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Details for: GSOR 100,
Oryza sativa
L., NIPPONBARE
Summary
Passport
Taxonomy
Other
Pedigree
IPR
Observation
Summary Data
Taxonomy:
Oryza sativa
L.
Top Name:
NIPPONBARE
Origin:
Developed – Arkansas, United States
Maintained:
Rice Genetic Stock Center
Received by NPGS:
01 Jan 2004
Improvement Status:
Genetic material
Form Received:
Seed
Life Form:
Annual
Life Cycle:
Annual
Availability
Form
Quantity
Note
Inventory
Cart
Seed
100 gram
GSOR 100 A21FA3 SD
There are no images for this accession.
Core Passport Data
Taxonomy:
Oryza sativa
L.
Top Name:
NIPPONBARE
Origin:
Developed – Arkansas, United States
Maintained:
Rice Genetic Stock Center
Received by NPGS:
01 Jan 2004
Improvement Status:
Genetic material
Form Received:
Seed
Life Form:
Annual
Life Cycle:
Annual
Source History
Developed
2004.
Arkansas, United States
Developer(s):
Rutger, J. Neil
Accession Names and Identifiers
NIPPONBARE
Type: Developer identifier
Group: NIPPONBARE
GSOR 100
Type: Site identifier
Group: NIPPONBARE
Narrative
This material, descended via Cornell, is from the single plant selection identified by Dr. T. Sasaki of Japan, for the International Rice Gene Sequencing Project.
Oryza sativa
L.
Genus:
Oryza
Section:
Oryza
Subsection:
Oryza
Family:
Poaceae
(alt. Gramineae)
Subfamily:
Oryzoideae
Tribe:
Oryzeae
Subtribe:
Oryzinae
Nomen number:
26077
Place of publication:
Sp. pl. 1:333. 1753
Protologue link:
https://biodiversitylibrary.org/page/358352
Comment:
some seed lots of domesticated rice may contain contaminants of a noxious weed hybrid-form that are not distinguishable by seed visualization, which is responsible for the rice-growing state's noxious-weed seed regulations indicated below
Typification:
View in Linnean Typification Project
Verified:
05/11/1992
by ARS Systematic Botanists.
Other conspecific taxa
Autonyms (not in current use), synonyms and invalid designations
Autonym(s)
Oryza sativa
L. f.
sativa
Oryza sativa
L. subsp.
sativa
Oryza sativa
L. var.
sativa
Heterotypic Synonym(s)
Oryza glutinosa
Lour.
Oryza sativa
L. var.
erythroceros
Körn.
Oryza sativa
L. var.
italica
Alef.
Oryza sativa
L. var.
vulgaris
Körn.
Oryza sativa
L. var.
zeravschanica
Brches ex Katzaroff, nom. nud.
Oryza sativa
L. subsp.
indica
Kato
Oryza sativa
L. var.
affinis
Körn.
Oryza sativa
L. var.
melanacra
Körn.
Oryza sativa
L. var.
flavoacies
Kara-Murza ex Zhuk.
Oryza sativa
L. var.
suberythroceros
Kanevsk
Oryza sativa
L. subsp.
japonica
Kato
Oryza sativa
L. var.
japonica
auct.
Oryza communissima
Lour.
Oryza formosana
Masam. & Suzuki
Oryza montana
Lour.
Common names
Language
Name
Alternate name
note
seq
Citation
English
Asian rice
1
Hanelt, P., ed.
2001.
Mansfeld's encyclopedia of agricultural and horticultural crops. Volumes 1-6
English
lowland rice
1
Hanelt, P., ed.
2001.
Mansfeld's encyclopedia of agricultural and horticultural crops. Volumes 1-6
English
rice
1
Wiersema, J. H. & B. León.
1999.
World economic plants: a standard reference
CRC Press, Boca Raton, FL.
English
upland rice
1
Hanelt, P., ed.
2001.
Mansfeld's encyclopedia of agricultural and horticultural crops. Volumes 1-6
Arabic
rozz
2
Boulos, L.
1999-. Flora of Egypt
French
riz
2
Rehm, S.
1994. Multilingual dictionary of agronomic plants
German
Reis
2
Rehm, S.
