Xinchun Lin
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Xinchun Lin has a total of 128 co-authors. Here are the top co-authors by number of shared publications:
Dan Hou
State Key Laboratory of Subtropical Silviculture, Zhejiang A&F University, Lin' an 311300, China; Bamboo Industry Institute, Zhejiang A&F University, Lin' an 311300, China
9 shared publicationsShinan Liu
State Key Laboratory of Subtropical Silviculture, Zhejiang Agriculture and Forestry University, Hangzhou 311300, China
8 shared publicationsNaresh Vasupalli
State Key Laboratory of Subtropical Silviculture, Zhejiang A & F University, Lin’an, Hangzhou, Zhejiang, China
6 shared publicationsJuan Zhuo
State Key Laboratory for Development and Utilization of Forest Food Resources, Zhejiang A&F University, Hangzhou, China
5 shared publicationsQiaolu Zang
State Key Laboratory of Subtropical Silviculture, Zhejiang A & F University, Lin'an, 311300, Zhejiang, China
5 shared publicationsTengfei Ma
State Key Laboratory of Subtropical Silviculture, Zhejiang A & F University, Lin’an, Hangzhou, China
5 shared publications
Latest Publications
- 13 October 2026
- Published by Wiley in New Phytologist
PnMYB4a , a R2R3 transcription factor, modulates coumarin biosynthesis during melanization in the culms of Phyllostachys nigra
Summary: Culm colour is one of the primary traits determining the ornamental value of bamboos. The black pigment shown to accumulate in Phyllostachys nigra was previously characterized as melanin, but the underlying regulatory mechanism for its deposition remains elusive. Herein, metabolomics data show that coumarins serve as precursor substrates for melanization in P. nigra , and RNA‐seq and weighted gene correlation network analysis (WGCNA) revealed that the transcription factor PnMYB4a is integral to coumarin biosynthesis. Overexpression of PnMYB4a promotes coumarin production in both Oryza sativa and Arabidopsis thaliana . Pn4CL4‐2 , a biosynthetic gene involved in coumarin biosynthesis, was identified as a direct target gene of PnMYB4a. Additionally, PnWRKY8 and PnWRKY72‐2 were found to interact with PnMYB4a both in vivo and in vitro . Both PnWRKY8 and PnWRKY72‐2 positively promoted coumarin accumulation in transgenic rice, but they repressed the expression of Pn4CL4‐2 by directly binding to W‐box elements within its promoter. Interestingly, PnMYB4a was found to alleviate the inhibitory effect on Pn4CL4‐2 by forming complexes with both PnWRKY8 and PnWRKY72‐2. Collectively, these findings revealed a PnMYB4a‐PnWRKY8/PnWRKY72‐2 regulatory module involved in the coumarin biosynthetic pathway in P. nigra and provide new insights into the mechanisms of melanization and coloration in bamboo species.
- 13 October 2026
- Published by Wiley in New Phytologist
PnMYB4a , a R2R3 transcription factor, modulates coumarin biosynthesis during melanization in the culms of Phyllostachys nigra
Summary: Culm colour is one of the primary traits determining the ornamental value of bamboos. The black pigment shown to accumulate in Phyllostachys nigra was previously characterized as melanin, but the underlying regulatory mechanism for its deposition remains elusive. Herein, metabolomics data show that coumarins serve as precursor substrates for melanization in P. nigra , and RNA‐seq and weighted gene correlation network analysis (WGCNA) revealed that the transcription factor PnMYB4a is integral to coumarin biosynthesis. Overexpression of PnMYB4a promotes coumarin production in both Oryza sativa and Arabidopsis thaliana . Pn4CL4‐2 , a biosynthetic gene involved in coumarin biosynthesis, was identified as a direct target gene of PnMYB4a. Additionally, PnWRKY8 and PnWRKY72‐2 were found to interact with PnMYB4a both in vivo and in vitro . Both PnWRKY8 and PnWRKY72‐2 positively promoted coumarin accumulation in transgenic rice, but they repressed the expression of Pn4CL4‐2 by directly binding to W‐box elements within its promoter. Interestingly, PnMYB4a was found to alleviate the inhibitory effect on Pn4CL4‐2 by forming complexes with both PnWRKY8 and PnWRKY72‐2. Collectively, these findings revealed a PnMYB4a‐PnWRKY8/PnWRKY72‐2 regulatory module involved in the coumarin biosynthetic pathway in P. nigra and provide new insights into the mechanisms of melanization and coloration in bamboo species.
