Shuilin He

Prof. Shuilin He

Key Laboratory of Applied Genetics of universities in Fujian Province, Fujian Agriculture and Forestry University
+1
orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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6 April 2015 in Journal of Experimental Botany
Verified
Journal Article
Closed access
HCHanyang Cai
Hanyang Cai
SYSheng Yang
Sheng Yang
YYYan Yan
Yan Yan
ZXZhuoli Xiao
Zhuoli Xiao
JCJunbin Cheng
Junbin Cheng
SHShuilin He
Shuilin He
High temperature (HT), high humidity (HH), and pathogen infection often co-occur and negatively affect plant growth. However, these stress factors and plant responses are generally studied in isolation. The mechanisms of synergistic responses to combined stresses are poorly understood. We isolated the subgroup IIb WRKY family member CaWRKY6 from Capsicum annuum and performed quantitative real-time PCR analysis. CaWRKY6 expression was upregulated by individual or simultaneous treatment with HT, HH, combined HT and HH (HTHH), and Ralstonia solanacearum inoculation, and responded to exogenous application of jasmonic acid (JA), ethephon, and abscisic acid (ABA). Virus-induced gene silencing of CaWRKY6 enhanced pepper plant susceptibility to R. solanacearum and HTHH, and downregulated the hypersensitive response (HR), JA-, ethylene (ET)-, and ABA-induced marker gene expression, and thermotolerance-associated expression of CaHSP24, ER-small CaSHP, and Chl-small CaHSP. CaWRKY6 overexpression in pepper attenuated the HTHH-induced suppression of resistance to R. solanacearum infection. CaWRKY6 bound to and activated the CaWRKY40 promoter in planta, which is a pepper WRKY that regulates heat-stress tolerance and R. solanacearum resistance. CaWRKY40 silencing significantly blocked HR-induced cell death and reduced transcriptional expression of CaWRKY40. These data suggest that CaWRKY6 is a positive regulator of R. solanacearum resistance and heat-stress tolerance, which occurs in part by activating CaWRKY40.

16 October 2013 in Physiologia Plantarum
Verified
Journal Article
Closed access
PDF file
FDFengfeng Dang
Fengfeng Dang
YWYuna Wang
Yuna Wang
JSJianju She
Jianju She
YLYufen Lei
Yufen Lei
ZLZhiqin Liu
Zhiqin Liu
SHShuilin He
Shuilin He

20 April 2017 in Frontiers in Plant Science
Verified
Journal Article
Open access
ANAli Noman
Ali Noman
MAMuhammad Aqeel
Muhammad Aqeel
JDJianming Deng
Jianming Deng
NKNoreen Khalid
Noreen Khalid
TSTayyaba Sanaullah
Tayyaba Sanaullah
SHShuilin He
Shuilin He
Developing new ornamental cultivars with improved floral attributes is a major goal in floriculture. Biotechnological approach together with classical breeding methods has been used to modify floral color, appearance as well as for increasing disease resistance. Transgenic strategies possess immense potential to produce novel flower phenotypes that are not found in nature. Adoption of Genetic engineering has supported the idea of floral trait modification. Ornamental plant attributes like floral color, fragrance, disease resistance and vase life can be improved by means of genetic manipulation. Therefore, we witness transgenic plant varieties of high aesthetic and commercial value. This review focuses on biotechnological advancements in manipulating key floral traits that contribute in development of diverse ornamental plant lines. Data clearly reveals that regulation of biosynthetic pathways related to characteristics like pigment production, flower morphology and fragrance is both possible and predictable. In spite of their great significance, small number of genetically engineered varieties of ornamental plants has been field tested. Today, novel flower colors production is regarded as chief commercial benefit obtained from transgenic plants. But certain other floral traits are much more important and have high commercial potential. Other than achievements such as novel architecture, modified flower color, etc. very few reports are available regarding successful transformation of other valuable horticultural characteristics. Our review also summarized biotechnological efforts related to enhancement of fragrance and induction of early flowering along with changes in floral anatomy and morphology.

1 March 2016 in Journal of Experimental Botany
Verified
Journal Article
Open access
PDF file
LSLei Shen
Lei Shen
ZLZhiqin Liu
Zhiqin Liu
SYSheng Yang
Sheng Yang
TYTong Yang
Tong Yang
JLJiaqi Liang
Jiaqi Liang
SHShuilin He
Shuilin He
CaWRKY40 is known to act as a positive regulator in the response of pepper (Capsicum annuum) to Ralstonia solanacearum inoculation (RSI) or high temperature–high humidity (HTHH), but the underlying mechanism remains elusive. Herein, we report that CabZIP63, a pepper bZIP family member, participates in this process by regulating the expression of CaWRKY40. CabZIP63 was found to localize in the nuclei, be up-regulated by RSI or HTHH, bind to promoters of both CabZIP63 (pCabZIP63) and CaWRKY40 (pCaWRKY40), and activate pCabZIP63- and pCaWRKY40-driven β-glucuronidase expression in a C- or G-box-dependent manner. Silencing of CabZIP63 by virus-induced gene silencing (VIGS) in pepper plants significantly attenuated their resistance to RSI and tolerance to HTHH, accompanied by down-regulation of immunity- or thermotolerance-associated CaPR1, CaNPR1, CaDEF1, and CaHSP24. Hypersensitive response-mediated cell death and expression of the tested immunity- and thermotolerance-associated marker genes were induced by transient overexpression (TOE) of CabZIP63, but decreased by that of CabZIP63-SRDX. Additionally, binding of CabZIP63 to pCaWRKY40 was up-regulated by RSI or HTHH, and the transcript level of CaWRKY40 and binding of CaWRKY40 to the promoters of CaPR1, CaNPR1, CaDEF1 and CaHSP24 were up-regulated by TOE of CabZIP63. On the other hand, CabZIP63 was also up-regulated transcriptionally by TOE of CaWRKY40. The data suggest collectively that CabZIP63 directly or indirectly regulates the expression of CaWRKY40 at both the transcriptional and post-transcriptional level, forming a positive feedback loop with CaWRKY40 during pepper's response to RSI or HTHH. Altogether, our data will help to elucidate the underlying mechanism of crosstalk between pepper's response to RSI and HTHH.

1 December 2021 in New Phytologist
Verified
Journal Article
Closed access
PDF file
SYSheng Yang
Sheng Yang
WCWeiwei Cai
Weiwei Cai
LSLei Shen
Lei Shen
JCJianshen Cao
Jianshen Cao
CLCailing Liu
Cailing Liu
SHShuilin He
Shuilin He

6 September 2017 in Biotechnology Letters
Verified
Journal Article
Closed access
PDF file
ANAli Noman
Ali Noman
ZLZhiqin Liu
Zhiqin Liu
MAMuhammad Aqeel
Muhammad Aqeel
MZMadiha Zainab
Madiha Zainab
MKMuhammad Ifnan Khan
Muhammad Ifnan Khan
SHShuilin He
Shuilin He