Xiaohua Jin

Dr. Xiaohua Jin


Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

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

Representative Publications

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12 July 2016 in Genome Biology and Evolution
Verified
Journal Article
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YFYan-Lei Feng
Yan-Lei Feng
SWSusann Wicke
Susann Wicke
JLJian-Wu Li
Jian-Wu Li
YHYu Han
Yu Han
Choun-sea LinChoun-sea Lin
Choun-sea Lin
XJXiaohua Jin
Xiaohua Jin
The plastid genome (plastome) of heterotrophic plants like mycoheterotrophs and parasites shows massive gene losses in consequence to the relaxation of functional constraints on photosynthesis. To understand the patterns of this convergent plastome reduction syndrome in heterotrophic plants, we studied 12 closely related orchids of three different lifeforms from the tribe Neottieae (Orchidaceae). We employ a comparative genomics approach to examine structural and selectional changes in plastomes within Neottieae. Both leafy and leafless heterotrophic species have functionally reduced plastid genome. Our analyses show that genes for the NAD(P)H dehydrogenase complex, the photosystems, and the RNA polymerase have been lost functionally multiple times independently. The physical reduction proceeds in a highly lineage-specific manner, accompanied by structural reconfigurations such as inversions or modifications of the large inverted repeats. Despite significant but minor selectional changes, all retained genes continue to evolve under purifying selection. All leafless Neottia species, including both visibly green and nongreen members, are fully mycoheterotrophic, likely evolved from leafy and partially mycoheterotrophic species. The plastomes of Neottieae span many stages of plastome degradation, including the longest plastome of a mycoheterotroph, providing invaluable insights into the mechanisms of plastome evolution along the transition from autotrophy to full mycoheterotrophy.

1 October 2019 in Molecular Phylogenetics and Evolution
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Journal Article
Closed access
YLYun-Xia Li
Yun-Xia Li
ZLZhang-Hai Li
Zhang-Hai Li
ASAndre Schuiteman
Andre Schuiteman
MCMark W. Chase
Mark W. Chase
JLJian-Wu Li
Jian-Wu Li
XJXiaohua Jin
Xiaohua Jin

11 April 2015 in BMC Plant Biology
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Journal Article
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TRTracey A Ruhlman
Tracey A Ruhlman
WCWan-Jung Chang
Wan-Jung Chang
JCJeremy Jian Wei Chen
Jeremy Jian Wei Chen
YHYao-Ting Huang
Yao-Ting Huang
MCMing-Tsair Chan
Ming-Tsair Chan
Choun-sea LinChoun-sea Lin
Choun-sea Lin
Key innovations have facilitated novel niche utilization, such as the movement of the algal predecessors of land plants into terrestrial habitats where drastic fluctuations in light intensity, ultraviolet radiation and water limitation required a number of adaptations. The NDH (NADH dehydrogenase-like) complex of Viridiplantae plastids participates in adapting the photosynthetic response to environmental stress, suggesting its involvement in the transition to terrestrial habitats. Although relatively rare, the loss or pseudogenization of plastid NDH genes is widely distributed across diverse lineages of photoautotrophic seed plants and mutants/transgenics lacking NDH function demonstrate little difference from wild type under non-stressed conditions. This study analyzes large transcriptomic and genomic datasets to evaluate the persistence and loss of NDH expression across plants. Nuclear expression profiles showed accretion of the NDH gene complement at key transitions in land plant evolution, such as the transition to land and at the base of the angiosperm lineage. While detection of transcripts for a selection of non-NDH, photosynthesis related proteins was independent of the state of NDH, coordinate, lineage-specific loss of plastid NDH genes and expression of nuclear-encoded NDH subunits was documented in Pinaceae, gnetophytes, Orchidaceae and Geraniales confirming the independent and complete loss of NDH in these diverse seed plant taxa. The broad phylogenetic distribution of NDH loss and the subtle phenotypes of mutants suggest that the NDH complex is of limited biological significance in contemporary plants. While NDH activity appears dispensable under favorable conditions, there were likely sufficiently frequent episodes of abiotic stress affecting terrestrial habitats to allow the retention of NDH activity. These findings reveal genetic factors influencing plant/environment interactions in a changing climate through 450 million years of land plant evolution.

