全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
PLOS ONE  2012 

454 Transcriptome Sequencing Suggests a Role for Two-Component Signalling in Cellularization and Differentiation of Barley Endosperm Transfer Cells

DOI: 10.1371/journal.pone.0041867

Full-Text   Cite this paper   Add to My Lib

Abstract:

Background Cell specification and differentiation in the endosperm of cereals starts at the maternal-filial boundary and generates the endosperm transfer cells (ETCs). Besides the importance in assimilate transfer, ETCs are proposed to play an essential role in the regulation of endosperm differentiation by affecting development of proximate endosperm tissues. We attempted to identify signalling elements involved in early endosperm differentiation by using a combination of laser-assisted microdissection and 454 transcriptome sequencing. Principal Findings 454 sequencing of the differentiating ETC region from the syncytial state until functionality in transfer processes captured a high proportion of novel transcripts which are not available in existing barley EST databases. Intriguingly, the ETC-transcriptome showed a high abundance of elements of the two-component signalling (TCS) system suggesting an outstanding role in ETC differentiation. All components and subfamilies of the TCS, including distinct kinds of membrane-bound receptors, have been identified to be expressed in ETCs. The TCS system represents an ancient signal transduction system firstly discovered in bacteria and has previously been shown to be co-opted by eukaryotes, like fungi and plants, whereas in animals and humans this signalling route does not exist. Transcript profiling of TCS elements by qRT-PCR suggested pivotal roles for specific phosphorelays activated in a coordinated time flow during ETC cellularization and differentiation. ETC-specificity of transcriptionally activated TCS phosphorelays was assessed for early differentiation and cellularization contrasting to an extension of expression to other grain tissues at the beginning of ETC maturation. Features of candidate genes of distinct phosphorelays and transcriptional activation of genes putatively implicated in hormone signalling pathways hint at a crosstalk of hormonal influences, putatively ABA and ethylene, and TCS signalling. Significance Our findings suggest an integral function for the TCS in ETC differentiation possibly coupled to sequent hormonal regulation by ABA and ethylene.

