Jiangqi Wen

Dr. Jiangqi Wen

orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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1 July 2002 in Cell
Verified
Journal Article
Closed access
JLJia Li
Jia Li
Jiangqi WenJiangqi Wen
Jiangqi Wen
KLKevin A Lease
Kevin A Lease
JDJason T Doke
Jason T Doke
FTFrans E. Tax
Frans E. Tax
JWJohn C Walker
John C Walker

16 January 2008 in The Plant Journal
Verified
Journal Article
Closed access
PDF file
MTMillion Tadege
Million Tadege
Jiangqi WenJiangqi Wen
Jiangqi Wen
JHJi He
Ji He
HTHaidi Tu
Haidi Tu
YKYounsig Kwak
Younsig Kwak
KMKirankumar Mysore
Kirankumar Mysore

19 December 2014 in The Plant Cell
Verified
Journal Article
Open access
PDF file
ABAndrew Breakspear
Andrew Breakspear
CLChengwu Liu
Chengwu Liu
SRSonali Roy
Sonali Roy
NSNicola Stacey
Nicola Stacey
CRChristian Rogers
Christian Rogers
Jeremy MurrayJeremy Murray
Jeremy Murray
Nitrogen-fixing rhizobia colonize legume roots via plant-made intracellular infection threads. Genetics has identified some genes involved but has not provided sufficient detail to understand requirements for infection thread development. Therefore, we transcriptionally profiled Medicago truncatula root hairs prior to and during the initial stages of infection. This revealed changes in the responses to plant hormones, most notably auxin, strigolactone, gibberellic acid, and brassinosteroids. Several auxin responsive genes, including the ortholog of Arabidopsis thaliana Auxin Response Factor 16, were induced at infection sites and in nodule primordia, and mutation of ARF16a reduced rhizobial infection. Associated with the induction of auxin signaling genes, there was increased expression of cell cycle genes including an A-type cyclin and a subunit of the anaphase promoting complex. There was also induction of several chalcone O-methyltransferases involved in the synthesis of an inducer of Sinorhizobium meliloti nod genes, as well as a gene associated with Nod factor degradation, suggesting both positive and negative feedback loops that control Nod factor levels during rhizobial infection. We conclude that the onset of infection is associated with reactivation of the cell cycle as well as increased expression of genes required for hormone and flavonoid biosynthesis and that the regulation of auxin signaling is necessary for initiation of rhizobial infection threads.

1 November 2019 in Current Biology
Verified
Journal Article
Open access
KSKatharina Schiessl
Katharina Schiessl
JLJodi L.S. Lilley
Jodi L.S. Lilley
TLTak Lee
Tak Lee
ITIoannis Tamvakis
Ioannis Tamvakis
WKWouter Kohlen
Wouter Kohlen
GOGiles E.D. Oldroyd
Giles E.D. Oldroyd
To overcome nitrogen deficiencies in the soil, legumes enter symbioses with rhizobial bacteria that convert atmospheric nitrogen into ammonium. Rhizobia are accommodated as endosymbionts within lateral root organs called nodules that initiate from the inner layers of Medicago truncatula roots in response to rhizobial perception. In contrast, lateral roots emerge from predefined founder cells as an adaptive response to environmental stimuli, including water and nutrient availability. CYTOKININ RESPONSE 1 (CRE1)-mediated signaling in the pericycle and in the cortex is necessary and sufficient for nodulation, whereas cytokinin is antagonistic to lateral root development, with cre1 showing increased lateral root emergence and decreased nodulation. To better understand the relatedness between nodule and lateral root development, we undertook a comparative analysis of these two root developmental programs. Here, we demonstrate that despite differential induction, lateral roots and nodules share overlapping developmental programs, with mutants in LOB-DOMAIN PROTEIN 16 (LBD16) showing equivalent defects in nodule and lateral root initiation. The cytokinin-inducible transcription factor NODULE INCEPTION (NIN) allows induction of this program during nodulation through activation of LBD16 that promotes auxin biosynthesis via transcriptional induction of STYLISH (STY) and YUCCAs (YUC). We conclude that cytokinin facilitates local auxin accumulation through NIN promotion of LBD16, which activates a nodule developmental program overlapping with that induced during lateral root initiation.

4 January 2016 in New Phytologist
Verified
Journal Article
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PLPenghui Li
Penghui Li
BCBeibei Chen
Beibei Chen
GZGaoyang Zhang
Gaoyang Zhang
LCLongxiang Chen
Longxiang Chen
QDQiang Dong
Qiang Dong
JZJian Zhao
Jian Zhao

28 October 2010 in The Plant Journal
Verified
Journal Article
Open access
PDF file
Jeremy MurrayJeremy Murray
Jeremy Murray
RMRajaSekhara Reddy Duvvuru Muni
RajaSekhara Reddy Duvvuru Muni
ITIvone Torres‐Jerez
Ivone Torres‐Jerez
YTYuhong Tang
Yuhong Tang
SAStacy Allen
Stacy Allen
MUMichael K Udvardi
Michael K Udvardi
Summary: Intracellular invasion of root cells is required for the establishment of successful endosymbioses in legumes of both arbuscular mycorrhizal (AM) fungi and rhizobial bacteria. In both interactions a requirement for successful entry is the activation of a common signalling pathway that includes five genes required to generate calcium oscillations and two genes required for the perception of the calcium response. Recently, it has been discovered that in Medicago truncatula, the Vapyrin (VPY) gene is essential for the establishment of the arbuscular mycorrhizal symbiosis. Here, we show by analyses of mutants that the same gene is also required for rhizobial colonization and nodulation. VPY encodes a protein featuring a Major Sperm Protein domain, typically featured on proteins involved in membrane trafficking and biogenesis, and a series of ankyrin repeats. Plants mutated in this gene have abnormal rhizobial infection threads and fewer nodules, and in the case of interactions with AM fungi, epidermal penetration defects and aborted arbuscule formation. Calcium spiking in root hairs in response to supplied Nod factors is intact in the vpy‐1 mutant. This, and the elevation of VPY transcripts upon application of Nod factors which we show to be dependent on NFP, DMI1, and DMI3, indicates that VPY acts downstream of the common signalling pathway.