patterning of epidermal hairs in Arabidopsis-updated. CurrOpin Plant Biol 15(1):31–37. doi:10.1016/j.pbi.2011.10.010

    Article  CAS  Google Scholar 

  • Grunt M, Zarsky V, Cvrckova F (2008) Roots of angiosperm formins: the evolutionary history of plant FH2 domain-containing proteins. BMC Evol Biol 8:115. doi:10.1186/1471-2148-8-115

    Article  PubMed  Google Scholar 

  • Hermans C, Porco S, Vandenbussche F, Gille S, De Pessemier J, Van Der Straeten D, Verbruggen N, Bush DR (2011) Dissecting the role of CHITINASE-LIKE1 in nitrate-dependent changes in root architecture. Plant Physiol 157(3):1313–1326. doi:10.1104/pp.111.181461

    Article  PubMed  CAS  Google Scholar 

  • Holbrook NM, Zwieniecki MA (2003) Plant biology: water gate. Nature 425(6956):361. doi:10.1038/425361a

    Article  PubMed  CAS  Google Scholar 

  • Kim CM, Dolan L (2011) Root hair development involves asymmetric cell division in Brachypodium distachyon and symmetric division in Oryza sativa. New Phytol 192(3):601–610. doi:10.1111/j.1469-8137.2011.03839.x

    Article  PubMed  CAS  Google Scholar 

  • Kim CM, Piao HL, Park SJ, Chon NS, Je BI, Sun B, Park SH, Park JY, Lee EJ, Kim MJ, Chung WS, Lee KH, Lee YS, Lee JJ, Won YJ, Yi G, Nam MH, Cha YS, Yun DW, Eun MY, Han CD (2004) Rapid, large-scale generation of Ds transposant lines and analysis of the Ds insertion sites in rice. Plant J 39(2):252–263. doi:10.1111/j.1365-313X.2004.02116.x

    Article  PubMed  CAS  Google Scholar 

  • Kim CM, Park SH, Je BI, Park SH, Park SJ, Piao HL, Eun MY, Dolan L, Han CD (2007) OsCSLD1, a cellulose synthase-like D1 gene, is required for root hair morphogenesis in rice. Plant Physiol 143(3):1220–1230. doi:10.1104/pp.106.091546

    Article  PubMed  CAS  Google Scholar 

  • Li Y, Shen Y, Cai C, Zhong C, Zhu L, Yuan M, Ren H (2010) The type II Arabidopsis formin14 interacts with microtubules and microfilaments to regulate cell division. Plant Cell 22(8):2710–2726. doi:10.1105/tpc.110.075507

    Article  PubMed  CAS  Google Scholar 

  • Libault M, Brechenmacher L, Cheng J, Xu D, Stacey G (2010) Root hair systems biology. Trends Plant Sci 15(11):641–650. doi:10.1016/j.tplants.2010.08.010

    Article  PubMed  CAS  Google Scholar 

  • Ma JF, Goto S, Tamai K, Ichii M (2001) Role of root hairs and lateral roots in silicon uptake by rice. Plant Physiol 127(4):1773–1780

    Article  PubMed  CAS  Google Scholar 

  • Masucci JD, Schiefelbein JW (1994) Therhd6 Mutation of Arabidopsis thaliana Alters Root-Hair Initiation through an Auxin- and ethylene-associated process. Plant Physiol 106(4):1335–1346

    PubMed  CAS  Google Scholar 

  • Masucci JD, Schiefelbein JW (1996) Hormones act downstream of TTG and GL2 to promote root hair outgrowth during epidermis development in the Arabidopsis root. Plant Cell 8(9):1505–1517. doi:10.1105/tpc.8.9.1505

    PubMed  CAS  Google Scholar 

  • Miki T, Okawa K, Sekimoto T, Yoneda Y, Watanabe S, Ishizaki T, Narumiya S (2009) mDia2 shuttles between the nucleus and the cytoplasm through the importin-(Alb et al.)/(Abercrombie et al.)- and CRM1-mediated nuclear transport mechanism. J BiolChem 284(9):5753–5762. doi:10.1074/jbc.M806191200