- 14 April 2026
- Published by Springer Nature in Plant Cell, Tissue and Organ Culture (PCTOC)
- Vol. 165 (1) , 28
An efficient embryogenic cell suspension enabling somatic embryogenesis in Phyllostachys edulis
- 14 April 2026
- Published by Springer Nature in Plant Cell, Tissue and Organ Culture (PCTOC)
- Vol. 165 (1) , 28
An efficient embryogenic cell suspension enabling somatic embryogenesis in Phyllostachys edulis
- 21 January 2026
- Published by Springer Nature in Plant Molecular Biology
- Vol. 116 (1) , 10
Flowering time regulation: a critical review focusing on FKF1 protein
- 21 January 2026
- Published by Springer Nature in Plant Molecular Biology
- Vol. 116 (1) , 10
Flowering time regulation: a critical review focusing on FKF1 protein
- Open Access
- 1 September 2025
- Published by Springer Nature in BMC Plant Biology
- Vol. 25 (1) , 1-15
Chloroplast genome analysis of Dendrocalamus × mutatus and its implications for bamboo classification
Background: The bamboo species Dendrocalamus × mutatus T.P.Yi & B.X.Li (D. mutatus) holds great economic and ecological importance in China. Although previously D. mutatus was presumed to be a hybrid of Bambusa grandis and Bambusa pervariabilis, its taxonomic status has remained uncertain. Therefore, we combined plastomes and nuclear SSR datasets, in addition to morphological data, to refine our understanding of the taxonomic status of D. mutatus. Results: The chloroplast genome of D. mutatus exhibits a typical quadripartite structure, comprising a large single-copy region (LSC), a small single-copy region (SSC), and two inverted repeat regions (IRa and IRb), containing a total length of 139,432 bp. Comparative genomic analyses revealed extremely high similarity between D. mutatus and D. yunnanicus, differing by only two single-nucleotide polymorphisms (SNPs). In contrast, a greater divergence was observed when compared with D. sikkimensis (six SNPs and one four-base insertion). Phylogenetic reconstruction using the Maximum Likelihood and Bayesian Inference method based on chloroplast genomes strongly supported the close relationship between D. mutatus and D. yunnanicus, while distinctly separating them from the previously proposed parent species Bambusa grandis and Bambusa pervariabilis. Morphological comparisons further confirmed the similarity between D. mutatus and D. yunnanicus, particularly with respect to the absence of conspicuous culm sheath auricles and oral setae, as well as the lack of fimbriate hairs on the ligule. Nuclear SSR marker analyses also showed identical predominant allele at the SSR 23 and 24 loci between D. mutatus and D. yunnanicus. Collectively, the comprehensive integration of chloroplast genome data, nuclear SSR evidence, and morphological observations supports the conclusion that D. mutatus is a synonym of D. yunnanicus rather than a hybrid of Bambusa grandis and Bambusa pervariabilis. Conclusions: This research provides a comprehensive understanding of the chloroplast genome of D. mutatus, providing valuable insights that enhance the taxonomic resolution and conservation strategies for bamboo species.
- 1 September 2025
- Published by Springer Nature in BMC Plant Biology
- Vol. 25 (1) , 1-15
Open AccessChloroplast genome analysis of Dendrocalamus × mutatus and its implications for bamboo classification
Background: The bamboo species Dendrocalamus × mutatus T.P.Yi & B.X.Li (D. mutatus) holds great economic and ecological importance in China. Although previously D. mutatus was presumed to be a hybrid of Bambusa grandis and Bambusa pervariabilis, its taxonomic status has remained uncertain. Therefore, we combined plastomes and nuclear SSR datasets, in addition to morphological data, to refine our understanding of the taxonomic status of D. mutatus. Results: The chloroplast genome of D. mutatus exhibits a typical quadripartite structure, comprising a large single-copy region (LSC), a small single-copy region (SSC), and two inverted repeat regions (IRa and IRb), containing a total length of 139,432 bp. Comparative genomic analyses revealed extremely high similarity between D. mutatus and D. yunnanicus, differing by only two single-nucleotide polymorphisms (SNPs). In contrast, a greater divergence was observed when compared with D. sikkimensis (six SNPs and one four-base insertion). Phylogenetic reconstruction using the Maximum Likelihood and Bayesian Inference method based on chloroplast genomes strongly supported the close relationship between D. mutatus and D. yunnanicus, while distinctly separating them from the previously proposed parent species Bambusa grandis and Bambusa pervariabilis. Morphological comparisons further confirmed the similarity between D. mutatus and D. yunnanicus, particularly with respect to the absence of conspicuous culm sheath auricles and oral setae, as well as the lack of fimbriate hairs on the ligule. Nuclear SSR marker analyses also showed identical predominant allele at the SSR 23 and 24 loci between D. mutatus and D. yunnanicus. Collectively, the comprehensive integration of chloroplast genome data, nuclear SSR evidence, and morphological observations supports the conclusion that D. mutatus is a synonym of D. yunnanicus rather than a hybrid of Bambusa grandis and Bambusa pervariabilis. Conclusions: This research provides a comprehensive understanding of the chloroplast genome of D. mutatus, providing valuable insights that enhance the taxonomic resolution and conservation strategies for bamboo species.