1994. Multilingual dictionary of agronomic plants
India
chavel
2
Rehm, S.
1994. Multilingual dictionary of agronomic plants
Italian
riso
2
Hanelt, P., ed.
2001.
Mansfeld's encyclopedia of agricultural and horticultural crops. Volumes 1-6
Japanese Rōmaji
ine
2
Batra, L. R.
1995. Names of Japanese plants sorted by their Japanese names in Romanized Katakana and scientific nomenclature
Portuguese
arroz
2
Rehm, S.
1994. Multilingual dictionary of agronomic plants
Spanish
arroz
2
Rehm, S.
1994. Multilingual dictionary of agronomic plants
Swedish
ris
2
Aldén, B., S. Ryman, & M. Hjertson.
2012.
Svensk Kulturväxtdatabas, SKUD (Swedish Cultivated and Utility Plants Database; online resource)
Transcribed Chinese
dao
2
Wu Zheng-yi & P. H. Raven et al., eds.
1994-.
Flora of China (English edition).
Name
References
Annotations
Other Links
Actions
Pathogens
Vouchers
Citations
Atighi, M. R., B. Verstraeten, T. De Meyer, & T. Kyndt.
2020. Genome-wide DNA hypomethylation shapes nematode pattern-triggered immunity in plants. New Phytol. 227:545-558.
Number of accessions cited:
1
Chen, M.-S., X. Liu, H. Wang, & M. El-Bouhssini.
2009. Hessian Fly (Diptera: Cecidomyiidae) interactions with barley, rice, and wheat seedlings. J. Econ. Entomol. 102(4)1663-1672.
Number of accessions cited:
1
Deshpande, A., S. R. Dhadi, E. J. Hager, & W. Ramakrishna.
2011. Anticancer activity of rice callus suspension culture. Phytotherapy Res. 26:1075-1081.
DOI:
10.1002/ptr.3699
.
Number of accessions cited:
1
Dhadi, S. R., A. Deshpande, & W. Ramakrishna.
2012. A novel non-wounding transient expression assay for cereals mediated by
Agrobacterium tumefaciens
. Pl. Molec. Biol. Reporter 30:36-45.
DOI:
10.1007/s11105-011-0314-5
.
Note:
ISSN: 0735-9640 (Print) 1572-9818 (Online)
Number of accessions cited:
1
Hongli, Ji, G. Gheysen, C. Ullah, R. Verbeek, C. Shang, D. De Vleesschauwer, M. Hofte, & T. Kyndt.
2015. The role of thionins in rice defence against root pathogens. Molec. Pl. Pathol. 16(8):870-881.
DOI:
10.1111/mpp.12246
.
Number of accessions cited:
1
Huang, Wen-kun, Hong-Li Ji, G. Gheysen, & T. Kyndt.
2016. Thiamine-induced priming against root-knot nematode infection in rice involves lignification and hydrogen peroxide generation. Molec. Pl. Pathol. 17(4):614-624.
DOI:
10.1111/mpp.12316
.
Number of accessions cited:
1
Huang, Wen-kun, Hong-Li Ji, G. Gheysen, J. Debode, & T. Kyndt.
2015. Biochar-amended potting medium reduces the susceptibility of rice to root-knot nematode infections. B. M. C. Pl. Biol. 15:267.
DOI:
10.1186/s12870-015-0654-7
.
Number of accessions cited:
1
Janevska, S., U. Guldener, M. Sulyok, B. Tudzynski, & L. Studt.
2018. Set1 and Kdm5 are antagonists for H3K4 methylation and regulators of the major conidiation-specific transcription factor gene
ABA1
in
Fusarium fujikuroi
. Environm. Microbiol. 20(9):3343-3362.
DOI:
10.1111/1462-2920.14339
.
Number of accessions cited:
1
Ji, H. et al.
2015. β-aminobutyric acid-induced resistance against root-knot nematodes in rice is based on increased basal defence. Molec. Pl.-Microbe Interact.
Note:
PMID: 25608179
Number of accessions cited:
1
Karan, R., T. De Leon, H. Biradar, & P.K. Subudhi.
2012. Salt stress induced variation in DNA methylation pattern and its influence on gene expression in contrasting rice genotypes. PLoS One 7(6)e40203.
