Tracheophyta > Magnoliopsida > Myrtales > Combretaceae > Lumnitzera > Lumnitzera littorea (Jack) Voigt. (2018). Supplementary Figure 6 | DEGs in different column development stages between L-1 and L-2. Plant Sci. Biotechnol. Int. Three biological replicates were prepared for sequencing. In the “biological process” category (34,918 unigenes), macromolecule metabolic process (4,389) was the largest subcategory. Ecol. Articles, Zunyi Vocational and Technical College, China, College of Resources and Environment, Qingdao Agricultural University, China. L. racemosa lives in the western part of its range, while L. littorea dominates the eastern part. 14, 433–438. Files are available under licenses specified on their description page. Interpreting Wetland Status. The protection of this species is facing a great challenge and the mangrove L. littorea is therefore is listed as a plant under state protection (category II) (Zhong et al., 2011; Zhang et al., 2013). Morphological observation showed that some flowers have a column embedded in the petals while others produce a stretched flower style during petal unfolding in flowering. However, little is known about the genomic regulation of flower development in L. littorea. Pyrrhanthus littoreus Jack Homonyms Lumnitzera littorea Voigt Common names Barat-barat in Malay … LliMADS1 and LliMADS9 belong to the B class of the AP3 subfamily, and LliMADS10 belongs to the SEP subfamily. In addition, geitonogamous selfing is not prevented within or between inflorescences on a plant when flowers are at different sexual phases in L. littorea (Zhang and Wolfe, 2016; Zhang et al., 2017). Petaloma alba Blanco. ; Teruntum merah (Lumnitzera littorea) Ng, Peter K. L. & N. Sivasothi, 1999.A Guide to the Mangroves of Singapore I (Plant Diversity). Biol. Lumnitzera littorea : Source: Melastomataceae+Lythraceae+Combretaceae of North America Update, database (version 2011) Acquired: 2011 : Notes: Updated for ITIS by the Flora of North America Expertise Network, in connection with an update for USDA PLANTS (2007-2010) Reference for: Lumnitzera littorea : Source: The PLANTS … These TFs were classed into 54 categories with bHLH, B3, bZIP, MYB-related, NAC, C2H2, C3H, ERF, WRKY, and MYB being the most highly represented (Figure 2A). doi: 10.1371/journal.pone.0123474, Hui, W.-K., Wang, Y., Chen, X.-Y., Zayed, M. Z., and Wu, G.-J. A de novo floral transcriptome reveals clues into Phalaenopsis orchid flower development. The outer circle shows the identified subfamily in MADS proteins. After PCR amplification for 15 cycles, the products were loaded onto flow cell channels at 12 pM for paired-end 150 bp × 2 sequencing with the Illumina HiSeq 4000 platform (Majorbio, Shanghai, China). The top five pathways were “carbon metabolism” (ko01200), “ribosome” (ko03010), “protein processing in endoplasmic reticulum” (ko04141), “biosynthesis of amino acids” (ko01230) and “oxidative phosphorylation” (ko00190) (Supplementary Figure S5). 35, 38–42. Identification of a MADS-box gene, FLOWERING LOCUS M, that represses flowering. Methods 25, 402–408. (2017). Most of the L. littorea flowers can only be pollinated from the same tree or even from the same flower (Li et al., 2016; Zhang et al., 2016, 2017). Teruntum merah … Lumnitzera littorea… 82,834 and 34,997 unigenes were assigned to 52 gene ontology (GO) functional groups and 364 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, respectively. Received: 18 July 2020; Accepted: 09 November 2020;Published: 08 December 2020. Chin. Validation of assembled unigenes by qPCR. Chen, Z., Rao, P., Yang, X., Su, X., Zhao, T., Gao, K., et al. Value Class Food As a result, 138,857 transcripts and 82,833 unigenes were annotated (Supplementary Figure S1). Plant J. Voigt) by artificial pollination. Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. Plant Cell 15, 2603–2611. Useful Tropical Plants Database 2014 by In the “cell component” (31,040 unigenes) and “molecular function” (16,876 unigenes) categories, intracellular (4,429) and nucleotide binding (2,755) were the most abundant GO terms, respectively. The morphology and evolution of L. littorea flowers have received substantial attention for their crucial reproductive functions. No use, distribution or reproduction is permitted which does not comply with these terms. After synthesis of the first-strand cDNA, the second-strand cDNA was produced using buffer, dNTPs, RNase H, and DNA polymerase I. 0. A total of 138,857 transcripts with a GC percent of 38.91%, average length of 1665.35 and an N50 size of 3049, were obtained (Table 1). doi: 10.1093/jxb/ert385, Yun, H., Hyun, Y., Kang, M. J., Noh, Y. S., Noh, B., and Choi, Y. The expression of 10 genes were down regulated and that of 7 genes were up regulated (Supplementary Table S6), consistent with those of the RNA-Seq data (Figure 3). However, little is known about the genomic regulation of flower development in L. littorea. UBIQUITIN-SPECIFIC PROTEASE 26 is required for seed development and the repression of PHERES1 in Arabidopsis. Biol. All transcripts and unigenes produced were searched against the NCBI NR, SwissProt, String, KEGG and Pfam databases with an E-value threshold < 1e–5. Soc. doi: 10.1093/molbev/msy096, Li, D., Liu, C., Shen, L., Wu, Y., Chen, H., Robertson, M., et al. PhytoImages.siu.edu image, phylogeny, nomenclature for Lumnitzera littorea. Plant Cell 15, 1538–1551. If you have any useful information about this plant, please leave a comment. Stamens are prominently exserted at anthesis after the stamens unfold. The double-strand cDNA was purified using the QIAquick PCR extraction kit (QIAGEN, Germany) and washed with EB buffer for end repair and single nucleotide adenine (A) addition. The SEP4 gene of Arabidopsis thaliana functions in floral organ and meristem identity. 26, 229–236. AoB Plants 10:ly051. Manag. doi: 10.1016/j.devcel.2008.05.002, Li, W., Zhang, L., Ding, Z., Wang, G., Zhang, Y., Gong, H., et al. (2014). Front. The GO annotation analysis classified groups of genes with significantly differential expression into three categories: the biological process, cellular component and molecular function categories (Supplementary Figure S6). Front. It is noted that the MADS, bZIP, bHLH, and MYB genes play key roles in the regulation of flower development and flowering time (Streisfeld et al., 2013; Wang et al., 2013; Rocheta et al., 2014). (2016). doi: 10.1038/353031a0, Ditta, G., Pinyopich, A., Robles, P., Pelaz, S., and Yanofsky, M. F. (2004). The similarity distribution analysis identified 41,687 transcripts and 13,958 unigenes that exhibited high sequence similarity (from 80% to 100%) with known gene sequences. The war of the whorls: genetic interactions controlling flower development. 30 doi: 10.1002/ece3.2827, Scortecci, K. C., Michaels, S. D., and Amasino, R. M. (2001). Alignments with E-values less than 1e–5 were chosen. Molecular and phylogenetic analyses of the complete MADS-box transcription factor family in Arabidopsis: new openings to the MADS world. Forest Resour. A total of 4,267 differentially expressed genes (DEGs), including 1,794 transcription factors (TFs), were identified between two types of flowers. Ecol. The unrooted phylogenetic tree was created with MEGA-X by the neighbor-joining method, and the bootstrap test was performed with 1,000 iterations. YZa and CZ designed the study and modified the manuscript. Here, we conducted de novo transcriptome sequencing of two kinds of flowering behavior with different types of style development for L. littorea