Junkang Rong

Dr. Junkang Rong

Zhejiang A & F University, Lin’an, China

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

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13 June 2012 in BMC Plant Biology
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Journal Article
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ACAiqun Chen
Aiqun Chen
SHShae He
Shae He
FLFeifei Li
Feifei Li
ZLZhao Li
Zhao Li
RJRong Junkang
Rong Junkang
JRJunkang Rong
Junkang Rong
Background: In plants, sucrose synthase (Sus) is widely considered as a key enzyme involved in sucrose metabolism. Several paralogous genes encoding different isozymes of Sus have been identified and characterized in multiple plant genomes, while limited information of Sus genes is available to date for cotton. Results: Here, we report the molecular cloning, structural organization, phylogenetic evolution and expression profiles of seven Sus genes (GaSus1 to 7) identified from diploid fiber cotton (Gossypium arboreum). Comparisons between cDNA and genomic sequences revealed that the cotton GaSus genes were interrupted by multiple introns. Comparative screening of introns in homologous genes demonstrated that the number and position of Sus introns are highly conserved among Sus genes in cotton and other more distantly related plant species. Phylogenetic analysis showed that GaSus1, GaSus2, GaSus3, GaSus4 and GaSus5 could be clustered together into a dicot Sus group, while GaSus6 and GaSus7 were separated evenly into other two groups, with members from both dicot and monocot species. Expression profiles analyses of the seven Sus genes indicated that except GaSus2, of which the transcripts was undetectable in all tissues examined, and GaSus7, which was only expressed in stem and petal, the other five paralogues were differentially expressed in a wide ranges of tissues, and showed development-dependent expression profiles in cotton fiber cells. Conclusions: This is a comprehensive study of the Sus gene family in cotton plant. The results presented in this work provide new insights into the evolutionary conservation and sub-functional divergence of the cotton Sus gene family in response to cotton fiber growth and development.

5 September 2014 in Molecular Genetics and Genomics
Verified
Journal Article
Closed access
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MDMingquan Ding
Mingquan Ding
JCJiadong Chen
Jiadong Chen
YJYurong Jiang
Yurong Jiang
LLLifeng Lin
Lifeng Lin
YCYueFen Cao
YueFen Cao
Wuwei YeWuwei Ye
Wuwei Ye

1 February 2014 in Gene
Verified
Journal Article
Closed access
MDMingquan Ding
Mingquan Ding
YJYurong Jiang
Yurong Jiang
YCYuefen Cao
Yuefen Cao
LLLifeng Lin
Lifeng Lin
SHShae He
Shae He
JRJunkang Rong
Junkang Rong

22 June 2010 in BMC Genomics
Verified
Journal Article
Open access
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LLLifeng Lin
Lifeng Lin
GPGary J Pierce
Gary J Pierce
JBJohn Bowers
John Bowers
JEJames C Estill
James C Estill
RCRosana O Compton
Rosana O Compton
APAndrew Paterson
Andrew Paterson
Genetically anchored physical maps of large eukaryotic genomes have proven useful both for their intrinsic merit and as an adjunct to genome sequencing. Cultivated tetraploid cottons, Gossypium hirsutum and G. barbadense, share a common ancestor formed by a merger of the A and D genomes about 1-2 million years ago. Toward the long-term goal of characterizing the spectrum of diversity among cotton genomes, the worldwide cotton community has prioritized the D genome progenitor Gossypium raimondii for complete sequencing. A whole genome physical map of G. raimondii, the putative D genome ancestral species of tetraploid cottons was assembled, integrating genetically-anchored overgo hybridization probes, agarose based fingerprints and 'high information content fingerprinting' (HICF). A total of 13,662 BAC-end sequences and 2,828 DNA probes were used in genetically anchoring 1585 contigs to a cotton consensus genetic map, and 370 and 438 contigs, respectively to Arabidopsis thaliana (AT) and Vitis vinifera (VV) whole genome sequences. Several lines of evidence suggest that the G. raimondii genome is comprised of two qualitatively different components. Much of the gene rich component is aligned to the Arabidopsis and Vitis vinifera genomes and shows promise for utilizing translational genomic approaches in understanding this important genome and its resident genes. The integrated genetic-physical map is of value both in assembling and validating a planned reference sequence.

9 June 2025 in Nature Genetics
Verified
Journal Article
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ZKZhu Keyu
Zhu Keyu
MLMiaomiao Li
Miaomiao Li
LDLingli Dong
Lingli Dong
HZHuaizhi Zhang
Huaizhi Zhang
DZDeyun Zhang
Deyun Zhang
ZLZhiyong Liu
Zhiyong Liu

1 July 2015 in Genetics
Verified
Journal Article
Open access
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MDMingquan Ding
Mingquan Ding
WYWuwei Ye
Wuwei Ye
LLLifeng Lin
Lifeng Lin
SHShae He
Shae He
XDXiongming Du
Xiongming Du
JRJunkang Rong
Junkang Rong
Cotton (Gossypium) stem trichomes are mostly single cells that arise from stem epidermal cells. In this study, a homeodomain-leucine zipper gene (HD1) was found to cosegregate with the dominant trichome locus previously designated as T1 and mapped to chromosome 6. Characterization of HD1 orthologs revealed that the absence of stem trichomes in modern Gossypium barbadense varieties is linked to a large retrotransposon insertion in the ninth exon, 2565 bp downstream from the initial codon in the At subgenome HD1 gene (At-GbHD1). In both the At and Dt subgenomes, reduced transcription of GbHD1 genes is caused by this insertion. The disruption of At-HD1 further affects the expression of downstream GbMYB25 and GbHOX3 genes. Analyses of primitive cultivated accessions identified another retrotransposon insertion event in the sixth exon of At-GbHD1 that might predate the previously identified retrotransposon in modern varieties. Although both retrotransposon insertions results in similar phenotypic changes, the timing of these two retrotransposon insertion events fits well with our current understanding of the history of cotton speciation and dispersal. Taken together, the results of genetics mapping, gene expression and association analyses suggest that GbHD1 is an important component that controls stem trichome development and is a promising candidate gene for the T1 locus. The interspecific phenotypic difference in stem trichome traits also may be attributable to HD1 inactivation associated with retrotransposon insertion.