2015
DOI: 10.3390/ijms161126006
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CpLEA5, the Late Embryogenesis Abundant Protein Gene from Chimonanthus praecox, Possesses Low Temperature and Osmotic Resistances in Prokaryote and Eukaryotes

Abstract: Plants synthesize and accumulate a series of stress-resistance proteins to protect normal physiological activities under adverse conditions. Chimonanthus praecox which blooms in freezing weather accumulates late embryogenesis abundant proteins (LEAs) in flowers, but C. praecox LEAs are little reported. Here, we report a group of five LEA genes of C. praecox (CpLEA5, KT727031). Prokaryotic-expressed CpLEA5 was employed in Escherichia coli to investigate bioactivities and membrane permeability at low-temperature… Show more

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Cited by 37 publications
(13 citation statements)
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“…Ca 2+ has been identi ed to play a mediating role during plant SE [37,101]. LEA5, a late embryogenesis abundant proteins gene, was highly expressed in late embryogenesis [102]. In our study, SERK1, CML13, CML36 and CAM-7 were up-regulated in CE.…”
Section: Discussionsupporting
confidence: 53%
“…Ca 2+ has been identi ed to play a mediating role during plant SE [37,101]. LEA5, a late embryogenesis abundant proteins gene, was highly expressed in late embryogenesis [102]. In our study, SERK1, CML13, CML36 and CAM-7 were up-regulated in CE.…”
Section: Discussionsupporting
confidence: 53%
“…LEA5 belonged to the fifth group of late embryogenesis abundant proteins gene, were abundant in late embryogenesis of mature seed, and involved in the abiotic stresses responses [119]. CNOT3 , might be a new CCR4-NOT complex gene in plant, which had proved in regulation of cell division in HeLa cell, while its functions on plant was poorly-understood.…”
Section: Discussionmentioning
confidence: 99%
“…Studies on Ch. praecox have focused on transcriptomic and proteomic profiling throughout flower development [13,14,15,16]; fragrance gene identification [17]; floral scent emission from nectaries on the adaxial side of the innermost and middle petals [18]; separation and determination of volatile compounds [19,20], phenolic compounds [21], alkaloids and flavonoids [22,23,24], and sesquiterpenoids [25]; in vitro culture system development [26]; genetic linkage map construction [27]; simple sequence repeat (SSR) [28], expressed sequence tag (EST) [29], and amplified fragment length polymorphism (AFLP) [30] development; and ANL2 [31], CpAGL2 [32], CpAP3 [33], CpCAF1 [34], CpCZF1/2 [35], Cpcor413pm1 [36], CpEXP1 [37], CpH3 [38], CpLEA5 [39], Cplectin [29], CpNAC8 [40], CpRALF [41], CpRBL [42], FPPS [43], and G6PDH1 [44] cloning and development. Studies on Ch.…”
Section: Introductionmentioning
confidence: 99%