- Open Access
- 5 February 2025
- Published by Frontiers Media SA in Frontiers in Plant Science
- Vol. 16, 1540693
Advances in plant male sterility for hybrid seed production: an overview of conditional nuclear male sterile lines and biotechnology-based male sterile systems
Male sterility forms the foundation of hybrid seed production technology in field crops. A variety of genetically controlled male sterility/fertility systems starting with cytoplasmic male sterility (CMS), genic male sterility (GMS) including conditional male sterility and transgenic-based male sterility have been developed and deployed for heterosis breeding over the past century. Here we review environment-sensitive genic male sterility (EGMS) and biotechnology-based male sterility systems and describe the underlying molecular mechanisms. Advances in crop genomics and discovery of a large number of nuclear genes governing anther/pollen development, which are shared across species, are helping design diverse types of male sterile lines suitable for different crop species and situations. In particular, gene editing offers quick and easy route to develop novel male sterility systems for hybrid seed production. We discuss the advantages and challenges of biotechnology-based male sterility systems and present alternative strategies to address concerns of transgenics. Finally, we propose development of functional male sterility systems based on pollen competition as the future area that holds great promise for heterosis breeding.
- 5 February 2025
- Published by Frontiers Media SA in Frontiers in Plant Science
- Vol. 16, 1540693
Open AccessAdvances in plant male sterility for hybrid seed production: an overview of conditional nuclear male sterile lines and biotechnology-based male sterile systems
Male sterility forms the foundation of hybrid seed production technology in field crops. A variety of genetically controlled male sterility/fertility systems starting with cytoplasmic male sterility (CMS), genic male sterility (GMS) including conditional male sterility and transgenic-based male sterility have been developed and deployed for heterosis breeding over the past century. Here we review environment-sensitive genic male sterility (EGMS) and biotechnology-based male sterility systems and describe the underlying molecular mechanisms. Advances in crop genomics and discovery of a large number of nuclear genes governing anther/pollen development, which are shared across species, are helping design diverse types of male sterile lines suitable for different crop species and situations. In particular, gene editing offers quick and easy route to develop novel male sterility systems for hybrid seed production. We discuss the advantages and challenges of biotechnology-based male sterility systems and present alternative strategies to address concerns of transgenics. Finally, we propose development of functional male sterility systems based on pollen competition as the future area that holds great promise for heterosis breeding.
- Open Access
- 1 January 2025
- Published by Maximum Academic Press in Forestry Research
- Vol. 5 (1) , e020
Integrative transcriptome and metabolome evaluation of melanin biosynthesis in Phyllostachys nigra during low-temperature growth
Plant melanin is an organic molecule commonly used in medicine, food, and chemical industries. However, the molecular underpinnings of plant melanin's biosynthesis and its regulation are still unclear. Phyllostachys nigra is well known for its ornamental value because of its black culms. The black pigments enriched in the epidermis and cortex of P. nigra were identified to be melanin by analyses of its physical and chemical properties. Moreover, the biosynthesis of melanin was examined using comprehensive transcriptomic and metabolomic analyses in P. nigra when grown at low temperatures. Nontargeted metabolite profiling revealed that some indoles, including serotonin, 3-indoleacetic acid, and 1H-indole-3-acetamide, were significantly enriched in P. nigra when grown at low temperatures. Parallel transcriptomic analysis showed that a set of structural genes involved in serotonin biosynthesis was significantly upregulated by low temperatures. By integrating the transcriptome data and weighted gene co-expression network analysis, the essential transcription factors that putatively regulate the biosynthesis of serotonins were revealed. Among those, PnWRKY19-3 was functionally tested and shown to increase the serotonin content in transgenic rice by upregulating OsT5H under low temperature conditions. These findings suggest that PnWRKY19-3 may play a positive role in promoting melanin formation in the culms of P. nigra. According to the two functional genomic platforms, it appears that low temperature stimulates melanin formation in P. nigra by inducing the biosynthesis of indoles. Our research provides new insights into melanin biosynthesis in bamboo, which may be vital to other plant species.