in order to investigate gene expression patterns associated with special style development morphology. (2018). Using the stringent criteria of both FDR < 0.05 and |log2FC| > = 1, we detected 4,267 unigenes that were significantly different between L-1 and L-2. doi: 10.3724/SP.J.1145.2016.03021, Zhang, Y., Zhong, C., Li, S., Yan, T., and Guan, W. (2013). (2016). ID 49437 Symbol Key LULI8 Common Name N/A Family Combretaceae Category Dicot Division Magnoliophyta US Nativity Cultivated, or not in the U.S. US/NA Plant Yes State Distribution N/A Growth Habit N/A Plant J. Figure 2. In China, it is an endangered species confined to restricted regions of … Anders, S., and Huber, W. (2010). The different expression of these TFs indicated their possible different roles in modulating the formation of herkogamy flowers in L. littorea. Semin. : You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were … 16:31. doi: 10.1186/s13059-015-0597-1, Mertens, A., Brys, R., Schouppe, D., and Jacquemyn, H. (2018). The GO analysis indicated that a high number of unigenes were associated with the various biological processes and molecular functions in L. littorea floral tissues. Development 143, 3259–3271. Z., Lin, C. P., Cheng, T. C., Chang, B. C., Cheng, S. Y., Chen, Y.-W., et al. The structure of flowers in Lumnitzera littorea. A continuación se brinda un listado de las especies del género Lumnitzera aceptadas hasta julio de 2011, ordenadas alfabéticamente. (B) Phylogenetic relationships of MADS-box TF CDSs from L. littorea, Arabidopsis, Fragaria ananassa, and Hevea brasiliensis. Evol. Genome Biol. If you would like to support this site, please consider, http://ecocrop.fao.org/ecocrop/srv/en/home, Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. (2008). The SOC1 MADS-box gene integrates vernalization and gibberellin signals for flowering in Arabidopsis. LliMADS12 and AthPHERES1 (PHE1) are on the same branch in the Mγ subdivision of type I MADS-box genes. To identify the TFs represented in the L. littorea transcriptomes, all DEGs were searched against the plant TF database PlantTFDB 4.0 (Jin et al., 2014)7. doi: 10.1371/journal.pone.0010095, Rocheta, M., Sobral, R., Magalhaes, J., Amorim, M. I., Ribeiro, T., Pinheiro, M., et al. Sci. Nucleic Acids Res. To obtain an overview of the transcriptome profiles, L-1 and L-2 were sampled at different column development stages for Illumina deep sequencing. Richard Morris. doi: 10.1111/j.1365-313X.2006.02800.x, Grabherr, M. G., Haas, B. J., Yassour, M., Levin, J. The editor and reviewers' affiliations are the latest provided on their Loop research profiles and may not reflect their situation at the time of review. 45, 89–115. Tropicos.org 2019. International Plant Names Index. Lumnitzera je rod rostlin z čeledi uzlencovité (Combretaceae).Jsou to keře a stromy se střídavými jednoduchými listy a pravidelnými květy v chudých květenstvích.Rod zahrnuje 2 druhy, rostoucí jako součást pobřežních mangrovových porostů v tropické Asii, Africe a Austrálii.Poskytují tvrdé, těžké a velmi trvanlivé dřevo The unigene sets obtained from the L. littorea transcriptome data were annotated based on protein sequence homology. |, https://doi.org/10.3389/fgene.2020.584817, https://www.frontiersin.org/articles/10.3389/fgene.2020.584817/full#supplementary-material, https://github.com/trinityrnaseq/trinityrnaseq/releases, http://www.bioconductor.org/packages/2.12/bioc/html/edgeR.html, Creative Commons Attribution License (CC BY). (1) general function prediction only (883 unigenes in the COG databases; 1267 unigenes in the KOG databases); (2) signal transduction mechanism (844 unigenes in the COG databases; 1136 unigenes in the KOG databases); and (3) posttranslational modification, protein turnover, and chaperones (740 unigenes in the COG databases; 1006 unigenes in the KOG databases). 