    CAS  Google Scholar 

  • Muller M, Schmidt W (2004) Environmentally induced plasticity of root hair development in Arabidopsis. Plant Physiol 134(1):409–419. doi:10.1104/pp.103.029066

    Article  PubMed  Google Scholar 

  • Narukawa M, Watanabe K, Inoue Y (2010) Light-induced root hair formation in lettuce (Lactuca sativa L. cv. Grand Rapids) roots at low pH is brought by chlorogenic acid synthesis and sugar. J Plant Res 123(6):789–799. doi:10.1007/s10265-010-0328-3

    Article  PubMed  Google Scholar 

  • Paul AS, Pollard TD (2009) Review of the mechanism of processive actin filament elongation by formins. Cell Motil Cytoskelet 66(8):606–617. doi:10.1002/cm.20379

    Article  CAS  Google Scholar 

  • Pitts RJ, Cernac A, Estelle M (1998) Auxin and ethylene promote root hair elongation in Arabidopsis. Plant J 16(5):553–560

    Article  PubMed  CAS  Google Scholar 

  • Pratley JN, Rosene HF (1954) Reversible azide inhibition of water influx into individual radish root-hair cells. J Cell Physiol 44(2):165–175

    Article  PubMed  CAS  Google Scholar 

  • Rosene HF, Bartlett LE (1950) Effect of anoxia on water influx of individual radish root hair cells. J Cell Physiol 36(1):83–96

    Article  PubMed  CAS  Google Scholar 

  • Shimmen T, Yokota E (2004) Cytplasmic streaming in plants. CurrOpin Cell Biol 16(1):68–72. doi:10.1016/j.ceb.2003.11.009

    Article  CAS  Google Scholar 

  • Sparkes IA, Runions J, Kearns A, Hawes C (2006) Rapid, transient expression of fluorescent fusion proteins in tobacco plants and generation of stably transformed plants. Nat Protoc 1(4):2019–2025. doi:10.1038/nprot.2006.286

    Article  PubMed  CAS  Google Scholar 

  • Toki S, Hara N, Ono K, Onodera H, Tagiri A, Oka S, Tanaka H (2006) Early infection of scutellum tissue with Agrobacterium allows high-speed transformation of rice. Plant J 47(6):969–976. doi:10.1111/j.1365-313X.2006.02836.x

    Article  PubMed  CAS  Google Scholar 

  • Tournaire-Roux C, Sutka M, Javot H, Gout E, Gerbeau P, Luu DT, Bligny R, Maurel C (2003) Cytosolic pH regulates root water transport during anoxic stress through gating of aquaporins. Nature 425(6956):393–397. doi:10.1038/nature01853

    Article  PubMed  CAS  Google Scholar 

  • Wymer CL, Bibikova TN, Gilroy S (1997) Cytoplasmic free calcium distributions during the development of root hairs of Arabidopsis thaliana. Plant J 12(2):427–439

    Article  PubMed  CAS  Google Scholar 

  • Xue XH, Guo CQ, Du F, Lu QL, Zhang CM, Ren HY (2011) AtFH8 is involved in root development under effect of low-dose latrunculin B in dividing cells. Mol Plant 4(2):264–278. doi:10.1093/mp/ssq085

    Article  PubMed  CAS  Google Scholar 

  • Yang W, Ren S, Zhang X, Gao M, Ye S, Qi Y, Zheng Y, Wang J, Zeng L, Li Q, Huang S, He Z (2011) BENT UPPERMOST INTERNODE1 encodes the class II formin FH5 crucial for actin organization and rice development. Plant Cell 23(2):661–680. doi:10.1105/tpc.110.081802

    Article  PubMed  CAS  Google Scholar 

  • Yi K, Guo C, Chen D, Zhao B, Yang B, Ren H (2005) Cloning and functional characterization of a formin-like protein (AtFH8) from Arabidopsis. Plant Physiol 138(2):1071–1082. doi:10.1104/pp.104.055665

    Article  PubMed  CAS  Google Scholar 

  • Young KG, Thurston SF, Copeland S, Smallwood C, Copeland JW (2008) INF1 is a novel microtubule-associated formin. Mol Biol Cell 19(12):5168–5180. doi:10.1091/mbc.E08-05-0469