14 February 2016 in Journal of Biogeography
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Journal Article
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XXXiao‐Guo Xiang
Xiao‐Guo Xiang
XMXiang‐Cheng Mi
Xiang‐Cheng Mi
HZHai‐Lang Zhou
Hai‐Lang Zhou
JLJian‐Wu Li
Jian‐Wu Li
SCShih‐Wen Chung
Shih‐Wen Chung
XJXiaohua Jin
Xiaohua Jin

22 June 2021 in Plant Diversity
Verified
Journal Article
Open access
ZZZhihua Zhou
Zhihua Zhou
RSRonghong Shi
Ronghong Shi
YZYu Zhang
Yu Zhang
XXXiaoke Xing
Xiaoke Xing
XJXiaohua Jin
Xiaohua Jin
We review achievements in the conservation of orchid diversity in China over the last 21 years. We provide updated information on orchid biodiversity and suggestions for orchid conservation in China. We outline national policies of biodiversity conservation, especially of orchid conservation, which provide general guidelines for orchid conservation in China. There are now approximately 1708 known species of Orchidaceae in 181 genera in China, including five new genera and 365 new species described over the last 21 years. The assessment of risk of extinction of all 1502 known native orchid species in China in 2013 indicated that 653 species were identified as threatened, 132 species were treated as data-deficient, and four species endemic to China were classified as extinct. Approximately 1100 species (ca. 65%) are protected in national nature reserves, and another ~66 species in provincial nature reserves. About 800 native orchid species have living collections in major botanical gardens. The pollination biology of 74 native orchid species and the genetic diversity and spatial genetic structure of 29 orchid species have been investigated at a local scale and/or across species distributions. The mycorrhizal fungal community composition has been investigated in many genera, such as Bletilla, Coelogyne, Cymbidium, Cypripedium, and Dendrobium. Approximately 292 species will be included in the list of national key protected wild plants this year. Two major tasks for near future include in situ conservation and monitoring population dynamics of endangered species.

20 January 2015 in PLOS ONE
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Journal Article
Open access
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SXSongzhi Xu
Songzhi Xu
DLDe-Zhu Li
De-Zhu Li
JLJianwu Li
Jianwu Li
XXXiaoguo Xiang
Xiaoguo Xiang
WJWeitao Jin
Weitao Jin
LHLuqi Huang
Luqi Huang
DNA barcoding has been proposed to be one of the most promising tools for accurate and rapid identification of taxa. However, few publications have evaluated the efficiency of DNA barcoding for the large genera of flowering plants. Dendrobium, one of the largest genera of flowering plants, contains many species that are important in horticulture, medicine and biodiversity conservation. Besides, Dendrobium is a notoriously difficult group to identify. DNA barcoding was expected to be a supplementary means for species identification, conservation and future studies in Dendrobium. We assessed the power of 11 candidate barcodes on the basis of 1,698 accessions of 184 Dendrobium species obtained primarily from mainland Asia. Our results indicated that five single barcodes, i.e., ITS, ITS2, matK, rbcL and trnH-psbA, can be easily amplified and sequenced with the currently established primers. Four barcodes, ITS, ITS2, ITS+matK, and ITS2+matK, have distinct barcoding gaps. ITS+matK was the optimal barcode based on all evaluation methods. Furthermore, the efficiency of ITS+matK was verified in four other large genera including Ficus, Lysimachia, Paphiopedilum, and Pedicularis in this study. Therefore, we tentatively recommend the combination of ITS+matK as a core DNA barcode for large flowering plant genera.