- 1 January 2025
- Published by Maximum Academic Press in Forestry Research
- Vol. 5 (1) , e020
Open AccessIntegrative transcriptome and metabolome evaluation of melanin biosynthesis in Phyllostachys nigra during low-temperature growth
Plant melanin is an organic molecule commonly used in medicine, food, and chemical industries. However, the molecular underpinnings of plant melanin's biosynthesis and its regulation are still unclear. Phyllostachys nigra is well known for its ornamental value because of its black culms. The black pigments enriched in the epidermis and cortex of P. nigra were identified to be melanin by analyses of its physical and chemical properties. Moreover, the biosynthesis of melanin was examined using comprehensive transcriptomic and metabolomic analyses in P. nigra when grown at low temperatures. Nontargeted metabolite profiling revealed that some indoles, including serotonin, 3-indoleacetic acid, and 1H-indole-3-acetamide, were significantly enriched in P. nigra when grown at low temperatures. Parallel transcriptomic analysis showed that a set of structural genes involved in serotonin biosynthesis was significantly upregulated by low temperatures. By integrating the transcriptome data and weighted gene co-expression network analysis, the essential transcription factors that putatively regulate the biosynthesis of serotonins were revealed. Among those, PnWRKY19-3 was functionally tested and shown to increase the serotonin content in transgenic rice by upregulating OsT5H under low temperature conditions. These findings suggest that PnWRKY19-3 may play a positive role in promoting melanin formation in the culms of P. nigra. According to the two functional genomic platforms, it appears that low temperature stimulates melanin formation in P. nigra by inducing the biosynthesis of indoles. Our research provides new insights into melanin biosynthesis in bamboo, which may be vital to other plant species.
- 7 December 2024
- Published by Elsevier in Plant Physiology and Biochemistry
- Vol. 219, 109392
Evolutionary analysis of CBFs/DREB1s in temperate and tropical woody bamboos and functional study of PeDREB1A3 under cold and drought stress
- 7 December 2024
- Published by Elsevier in Plant Physiology and Biochemistry
- Vol. 219, 109392
Evolutionary analysis of CBFs/DREB1s in temperate and tropical woody bamboos and functional study of PeDREB1A3 under cold and drought stress
- 14 November 2024
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 283 (Pt 1) , 137593
F-box protein PeFKF1 promotes flowering by cooperating with PeID1 and PeHd1 in Phyllostachys edulis
- 14 November 2024
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 283 (Pt 1) , 137593
F-box protein PeFKF1 promotes flowering by cooperating with PeID1 and PeHd1 in Phyllostachys edulis
- Open Access
- 1 September 2023
- Published by Frontiers Media SA in Frontiers in Plant Science
- Vol. 14, 1231940
Molecular identification of Bambusa changningensis is the natural bamboo hybrid of B. rigida × Dendrocalamus farinosus
Bamboo is one of the fastest-growing plants commonly used in food, fibre, paper, biofuel, ornamental and medicinal industries. Natural hybridization in bamboo is rare due to its long vegetative period followed by gregarious flowering and death of the entire population. In the current study, a new bamboo species, Bambusa changningensis, shows intermediate characteristics of Dendrocalamus farinosus and B. rigida morphologically, but it is unknown whether B. changningensis is a natural hybrid. Moreover, B. changningensis has been identified as a superior variety of Sichuan Province with high pulping yield, fibre length and width. Therefore, we analyzed the morphological characteristics, DNA markers, DNA barcoding and chloroplast genomes to identify the hybrid origin of B. changningensis and possible maternal parent. We have developed the transcriptomic data for B. changningensis and mined the SSR loci. The putative parental lines and hybrid were screened for 64 SSR makers and identified that SSR14, SSR28, SSR31 and SSR34 markers showed both alleles of the parental species in B. changningensis, proving heterozygosity. Sequencing nuclear gene GBSSI partial regions and phylogenetic analysis also confirm the hybrid nature of B. changningensis. Further, we have generated the complete chloroplast genome sequence (139505 bp) of B. changningensis. By analyzing the cp genomes of both parents and B. changningensis, we identified that B. rigida might be the female parent. In conclusion, our study identified that B. changningensis is a natural hybrid, providing evidence for bamboo’s natural hybridization. This is the first report on confirming a natural bamboo hybrid and its parents through SSR and chloroplast genome sequence.