Number of accessions cited:
1
Koelmel, J., T. Leland, H. Wang, D. Amarasiriwardena, & B. Xing.
2013. Investigation of gold nanoparticles uptake and their tissue level distribution in rice plants by laser ablation-inductively coupled-mass spectrometry. Environm. Pollut. 174:222-228.
DOI:
10.1016/j.envpol.2012.11.026
.
Number of accessions cited:
1
Kyndt, T. et al.
2012. Transcriptome analysis of rice mature root tissue and root tips in early development by massive parallel sequencing. J. Exp. Bot. 63:2141-2157.
DOI:
10.1093/jxb/err435
.
Number of accessions cited:
1
Kyndt, T., H. Y. Zemene, A. Haeck, R. Singh, D.De Vleesschauwer, S. Denil, T. De Meyer, M. Hofte, K. Demeestere, & G. Gheysen.
2017. Below-ground attack by the root knot nematode
Meloidogyne graminicola
predisposes rice to blast disease. Molec. Pl.-Microbe Interact.
DOI:
10.1094/MPMI-11-16-0225-R
.
Number of accessions cited:
1
Kyndt, T., K. Nahar, A. Haeck, R. Verbeek, K. Demeestere, & G. Gheysen.
2017. Interplay between carotenoids, abscisic acid and jasmonate guides the compatible rice-
Meloidogyne gramnicola
interaction. Front. Plant Sci. 8:951.
DOI:
10.3389/fpls.2017.00951
.
Number of accessions cited:
1
Kyndt, T., K. Nahar, A. Haegeman, D. De Vleesschauwer, M. Hofte, & G. Gheysen.
2011. Comparing systemic defence-related gene expression changes upon migratory and sedentary nematode attack in rice. Pl. Biol. 14(s1):73-82.
DOI:
10.1111/j.1438-8677.2011.00524.x
.
Number of accessions cited:
1
Kyndt, T., S. Denil, A. Haegeman, G. Trooskens, L. Bauters, W. V. Criekinge, T. De Meyer, & G. Gheysen.
2012. Transcriptional reprogramming by root knot and migratory nematode infection in rice. New Phytol. 196:887-900.
DOI:
10.1111/j.1469-8137.2012.04311.x
.
Number of accessions cited:
1
Kyndt, T., S. Denil, L. Bauters, W. V. Criekinge, & T. De Meyer.
2014. Systemic suppression of the shoot metabolism upon rice root nematode infection. PLoS One 9(9):e106858.
Number of accessions cited:
1
Lakshmanan, L., J. Cottone, & H.P. Bais.
2016. Killing two birds with one stone: natural rice rhizospheric microbes reduce arsenic uptake and blast infections in rice. Front. Plant Sci. 7:1514.
DOI:
10.3389/fpls.2016.01514
.
Number of accessions cited:
1
Lubkowitz, M.
2011. The oligopeptide transporters: a small gene family with a diverse group of substrates and functions? Molec. Pl. pp. 1-9.
DOI:
10.1093/mp/ssr004
.
Note:
4(3):407-415.
Number of accessions cited:
1
Nahar, K., T. Kyndt, D. De Vleesschauwer, M. Hofte, & G. Gheysen.
2011. The jasmonate pathway is a key player in systemically induced defense against root knot nematodes in rice. Pl. Physiol. (Lancaster) 157:305-316.
DOI:
10.1104/pp.111.177576
.
Number of accessions cited:
1
Nahar, K., T. Kyndt, Y. B. Nzogela, & G. Gheysen.
2012. Abscisic acid interacts antagnostically with classical defense pathways in rice-migratory nematode interaction. New Phytol. 196:901-913.
DOI:
10.1111/j.1469-8137.2012.04310.x
.
Number of accessions cited:
1
Pokhrel, S., S. K. Ponniah, Y. Jia, O. Yu, & M. Manoharan.
2021. Transgenic rice expressing isoflavone synthase gene from soybean shows resistance against blast fungus (
Magnaporthe oryzae
). Pl. Dis.
DOI:
10.1094/PDIS-08-20-1777-RE
.