    Article  PubMed  CAS  Google Scholar 

  • Yuo T (2009) Molecular cloning of a root hairless gene. Breed Sci 59:13–20

    Article  CAS  Google Scholar 

  • Zhang Z, Zhang Y, Tan H, Wang Y, Li G, Liang W, Yuan Z, Hu J, Ren H, Zhang D (2011) RICE MORPHOLOGY DETERMINANT encodes the type II formin FH5 and regulates rice morphogenesis. Plant Cell 23(2):681–700. doi:10.1105/tpc.110.081349

    Article  PubMed  Google Scholar 

  • ZhiMing Y, Bo K, XiaoWei H, ShaoLei L, YouHuang B, WoNa D, Ming C, Hyung-Taeg C, Ping W (2011) Root hair-specific expansins modulate root hair elongation in rice. Plant J 66(5):725–734. doi:10.1111/j.1365-313X.2011.04533.x

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

This work was supported by grants from the Next-Generation BioGreen 21 Program (PJ008215 and PJ008168), the Rural Development Administration, Republic of Korea. Jingmiao Liu is supported by a scholarship from the BK21 program. This research was also supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2011-0009096). We are grateful to Dr. Liam Dolan (University of Oxford, UK) for helping us with cryo-SEM work.

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Correspondence to Chang-deok Han.

Electronic supplementary material

Below is the link to the electronic supplementary material.

425_2013_1838_MOESM1_ESM.pdf

Online Resource 1 Primer sets used for map-based cloning. Primer sets such as S01054, R1M30, R1M471, RM6696, and RM1988 were obtained from public databases. The other primer sets were newly designed based on public rice sequence databases

425_2013_1838_MOESM2_ESM.pdf

Online Resource 2 Diagram of OsFH1 protein (a) and qRT-PCR analysis of truncated OsFH1 mRNA (b). The C-terminal truncations of Osfh1-2 and Osfh1-3 following insertion of T-DNA are shown by vertical arrows above the OsFH1 protein. The expression levels of truncated Osfh1-2 and Osfh1-3 were measured by qRT-PCR using the primer set denoted by horizontal arrows. Gene expression was normalized against the level of ubiquitin cDNA in the same samples. Error Bars represent standard deviations

425_2013_1838_MOESM3_ESM.pdf

Online Resource 3 Root-hair phenotype (a) and FH1ΔFH2 mRNA expression levels (b) of pUBI:FH1ΔFH2 transgenic plants. Four independent transgenic lines (pUBI:FH1ΔFH2) were generated in which amino acids 1–497 of OsFH1 (shown in ‘a’ of Online Resource 2) were expressed under the control of a ubiquitin promoter. The root-hair phenotypes of these four transgenic plant lines and that of the parental line Dongjin (DJ) were imaged by stereomicroscopy (upper panels). Bar, 500 μm. The root-hair lengths of these plants were measured (lower panels). b The expression levels of FH1ΔFH2 mRNA were measured by qRT-PCR. Gene expression was normalized against the level of ubiquitin cDNA in the same samples. Error Bars represent standard deviations

425_2013_1838_MOESM4_ESM.pdf

Online Resource 4 OsFH1 protein sequence, domain structure, and phylogenetic analysis with selected Arabidopsis and rice formins. a Protein sequence of OsFH1 analyzed using SMART and SignalP. Signal peptide (SP), proline-rich region (PRR), transmembrane domain (TMD), formin homology 1 (FH1) domain, and formin homology 2 (FH2) domain were shaded with different colors. Proline residues in PRR and FH1 domains, which are important for domain functions, were underlined in red. b Phylogenetic analysis of OsFH1 with selected Arabidopsis and rice formins. Protein sequences such as Bni1p (yeast), AtFH1, AtFH3, AtFH5, AtFH8, OsFH1, and OsFH5 were aligned. Two highly conserved motifs, which are important for formin functions, were marked with red and green colors, respectively

425_2013_1838_MOESM5_ESM.pdf

Online Resource 5 Comparison of the root-hair initiation zones of wild-type and Osfh1 mutant roots. a Seminal roots of 3-day-old plants were imaged by stereomicroscopy. Arrows indicate root-hair initiation sites. Bar, 500 μm. b Higher magnification views of arrowed regions are shown. Bar, 50 μm