References

[1]  Weber H, Borisjuk L, Wobus U (2005) Molecular physiology of legume seed development. Ann Rev Plant Biol 56: 253–279.
[2]  Olsen O-A (2001) Endosperm development: cellularization and cell fate specification. Ann Rev Plant Physiol Plant Mol Biol 52: 233–267.
[3]  Gruis D, Guo H, Selinger D (2006) Surface position, not signalling from surrounding maternal tissues, specifies aleurone epidermal cell fate in maize. Plant Physiol 141: 1771–1780.
[4]  Thiel J, Müller M, Weschke W, Weber H (2009) Amino acid metabolism at the maternal-filial boundary of young barley seeds: a microdissection-based study. Planta 230: 205–213.
[5]  Thiel J, Weier D, Sreenivasulu N, Strickert M, Weichert N, et al. (2008) Different hormonal regulation of cellular differentiation and function in nucellar projection and endosperm transfer cells –a microdissection-based transcriptome study of young barley grains. Plant Physiol 148: 1436–1452.
[6]  R?der MS, Kaiser C, Weschke W (2006) Molecular mapping of the shrunken endosperm genes seg8 and sex1 in barley (Hordeum vulgare L.). Genome 49: 1–6.
[7]  Sreenivasulu N, Radchuk V, Alawady A, Borisjuk L, Weier D, et al. (2010) De-regulation of abscisic acid contents causes abnormal endosperm development in the barley mutant seg8. Plant J 64: 589–603.
[8]  Emrich SJ, Barbazuk WB, Li L, Schnable PS (2007) Gene discovery and annotation using LCM-454 transcriptome sequencing. Genome Res 17: 69–73.
[9]  Mu?iz LM, Royo J, Gómez E, Barrero C, Bergareche D, et al. (2006) The maize transfer cell-specific type-A response regulator ZmTCRR-1 appears to be involved in intercellular signalling. Plant J 48: 17.
[10]  Mu?iz LM, Royo J, Gómez E, Baudot G, Paul W, et al. (2010) Atypical response regulators expressed in the maize endosperm transfer cells link canonical two component system and seed biology. BMC Plant Biol 10: 84.
[11]  Schaller GE, Kieber JJ, Shiu S-H (2008) Two-component signalling elements and histidyl-aspartyl phosphrelays. The Arabidopsis Book doi: 10.1199/tab.0112.
[12]  Schaller GE, Doi K, Hwang I, Kieber JJ, Khurana JP, et al. (2007) Nomenclature for two-component signaling elements of rice. Plant Physiol 143: 555–557.
[13]  Mayer K, Martis M, Hedley PE, Simkova H, Liu H, et al. (2011) Unlocking the barley genome by chromosomal and comparative genomics. Plant Cell 23: 1249–1263.
[14]  Tran LP, Urao T, Qin F, Maruyama K, Kakimoto T, et al. (2007) Functional analysis of AHK1/ATHK1 and cytokinin receptor histidine kinases in response to abscisic acid, drought, and salt stress in Arabidopsis. Proc Natl Acad Sci USA 104: 20623–20628.
[15]  Wohlbach DJ, Quirino BF, Sussman MR (2008) Analysis of the Arabidopsis histidine kinase ATHK1 reveals a connection between vegetative osmotic stress sensing and seed maturation. Plant Cell 20: 1101–1117.
[16]  Imamura A, Hanaki N, Nakamura A, Suzuki T, Taniguchi M, et al. (1999) Compilation and characterization of Arabidopsis thaliana response regulators implicated in His-Asp phosphorelay signal transduction. Plant Cell Physiol 40: 733–742.
[17]  Makino S, Kiba T, Imamura A, Hanaki N, Nakamura A, et al. (2000) Genes encoding pseudo-response regulators: insight into His-to-Asp phosphorelay and circadian rhythm in Arabidopsis thaliana. Plant Cell Physiol 41: 791–803.
[18]  Matas AJ, Yeats TH, Buda GJ, Zheng Y, Chatterjee S, et al. (2011) Tissue- and cell-type specific transcriptome profiling of expanding tomato fruit provides insights into metabolic and regulatory specialization and cuticle formation. Plant Cell 23: 3893–3910.
[19]  Torti S, Fornara F, Vincent C, Andrés F, Nordstr?m K, et al. (2012) Analysis of the Arabidopsis shoot meristem transcriptome during floral transition identifies distinct regulatory patterns and a leucine-rich repeat protein that promotes flowering. Plant Cell 24: 444–462.
[20]  Schmid MW, Schmidt A, Klostermeier UC, Barann M, Rosenstiel P, et al. (2012) A powerful method for transcriptional profiling of specific cell types in eukaryotes: laser-assisted microdissection and RNA sequencing. PLoS ONE 7: e29685.
