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| 1 | A genome-wide analysis of SWEET gene family in cotton and their expressions under different stresses显示文摘Background: The SWEET(Sugars will eventually be exported transporters) gene family plays multiple roles in plant physiological activities and development process. It participates in reproductive development and in the process of sugar transport and absorption, plant senescence and stress responses and plant-pathogen interaction. However,thecomprehensive analysis of SWEET genes has not been reported in cotton.Results: In this study, we identified 22, 31, 55 and 60 SWEET genes from the sequenced genomes of Gossypium arboreum, G. raimondii, G. hirsutum and G. barbadense, respectively. Phylogenetic tree analysis showed that the SWEET genes could be divided into four groups, which were further classified into 14 sub-clades. Further analysis of chromosomal location, synteny analysis and gene duplication suggested that the orthologs showed a good collinearity and segmental duplication events played a crucial role in the expansion of the family in cotton. Specific MtN3_slv domains were highly conserved between Arobidopsis and cotton by exon-intron organization and motif analysis. In addition, the expression pattern in different tissues indicated that the duplicated genes in cotton might have acquired new functions as a result of sub-functionalization or neo-funtionalization. The expression pattern of SWEET genes showed that the different genes were induced by diverse stresses. The identification and functional analysis of SWEET genes in cotton may provide more candidate genes for genetic modification.Conclusion: SWEET genes were classified into four clades in cotton. The expression patterns suggested that the duplicated genes might have experienced a functional divergence. This work provides insights into the evolution of SWEET genes and more candidates for specific genetic modification, which will be useful in future research. | ZHAO Lanjie YAO Jinbo CHEN Wei LI Yan L Youjun GUO Yan WANG Junyi YUAN Li LIU Ziyang ZHANG Yongshan | 2018 | Journal of Cotton Research2018，1，2： | 6 |
| 2 | Ultra-deep desulfurization of diesel by selective oxidation with4catalyst assembled in emulsion droplets显示文摘 | LüHongying Gao Jinbo Jiang Zongxuan | 2006 | Journal of Catalysis2006，239，2： | 1 |
| 3 | Ultra-deep desulfurization of diesel by selective oxidation with [C 18 H 37 N(CH 3 ) 3 ] 4 [H 2 NaPW 10 O 36 ] catalyst assembled in emulsion droplets显示文摘 | Hongying Lü Jinbo Gao Zongxuan Jiang Fei Jing Yongxing Yang Gang Wang Can Li | 2006 | Journal of Catalysis2006，，2： | 1 |
| 4 | Circulating plateletactivating factor isprimarily cleared by transport, not intravascular hydrolysis bylipoprotein-associated phospholipase A2/ PAF acetylhydrolase 显示文摘 | Jinbo L Rui C Gopal K | 2011 | Circ Res2011，108，4： | 1 |
| 5 | Ameliorative Effect of Ginsenoside RT-5 on CDDP-Induced Nephrotoxicity显示文摘The aim of this study is to explore whether RT-5, one novel active ginsenosides from Ginseng, has protective effects against cisplatin(CDDP)-induced nephrotoxicity in vivo. One model of acute renal failure induced by CDDP in rats and one model of xenograft tumors of human cervical cancer in nude mice are established. Four groups are assigned: control, CDDP, RT-5, CDDP plus RT-5, in which the RT-5 is administered via oral gavage 24 h before CDDP intraperitoneal injection. The significant increase in blood urea nitrogen and creatinine are induced by CDDP treatment at 6 mg/kg, which are attenuated by pre-treated with RT-5 at 10 mg/kg. RT-5 could ameliorate CDDP-induced morphological damages in kidney by PAS staining, and reduce tubular apoptosis evaluated by TUNEL staining. Pretreatment with RT-5 notably inhibits CDDP-induced oxidative stress in kidney tissues. Interestingly, RT-5 does not interfere with the in vivo anti-cancer effects of CDDP against the growth of xenograft tumors in nude mice. These data suggest that co-treatment RT-5 with CDDP might attenuate the following nephrotoxicity without inhibiting its anti-tumor efficiency, which could provide one novel strategy for cancer treatment in clinics. | JIANG Yongtao QIU Xiaolei MA Jinbo Lü Guangyao WANG Zongliang ZHANG Jingwen FU Fenghua WANG Hongbo | 2015 | Wuhan University Journal of Natural Sciences2015，20，4： | 1 |
| 6 | Ultra-deep desulfurization of diesel by selective oxidation with [C 18 H 37 N(CH 3 ) 3 ] 4 [H 2 NaPW 10 O 36 ] catalyst assembled in emulsion droplets显示文摘 | Hongying Lü Jinbo Gao Zongxuan Jiang Fei Jing Yongxing Yang Gang Wang Can Li | 2006 | Journal of Catalysis2006，，2： | 1 |
| 7 | Circulating platelet- activating factor is primarily cleared by transport, not intravascular hydrolysis by hpeprotein-associated phospholipase A2/PAF acetylhydrolase 显示文摘 | JINBO L RUI C G OPAL K | 2011 | Circ Res2011，108，4： | 1 |
| 8 | The exploration of macrocycles for drug discovery : an underexploited structural class 显示文摘 | Edward M D Stephen P H Jinbo L | 2008 | Nature2008，7，： | 1 |
| 9 | Geographic distance and pH drive bacterial distribution in alkaline lake sediments across Tibetan Plateau 显示文摘 | Jinbo X Yongqin L Xiangui L | 2012 | Environmental Microbiology2012，14，9： | 1 |
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