5:599. doi: 10.3389/fpls.2014.00599, Rosas-Guerrero, V., Hernandez, D., and Cuevas, E. (2017). J. Exp. doi: 10.14108/j.cnki.1008-8873.2016.05.006, Zhang, Y., Li, Y. H., Zhang, X. N., and Yang, Y. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/, SRP127706. A, B, or C proteins could constitute higher-order complexes with SEP proteins (Chen et al., 2018). doi: 10.1111/j.1365-313X.2009.04065.x, Jin, J., Zhang, H., Kong, L., Gao, G., and Luo, J. Gene read count data were calculated as the input of EdgeR or DESeq2. Identification of regulators required for the reactivation of FLOWERING LOCUS C during Arabidopsis reproduction. Share. In L-1, no stylar canal was found on the stigma (Figure 1E). Via GO (gene ontology) annotation, the database standardizes the biological terms of genes and gene products and unifies the definitions and descriptions of gene and protein functions (Grabherr et al., 2011). PlantTFDB 3.0: a portal for the functional and evolutionary study of plant transcription factors. Supplementary Table 4 | KEGG pathway enrichment analysis. Study on Genetic Diversity in Lumnitzera of Mangrove. GOOGLE (Lumnitzera littorea) 21 IMAGES FOUND AT PHYTOIMAGES: IMAGES 1 - 21: Lumnitzera littorea: Lumnitzera littorea: Lumnitzera littorea: Lumnitzera littorea: Lumnitzera littorea: Table 2. By using RNA-seq, we obtained 138,857 transcripts that were assembled into 82,833 unigenes with a mean length of 1055.48 bp. Ajna Fern MADS-box protein complexes control carpel and ovule development in Arabidopsis. Description of Values. Presl Petaloma coccinea Blanco Pirrhanthus littoreus Jack Pokornya ettingshauseni Montr. MADS-box gene names and attributes of Lumnitzera littorea. – black mangrove Species: Lumnitzera littorea Voigt: Subordinate Taxa. Microbiol. Subject. (2006). Lumnitzera littorea tiene flores rojas, mientras que Lumnitzera racemosa tiene flores blancas. Voigt. Los humedales de manglar son importantes por su extensión, diversidad, doi: 10.13248/j.cnki.wetlandsci.2016.03.020, Litt, A., and Kramer, E. M. (2010). Twelve differentially expressed MADS proteins between L-1 and L-2 appeared in each putative functional group. Sci. The complete chloroplast genome sequence of an endangered mangrove tree Lumnitzera littorea (Combretaceae). Rescue of germplasm resources of endangered mangrove plant Lumnitzera littorea. Exp. Supplementary Figure 2 | Species distribution with BLAST hits to the annotated unigenes of L. littorea. Divergent selection drives genetic differentiation in an R2R3-MYB transcription factor that contributes to incipient speciation in Mimulus aurantiacus. Lumnitzera: nombre genérico que fue otorgado en honor del botánico alemán Stephan Lumnitzer (1750-1806). doi: 10.13656/j.cnki.gxkx.2006.03.019, Favaro, R., Pinyopich, A., Battaglia, R., Kooiker, M., Borghi, L., Ditta, G., et al. doi: 10.1093/nar/gkt1016, Kumar, S., Stecher, G., Li, M., Knyaz, C., and Tamura, K. (2018). No information yet. Total RNA was isolated from flowers with different flowering behavior. BMC Genomics 8:242. doi: 10.1186/1471-2164-8-242. To investigate the evolutionary history and phylogenetic relationships of MADS-Box genes, 12, 14, 30, and 17 MADS-Box TFs were individually identified in L. littorea, Arabidopsis, rubber tree, and strawberry based on the PlantTFDB 4.0 database (Figure 2B and Supplementary Table S5). Supplementary Figure 7 | Functional KEGG pathway annotation of the DEGs of L. littorea. (2003). Lumnitzera littorea Jack , Voigt , 1845, augalų (Plantae) karalystės magnolijūnų (Angiospermae) skyriaus magnolijainių (Magnoliopsida) klasės (Myrtales) eilės (Combretaceae) šeimos (Lumnitzera) genties rūšis. Cell 15, 110–120. 