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  • 1
    Publication Date: 2014-03-18
    Description: Background: Lilium lancifolium, a very important cold-resistant wild flower for lily cold resistance breeding, is widely distributed in southwestern and northeastern China. To gain a better understanding of the cold signaling pathway and the molecular metabolic reactions involved in the cold response, we performed a genome-wide transcriptional analysis using RNA-Seq. Results: Approximately 104,703 million clean 90- bp paired-end reads were obtained from three libraries (CK 0 h, Cold-treated 2 h and 16 h at 4[degree sign]C); 18,736 unigenes showed similarity to known proteins in the Swiss-Prot protein database, and 15,898, 13,705 and 1849 unigenes aligned to existing sequences in the KEGG and COG databases (comprising 25 COG categories) and formed 12 SOM clusters, respectively. Based on qRT-PCR results, we studied three signal regulation pathways --the Ca2+ and ABA independent/dependent pathways --that conduct cold signals to signal transduction genes such as LlICE and LlCDPK and transcription factor genes such as LlDREB1/CBF, LlAP2/EREBP, LlNAC1, LlR2R3-MYB and LlBZIP, which were expressed highly in bulb. LlFAD3, Llbeta-amylase, LlP5CS and LlCLS responded to cold and enhanced adaptation processes that involve changes in the expression of transcripts related to cellular osmoprotectants and carbohydrate metabolism during cold stress. Conclusions: Our study of differentially expressed genes involved in cold-related metabolic pathways and transcription factors facilitated the discovery of cold-resistance genes and the cold signal transcriptional networks, and identified potential key components in the regulation of the cold response in L lancifolium, which will be most beneficial for further research and in-depth exploration of cold-resistance breeding candidate genes in lily.
    Electronic ISSN: 1471-2164
    Topics: Biology
    Published by BioMed Central
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  • 2
    Publication Date: 2013-04-01
    Description: In this paper, an integrated indicator-based system is established to map the suitability of spring soybean cultivation in northeast China. The indicator system incorporates both biophysical and socioeconomic factors, including the effects of temperature, precipitation, and sunshine on the individual development stages of the spring soybean life cycle. Spatial estimates of crop suitability derived using this indicator system are also compared with spring soybean planting areas to identify locations where there is scope for structural adjustment in soybean farming. Results of this study indicate that northeast China is moderately suited to spring soybean cultivation. Areas classified as suitable, moderately suitable, and unsuitable for soybean cultivation, respectively, occupy approximately 9.09 × 104, 11.45 × 104, and 7.99 × 104 km2, accounting for 11.5%, 10.11%, and 14.49% of the total area of northeast China. The Songnen and Sanjiang Plains are identified as the most and least suitable places, respectively, for spring soybean growth. A comparative analysis indicates that the suitable, moderately suitable, and unsuitable areas account for 24.78%, 46.30%, and 28.92%, respectively, of the total area presently under soybean cultivation. The analysis suggests that soybean cultivation in Heilongjiang Province is generally unfavorable, with equivalent percentages of 15.39%, 51.70%, and 32.91%. Results suggest that agricultural structural adjustment may be required to encourage farmers to grow spring soybeans. It is anticipated that this study will provide a basis for follow-up studies on crop cultivation suitability.
    Print ISSN: 1558-8424
    Electronic ISSN: 1558-8432
    Topics: Geography , Physics
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  • 3
    Publication Date: 2011-05-05
    Description: Background LINE-1s (L1, Long Interspersed Element-1) are the most abundant autonomous non-LTR retrotransposons in the human genome and replicate by reverse transcription of an RNA intermediate. Full-length L1 encodes two open reading frames (ORF1, ORF2) and ORF2 has reverse transcriptase activity. Results Here we expressed human L1 RT in E. coli and the purified protein displayed the same RT activity as that of ORF2p expressed in insect cells. We tested the effect of different reverse transcriptase inhibitors on L1 RT and found that all four tested nucleoside inhibitors efficiently inhibited L1 RT activity competitively. The Ki values of NRTIs were calculated (AZTTP, 16.4 ± 4.21 nM; d4TTP, 0.73 ± 0.22 nM; ddCTP, 0.72 ± 0.16 nM; 3TCTP, 12.9 ± 2.07 nM). L1 RT was less sensitive to non-nucleoside reverse transcriptase inhibitors, among these nevirapine had no effect, even at concentrations up to 500 μM. We also examined the effect of RT inhibitors on L1 retrotransposition efficiency in vivo using a cell-based retrotransposition assay. Similarly, all analog inhibitors decreased L1 retrotransposition frequency with different potencies whereas nevirapine had little or no effect on L1 retrotransposition. For comparison, we also tested the same inhibitors to highly purified RT of an LTR-retrotransposon (Ty1) and found it was less sensitive to NRTIs than L1 RT and has the same inhibition profile as L1 RT to NNRTIs. Conclusions These data indicate that bacterially expressed L1 RT is an active reverse transcriptase sensitive to nucleoside RT inhibitors but not to non-nucleoside inhibitors.
    Electronic ISSN: 1471-2091
    Topics: Chemistry and Pharmacology
    Published by BioMed Central
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