425_2013_1838_MOESM6_ESM.pdf

Online Resource 6 Growth condition-dependent root-hair phenotypes of Osfh1. Germinating seeds of three mutants and their wild-type siblings were grown in three different conditions. In the first condition, plants were cultured on 1/2 MS soaked paper towels for 3 days (3 d Air). In the second condition, plants were cultured in 1/2 MS solution for 3 days (3 d Solution). In the third condition, plants were cultured in 1/2 MS for 1.5 days (1.5 d Solution) and then cultured on 1/2 MS soaked paper towels for an additional 1.5 days (1.5 d Solution + 1.5 d Air). After 3 days cultures, root hairs around 0.5-0.8 cm from the tips of seminal roots were photographed under the microscope. Bar, 500 μm

425_2013_1838_MOESM7_ESM.pdf

Online Resource 7 Effects of auxin and ACC on root-hair growth of Osfh1 mutants. Root hairs of Osfh1-1 and its wild-type siblings, which were cultured in 1/2 MS for 3 days and then moved to 1/2 MS supplemented with NAA (5 or 50 μM) or ACC (50, or 100 μM) for an additional 2 days, were inspected under the stereo-microscope. Bars, 500 μm

425_2013_1838_MOESM8_ESM.pdf

Online Resource 8 Effects of nutrients on short-root-hair phenotypes of Osfh1 mutants. Root hairs of OsFH1 and Osfh1 plants, which were cultured in Kimura B solution (one without KH2PO4 [Kimura B (–P)], and one without Fe-EDTA [Kimura B (-Fe)]) for 5 days, were inspected under the stereo-microscope. Bar, 500 μm

425_2013_1838_MOESM9_ESM.pdf

Online Resource 9 Gene expression pattern of OsFH1 analyzed using the rice array database (www.ricearray.org). Gene expression pattern of OsFH1 in whole plants, callus, suspension cell, dry seeds, germinating seeds, shoots, leaves, stems, whole internodes, roots, shoot apical meristems (SAM), flag leaves, ovaries, developing anthers, mature anthers, embryo sacs, embryos, and endosperm were examined using the rice Affymetrix expression database. The expression data were converted into the graph

425_2013_1838_MOESM10_ESM.pdf

Online Resource 10 Effects of aeration on root-hair growth of Osfh1 mutants. Osfh1-1, Osfh1-2 and Osfh1-3 mutants (Mut) and their corresponding wild-type siblings (WT) were cultured in 1/2 MS for 5 days without (a) or with (b) continuous aeration. Root hairs were imaged by stereomicroscopy. Error Bars represent standard deviations. **P < 0.01, Student’s t-test, n = 50. Bars, 500 μm

425_2013_1838_MOESM11_ESM.pdf

Online Resource 11 Effects of sucrose, glucose, and mannose on the root-hair growth of Osfh1 mutants. Wild-type and mutant plants were cultured for 5 days in 1/2 MS solution media (pH 4) supplemented with 50 mM (a) or 100 mM (b) sucrose, glucose or mannitol, and root-hair lengths were measured (c and d). Error Bars represent standard deviations. *P < 0.05, **P < 0.01, Student’s t-test, n = 50. Bars, 500 μm

425_2013_1838_MOESM12_ESM.pdf

Online Resource 12 Short statures of Osfh1-1, Osfh1-2, and Osfh1-3 mutant plants. a Wild-type (WT) and mutant plants of 5-day-old seedlings of Osfh1-1, Osfh1-2, and Osfh1-3. b Shoot length measurements of 5-day-old WT and mutant (Mutant) plants of Osfh1-1, Osfh1-2, and Osfh1-3. c Sixty-five-day-old WT and mutant plants grown in the field. Error Bars represent standard deviations. *P < 0.05, **P < 0.01, Student’s t test, n = 50. Bar, 10 cm (PDF 98 kb)

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Huang, J., Kim, C.M., Xuan, Yh. et al. Formin homology 1 (OsFH1) regulates root-hair elongation in rice (Oryza sativa). Planta 237, 1227–1239 (2013). https://doi.org/10.1007/s00425-013-1838-8

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