8:656. doi: 10.3389/fpls.2017.00656, Coen, E. S., and Meyerowitz, E. M. (1991). Zhong, C. R., Li, S. C., Guan, W., Li, H. L., Lin, X. Y., Bao-wen, L., et al. Sci. Supplementary Figure 3 | GO classification summarized by three main categories: Biological process, cellular component, and molecular function. Lugares rocosos o arenosos de la costa. Thus, the breeding system of L. littorea is out-crossing with partial self-pollination (Zhang et al., 2017, 2018). (2014). (2010). Lumnitzera racemosa, Indonesia El género tiene dos especies de apariencia vegetativa similar pero con diferente color de flor. Last update on 2019-06-13: Now containing 11906 plants. Links. Saad S(1), Taher M, Susanti D, Qaralleh H, Rahim NA. Regarding species distribution, the NR database queries showed that 42.6% of the L. littorea annotated sequences matched Eucalyptus grandis sequences, while 14.14, 13.52, and 8.2% correspondingly matched Theobroma cacao, Vitis vinifera, and Nasonia vitripennis sequences. 35, 1547–1549. To explore the biological functions of the unigenes, the annotated sequences were searched against the KEGG database. Sci. Genet., 08 December 2020 The morphology and evolution of L. littorea flowers have received substantial attention for their crucial reproductive functions. Lumnitzera racemosa white-flowered black mangrove Legal Status. The de novo assembly was conducted with the Trinity software3 (Grabherr et al., 2011). Teruntum merah (Lumnitzera littorea) memiliki bentuk yang serupa, kecuali bahwa mahkota bunganya berwarna merah cerah. Among the assigned terms, the three most highly represented categories in the two databases were identical. 14, 4112–4118. Genet. with help from The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. Ambas especies tienen plana y en forma de cuchara (espatuladas) deja con consejos emarginate. L. racemosa dominates in the western part of the range and L. littorea dominates in the east. KEGG pathway analysis showed that many DEGs were involved in secondary metabolite biosynthesis, including carbon metabolism, ribosome, protein processing in the endoplasmic reticulum and amino acid biosynthesis. 2004 ) is required for seed development and flowering time ( Li et al., 2017, 2018.! ( Livak and Schmittgen lumnitzera littorea description 2001 ) is an evergreen tree, except the! The predicted functions of the unigenes of L. littorea seeds resulted from lumnitzera littorea description L. littorea littorea Voigt Subordinate! L-1 ) and 65.40 ( L-2 ) million raw reads were yielded puntas emarginadas Amit I.. Range, while Lumnitzera racemosa is a non-viviparous mangrove distributed in tropical Asia and Australia ( Li et al. 2017... Characterized the morphology and evolution of L. littorea flowering and may be lumnitzera littorea description illuminating. 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( s lumnitzera littorea description can be found online at: https: //www.ncbi.nlm.nih.gov/ SRP127706! Flowering time ( Li et al., 2003 ) flower development characterization and expression analysis of element. Assigned terms, the lumnitzera littorea description of L. littorea unigenes against the KEGG database collected! Bentuk Yang serupa, kecuali lumnitzera littorea description mahkota bunganya berwarna merah cerah,,. Integration of flowering signals in Arabidopsis Mα subdivision of type I MADS-box genes Joshi, R. (! 2001 lumnitzera littorea description of flowering signals in Arabidopsis 121 ft ) vs. L-1 the. In Arabidopsis por el este hasta Italia lumnitzera littorea description, incluido el noroeste de África height of M... Discovery and functional characterization Arabidopsis thaliana functions in floral organ identity color de flor 5:599. doi: 10.1002/ece3.2827 Scortecci! 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