[21]  Pischke MS, Jones LG, Otsuga D, Fernandez DE, Drews GN, et al. (2002) An Arabidopsis histidine kinase is essential for megagametogenesis. Proc Natl Acad Sci USA 99: 15800–15805.
[22]  Deng Y, Dong H, Mu J, Ren B, Zheng B, et al. (2010) Arabidopsis histidine kinase CKI1 acts upstream of histidine phosphotransfer proteins to regulate female gametophyte development and vegetative growth. Plant Cell 22: 1232–1248.
[23]  Hejatko J, Pernisova M, Eneva T, Palme K, Brzobohaty B (2003) The putative sensor histidine kinase CKI1 is involved in gametophyte development in Arabidopsis. Mol Genet Genomics 269: 443–453.
[24]  Hejatko J, Ryu H, Kim GT, Dobesova R, Choi S, et al. (2009) The histidine kinases Cytokinin-Independent1 and Arabidopsis Histidine Kinase2 and 3 regulate vascular tissue development in Arabidopsis shoots. Plant Cell 21: 2008–2021.
[25]  Zimmermann P, Hirsch-Hoffmann M, Henning L, Gruissem W (2004) Genevestigator. Arabidopsis microarray database and analysis toolbox. Plant Physiol 136: 2621–2632.
[26]  Boisnard-Lorig C, Colon-Carmona A, Bauch M, Hodge S, Doerner P, et al. (2001) YFP fusion protein in Arabidopsis show that syncytial endosperm is divided in mitotic domains. Plant Cell 13: 495–509.
[27]  Scott RJ, Spielman M, Bailey J, Dickinson HG (1998) Parent-of-origin effects on seed development in Arabidopsis thaliana. Development 125: 3329–3341.
[28]  Day RC, Herridge RP, Ambrose BA, Macknight RC (2008) Transcriptome analysis of proliferating Arabidopsis endosperm reveals biological implications for the control of syncytial division, cytokinin signaling, and gene expression regulation. Plant Physiol 148: 1964–1984.
[29]  Yang J, Zhang J, Wang Z, Liu K, Wand P (2006) Post-anthesis development of inferior and superior spikelets in rice in relation to abscisic acid and ethylene. J Exp Bot 57: 149–160.
[30]  Brandstatter I, Kieber JJ (1998) Two genes with similarity to bacterial response regulators are rapidly and specifically induced by cytokinin in Arabidopsis. Plant Cell 10: 1009–1019.
[31]  Kiba T, Yamada H, Sato S, Kato T, Tabata S, et al. (2003) The type-A response regulator, ARR15, acts as a negative regulator in the cytokinin-mediated signal transduction in Arabidopsis thaliana. Plant Cell Physiol 44: 868–874.
[32]  To JP, Haberer G, Ferreira FJ, Deruere J, Mason MG, et al. (2004) Type-A Arabidopsis response regulators are partially redundant negative regulators of cytokinin signaling. Plant Cell 16: 658–671.
[33]  To JP, Deruère J, Maxwell BB, Morris VF, Hutchison CE, et al. (2007) Cytokinin regulates type-A Arabidopsis Response Regulator activity and protein stability via two-component phosphorelay. Plant Cell 19: 3901–3914.
[34]  Sakai H, Aoyama T, Oka A (2000) Arabidopsis ARR1 and ARR2 response regulators operate as transcriptional activators. Plant J 24: 703–711.
[35]  Leibfried A, To JP, Busch W, Stehling S, Kehle A, et al. (2005) WUSCHEL controls meristem function by direct regulation of cytokinin-inducible response regulators. Nature 438: 1172–1175.
[36]  Chang WC, Lee TY, Huang HD, Huang HY, Pan RL (2008) PlantPAN: Plant promoter analysis navigator, for identifying combinatorial cis-regulatory elements with distance constraint in plant gene groups. BMC Genomics 26: 561.
[37]  Johannesson H, Wang Y, Hanson J, Engstr?m P (2003) The Arabidopsis thaliana homeobox gene ATHB5 is a potential regulator of abscisic acid responsiveness in developing seedlings. Plant Mol Biol 51: 719–729.
[38]  Niu X, Helentjaris T, Bate NJ (2002) Maize ABI4 binds coupling element1 in abscisic acid and sugar response genes. Plant Cell 14: 2565–2575.
[39]  Abe H, Urao T, Ito T, Seki M, Shinozaki K, et al. (2003) Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) function as transcriptional activators in abscisic acid signaling. Plant Cell 15: 63–78.
[40]  Zhang ZL, Xie Z, Zou X, Casaretto J, Ho TH, et al. (2004) A rice WRKY gene encodes a transcriptional repressor of the gibberellin signaling pathway in aleurone cells. Plant Physiol 134: 1500–1513.