- 1 September 2023
- Published by Frontiers Media SA in Frontiers in Plant Science
- Vol. 14, 1231940
Open AccessMolecular identification of Bambusa changningensis is the natural bamboo hybrid of B. rigida × Dendrocalamus farinosus
Bamboo is one of the fastest-growing plants commonly used in food, fibre, paper, biofuel, ornamental and medicinal industries. Natural hybridization in bamboo is rare due to its long vegetative period followed by gregarious flowering and death of the entire population. In the current study, a new bamboo species, Bambusa changningensis, shows intermediate characteristics of Dendrocalamus farinosus and B. rigida morphologically, but it is unknown whether B. changningensis is a natural hybrid. Moreover, B. changningensis has been identified as a superior variety of Sichuan Province with high pulping yield, fibre length and width. Therefore, we analyzed the morphological characteristics, DNA markers, DNA barcoding and chloroplast genomes to identify the hybrid origin of B. changningensis and possible maternal parent. We have developed the transcriptomic data for B. changningensis and mined the SSR loci. The putative parental lines and hybrid were screened for 64 SSR makers and identified that SSR14, SSR28, SSR31 and SSR34 markers showed both alleles of the parental species in B. changningensis, proving heterozygosity. Sequencing nuclear gene GBSSI partial regions and phylogenetic analysis also confirm the hybrid nature of B. changningensis. Further, we have generated the complete chloroplast genome sequence (139505 bp) of B. changningensis. By analyzing the cp genomes of both parents and B. changningensis, we identified that B. rigida might be the female parent. In conclusion, our study identified that B. changningensis is a natural hybrid, providing evidence for bamboo’s natural hybridization. This is the first report on confirming a natural bamboo hybrid and its parents through SSR and chloroplast genome sequence.
- Open Access
Identification of Structural Differentiation and Differentially Expressed Genes between Sulcus and Culm of Phyllostachys violascens cv. Viridisulcata
Bamboo is one of the essential ornamental plants that is widely used as a decorative landscape element in gardens. Phyllostachys violascens cv. Viridisulcata has a unique internode color phenotype with yellow culm and green sulcus, but their structural and development differences remain unknown. In the current study, we analyzed the histological analysis of internode cross-sections through SEM and microscopy. These results revealed that the vascular bundles distributed in the culm were organized in oblique rows and multiple lines. In contrast, the vascular bundles’ distribution in the sulcus was much more random. The distribution density, maximum length, and maximum width of vascular bundles were also differentiated between the sulcus and the culm. Further, the cell wall thickness of fiber cells in the culm was more than 30% thicker than the sulcus. The FT-IR analysis identified that the culm and sulcus had similar structural properties. The total lignin content measurement revealed that lignin accumulated more in the sulcus than in the culm. Additionally, we identified the lignin biosynthesis pathway genes, Pv4CL and PvC4H, which were differentially expressed between the culm and sulcus through transcriptomic data and qPCR analyses. In conclusion, our results identified that the vascular bundles’ structure differed between the culm and sulcus, and Pv4CL and PvC4H genes might play an essential role in their development.
Open AccessIdentification of Structural Differentiation and Differentially Expressed Genes between Sulcus and Culm of Phyllostachys violascens cv. Viridisulcata
Bamboo is one of the essential ornamental plants that is widely used as a decorative landscape element in gardens. Phyllostachys violascens cv. Viridisulcata has a unique internode color phenotype with yellow culm and green sulcus, but their structural and development differences remain unknown. In the current study, we analyzed the histological analysis of internode cross-sections through SEM and microscopy. These results revealed that the vascular bundles distributed in the culm were organized in oblique rows and multiple lines. In contrast, the vascular bundles’ distribution in the sulcus was much more random. The distribution density, maximum length, and maximum width of vascular bundles were also differentiated between the sulcus and the culm. Further, the cell wall thickness of fiber cells in the culm was more than 30% thicker than the sulcus. The FT-IR analysis identified that the culm and sulcus had similar structural properties. The total lignin content measurement revealed that lignin accumulated more in the sulcus than in the culm. Additionally, we identified the lignin biosynthesis pathway genes, Pv4CL and PvC4H, which were differentially expressed between the culm and sulcus through transcriptomic data and qPCR analyses. In conclusion, our results identified that the vascular bundles’ structure differed between the culm and sulcus, and Pv4CL and PvC4H genes might play an essential role in their development.