000 02290nam a22003017a 4500
003 ZW-GwMSU
005 20250220073509.0
008 250220b |||||||| |||| 00| 0 eng d
022 _a0176-1617
040 _aMSU
_bEnglish
_cMSU
_erda
050 0 0 _aQK711.2 JOU
100 1 _aHwang, Sun-Goo
_eauthor
245 1 0 _aMolecular characterization of Oryza sativa arsenic-induced RING E3 ligase 1 (OsAIR1): Expression patterns, localization, functional interaction, and heterogeneous overexpression
_ccreated by Sun-Goo Hwang, Hyeon Mi Park, A-Reum Han and Cheol Seong Jang
264 1 _aAmsterdam:
_bElsevier GmbH,
_c2016.
336 _2rdacontent
_atext
_btxt
337 _2rdamedia
_aunmediated
_bn
338 _2rdacarrier
_avolume
_bnc
440 _aJournal of plant physiology
_vVolume 191
520 3 _aHigh levels of arsenic (As) in plants are a serious threat to human health, and arsenic accumulation affects plant metabolism and ultimately photosynthesis, growth, and development. We attempted to isolate As-responsive Really Interesting New Gene (RING) E3 ubiquitin ligase genes from rice, and we have designated one such gene Oryza sativa arsenic-induced RING E3 ligase 1 (OsAIR1). OsAIR1 expression was induced under abiotic stress conditions, including drought, salt, heat, and As exposure. Results from an in vitro ubiquitination assay showed that OsAIR1 possesses E3 ligase activity. Within the cell, the expression of this gene was found to be localized to the vacuole. In a network-based analysis, we found significantly enriched gene ontology (GO) functions, which included ribonucleoprotein complexes such as ribosomes, suggesting that the function of OsAIR1 are related to translation. Differences in the proportion of seedlings with expanded cotyledons and root lengths, and the lack of differences in germination rates between OsAIR1-overexpressing lines and control plants under AsV stress, suggest that OsAIR1 may positively regulate post-germination plant growth under stress conditions.
650 _aArsenic
650 _aAbiotic stress
650 _aRice
700 1 _aMi Park, Hyeon
_eco-author
700 1 _aHan, A-Reum
_eco-author
700 1 _aJang, Cheol Seong
_eco-author
856 _uhttps://doi.org/10.1016/j.jplph.2015.12.010
942 _2lcc
_cJA
999 _c169005
_d169005