Number of accessions cited:
1
Ponniah, S. K., Z. Shang, M. A. Akbudak, V. Srivastava, & M. Manoharan.
2017. Down-regulation of hydroxycinnamoyl CoA: shikimate hydroxycinnamoyl transferase, cinnamoyl CoA reductase, and cinnamoyl alcohol dehydrogenase leads to lignin reduction in rice (
Oryza sativa
L. ssp.
japonica
cv. Nipponbare). Pl. Biotechnol. J. 11:17-27.
DOI:
10.1007/s11816-017-0426-y
.
Number of accessions cited:
1
Singh, R. R. et al.
2019. Systemic defense activation by COS-OGA in rice against root-knot nematodes depends on stimulation of the phenylpropanoid pathway. Plant Physiol. Biochem. 142:202-210.
DOI:
10.1016/j.plaphy.2019.07.003
.
Number of accessions cited:
1
Singh, R. R. et al.
2020. Ascorbate oxidation activates systemic defence against root-knot nematode
Meloidogyne graminicola
in rice. J. Exp. Bot. 71:4271-4284.
DOI:
10.1093/jxb/eraa171
.
Number of accessions cited:
1
Thilmony, R., M. Guttman, J. G. Thomson, & A. E. Blechl.
2009. The
LP2
leucine-rich repeat receptor kinase gene promoter directs organ-specific, light-responsive expression in transgenic rice. Pl. Biotechnol. J. 7:867-882.
DOI:
10.000/j.1467-7652.2009.00449.x
.
Number of accessions cited:
1
Thomas, J. et al.
2019. RNA-seq reveals differentially expressed genes in rice (
Oryza sativa
) roots during interactions with plant-growth promoting bacteria,
Azospirillum brasilense
. PLoS One 14(5):e0217309.
DOI:
10.1371/journal.pone.0217309
.
Number of accessions cited:
1
Thomas, J., R. Histenbrand, M. J. Bowman, H. R. Kim, M. E. Winn, & A. Mukherjee.
2020. Time-course RNA-seq analysis provides an improved understanding of gene regulation during the formation of nodule-like structures in rice. Pl. Molec. Biol.
DOI:
10.1007/s11103-020-00978-0
.
Number of accessions cited:
1
Wu, Yufeng, Wenli Zhang, & Jiming Jiang.
2014. Genome-wide nucleosome positioning is orchestrated by genomic regions associated with DNase I hypersensitivity in rice. PLoS Genet. 10(5).
Note:
e1004378
Number of accessions cited:
1
Yan, H., P. B. Talbert, H. R. Lee, J. Jett, S. Henikoff, et al.
2008. Intergenic locations of rice centromeric chromatin. PLoS Biol. 6(11):e286.
DOI:
10.1371/journal.pbio.0060286
.
Number of accessions cited:
1
Yan, Huihuang, S. Kikuchi, P. Neumann, W. Zhang, Y. Wu, F. Chen, & J. Jiang.
2010. Genome-wide mapping of cytosine methylation revealed dynamic DNA methylation patterns associated with genes and centromeres in rice. Plant J. 63:353-365.
Number of accessions cited:
1
Zhang, Tao, et al.
2013. The
CentO
satellite confers translational and rotational phasing on cenH3 nucleosomes in rice centromeres. Proc. Natl. Acad. Sci. U.S.A. 110(50)e4875-e4883.
DOI:
10.1073/pnas.1319548110
.
Number of accessions cited:
1
Zhang, Wenli, et al.
2012. High-resolution mapping of open chromatin in the rice genome. Genome Res. 22:151-162.
DOI:
10.1101/gr.131342.111
.
Number of accessions cited:
1
Zhu, Zheng-Jiang, et al.
2012. Effect of surface charge on the uptake and distribution of gold nanoparticles in four plant species. Environm. Sci. Technol. 46:12391-12398.
Number of accessions cited:
1
Pedigree
Material Transfer Agreement
Observations
Phenotype Data
Category
Descriptor
Description
Value
Sample Size
Study
Inventory
Availability
PHENOLOGY
Days to Flower
Days from emergence to flowering. Actual values. See also related descriptor Days to Anthesis.
83
GSOR.2017.FIELD.OBS
GSOR 100 A18FA3 SD
Not Available