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The proposed role of MSL-lncRNAs in causing sex lability of female poplars 被引量:1
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作者 jinyan mao Suyun Wei +2 位作者 Yingnan Chen Yonghua Yang Tongming Yin 《Horticulture Research》 SCIE CSCD 2023年第5期29-37,共9页
Labile sex expression is frequently observed in dioecious plants,but the underlying genetic mechanism remains largely unknown.Sex plasticity is also observed in many Populus species.Here we carried out a systematic st... Labile sex expression is frequently observed in dioecious plants,but the underlying genetic mechanism remains largely unknown.Sex plasticity is also observed in many Populus species.Here we carried out a systematic study on a maleness-promoting gene,MSL,detected in the Populus deltoides genome.Our results showed that both strands of MSL contained multiple cis-activating elements,which generated long non-coding RNAs(lncRNAs)promoting maleness.Although female P.deltoides did not have the male-specific MSL gene,a large number of partial sequences with high sequence similarity to this gene were detected in the female poplar genome.Based on sequence alignment,the MSL sequence could be divided into three partial sequences,and heterologous expression of these partial sequences in Arabidopsis confirmed that they could promote maleness.Since activation of the MSL sequences can only result in female sex lability,we propose that MSL-lncRNAs might play a role in causing sex lability of female poplars. 展开更多
关键词 FEMALE SIMILARITY alignment
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Tuning desolvation kinetics of in-situ weakly solvating polyacetal electrolytes for dendrite-free lithium metal batteries
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作者 Peng Wen Yimin Liu +8 位作者 jinyan mao Xiaotong Liu Weiping Li Yang Ren Yang Zhou Fei Shao mao Chen Jun Lin Xinrong Lin 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2023年第4期340-347,共8页
The host structure of polymers significantly influences ion transport and interfacial stability of electrolytes,dictating battery cycle life and safety for solid-state lithium metal batteries.Despite promising propert... The host structure of polymers significantly influences ion transport and interfacial stability of electrolytes,dictating battery cycle life and safety for solid-state lithium metal batteries.Despite promising properties of ethylene oxide-based electrolytes,their typical clamp-like coordination geometry leads to crowd solvation sheath and overly strong interactions between Li^(+)and electrolytes,rendering difficult dissociation of Li+and unfavorable solid electrolyte interface(SEI).Herein,we explore weakly solvating characteristics of polyacetal electrolytes owing to their alternately changing intervals between–O–coordinating sites in the main chain.Such structural asymmetry leads to unique distorted helical solvation sheath,and can effectively reduce Li^(+)-electrolyte binding and tune Li^(+)desolvation kinetics in the insitu formed polymer electrolytes,yielding anion-derived SEI and dendrite-free Li electrodeposition.Combining with photoinitiated cationic ring-opening polymerization,polyacetal electrolytes can be instantly formed within 5 min at the surface of electrode,with high segmental chain motion and well adapted interfaces.Such in-situ polyacetal electrolytes enabled more than 1300-h of stable lithium electrodeposition and prolonged cyclability over 200 cycles in solid-state batteries at ambient temperatures,demonstrating the vital role of molecular structure in changing solvating behavior and Li deposition stability for high-performance electrolytes. 展开更多
关键词 Polymer electrolyte In-situ photoinitiated polymerization Weakly solvating effect POLYACETAL Lithium electrodeposition
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