[41]  Kagaya Y, Ohmiya K, Hattori T (1999) RAV1, a novel DNA-binding protein, binds to bipartite recognition sequence through two distinct DNA. Nucleic Acids Res 27: 470–478.
[42]  Shen Q, Chen CN, Brands A, Pan SM, Ho THD (2001) The stress- and abscisic acid induced barley gene HVA22: developmental regulation and homologues in diverse organisms. Plant Mol Biol 45: 327–340.
[43]  Tsai AY, Gazzarrini S (2012) AKIN10 and FUSCA3 interact to control lateral organ development and phase transitions in Arabidopsis. Plant J 69: 809–821.
[44]  Schaller GE, Bleecker AB (1995) Ethylene-binding sites generated in yeast expressing the Arabidopsis ETR1 gene. Science 270: 1807–1811.
[45]  Hall AE, Findell JL, Schaller GE, Sisler EC, Bleecker AB (2000) Ethylene perception by the ERS1 protein in Arabidopsis. Plant Physiol 123: 1449–1458.
[46]  Chen Y-F, Etheridge N, Schaller GE (2005) Ethylene signal transduction. Ann Bot 95: 901–915.
[47]  Rashotte AM, Mason MG, Hutchison CE, Ferreira FJ, Schaller GE, et al. (2006) A subset of Arabidopsis AP2 transcription factors mediates cytokinin responses in concert with a two-component pathway. Proc Natl Acad Sci USA 103: 11081–11085.
[48]  Yokoyama A, Yamashino T, Amano Y, Tajima Y, Imamura A, et al. (2007) Type-B ARR transcription factors, ARR10 and ARR12, are implicated in cytokinin-mediated regulation of protoxylem differentiation in roots of Arabidopsis thaliana. Plant Cell Physiol 48: 84–96.
[49]  Argyros RD, Mathews DE, Chiang YH, Palmer CM, Thibault DM, et al. (2008) Type B response regulators of Arabidopsis play key roles in cytokinin signaling and plant development. Plant Cell 20: 2102–2116.
[50]  Hass C, Lohrmann J, Albrect V, Sweere U, Hummel F, et al. (2004) The response regulator 2 mediates ethylene signaling and hormone signal integration in Arabidopsis. EMBO J 23: 3290–3302.
[51]  Mason MG, Mathews DE, Argyros DA, Maxwell BB, Kieber JJ, et al. (2005) Multiple type-B response regulators mediate cytokinin signal transduction in Arabidopsis. Plant Cell 17: 3007–3018.
[52]  Urao T, Miyata S, Yamaguchi-Shinozaki K, Shinozaki K (2000) Possible His to Asp phosphorelay signaling in an Arabidopsis two-component system. FEBS Lett 478: 227–232.
[53]  Weschke W, Panitz R, Sauer N, Wang Q, Neubohn B, et al. (2000) Sucrose transport into barley seeds: molecular characterization of two transporters and implications for seed development and starch accumulation. Plant J 21: 455–467.
[54]  Dibley SJ, Zhou Y, Adriunas FA, Talbot MJ, Offler CE, et al. (2009) Early gene expression programs accompanying trans-differentiation of epidermal cells of Vicia faba cotyledons into transfer cells. New Phytol 182: 863–877.
[55]  Schikora A, Schmidt W (2002) Formation of transfer cells and H(+)-ATPase expression in tomato roots under P and Fe deficiency. Planta 215: 304–311.
[56]  Thiel J, Riewe D, Rutten T, Melzer M, Friedel S, et al. (2012) Differentiation of endosperm transfer cells of barley - a comprehensive analysis at the micro-scale. Plant J doi: 10.1111/j.1365-313X.2012.05018.x.
[57]  Thiel J, Weier D, Weschke W (2011) Laser-capture microdissection of developing barley seeds and cDNA array analysis of selected tissues. Methods Mol Biol 755: 461–475.
[58]  Zhang Z, Schwartz S, Wagner L, Miller W (2000) A greedy algorithm for aligning DNA sequences. J Comput Biol 7: 203–214.
[59]  Huang X, Madan A (1999) CAP3: A DNA Sequence Assembly Program. Genome Research 9: 868–877.
[60]  Zdobnov EM, Apweiler R (2001) InterProScan -an integration platform for the signature-recognition methods in InterPro. Bioinformatics 17: 847–848.
[61]  Czechowski T, Stitt M, Altmann T, Udvardi MK, Scheible W-R (2004) Genome-wide identification and testing of superior reference genes for transcript normalization in Arabidopsis. Plant Physiol 139: 5–17.
[62]  Neuberger T, Srenivasulu N, Rokitta M, Rolletschek H, G?bel C, et al. (2008) Quantitative imaging of oil storage in developing crop seeds. Plant Biotech J 6: 31–45.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133