Tingting Wu

Dr. Tingting Wu


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

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

Representative Publications

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Verified
Journal Article
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ZTZhang Tengfei
Zhang Tengfei
TWTingting Wu
Tingting Wu
LWliwei wang
liwei wang
BJBingjun Jiang
Bingjun Jiang
CZCaixin Zhen
Caixin Zhen
SSShi Sun
Shi Sun
Soybean is an excellent source of vegetable protein and edible oil. Understanding the genetic basis of protein and oil content will improve the breeding programs for soybean. Linkage analysis and genome-wide association study (GWAS) tools were combined to detect quantitative trait loci (QTL) that are associated with protein and oil content in soybean. Three hundred and eight recombinant inbred lines (RILs) containing 3454 single nucleotide polymorphism (SNP) markers and 200 soybean accessions, including 94,462 SNPs and indels, were applied to identify QTL intervals and significant SNP loci. Intervals on chromosomes 1, 15, and 20 were correlated with both traits, and QTL qPro15-1, qPro20-1, and qOil5-1 reproducibly correlated with large phenotypic variations. SNP loci on chromosome 20 that overlapped with qPro20-1 were reproducibly connected to both traits by GWAS (p < 10−4). Twenty-five candidate genes with putative roles in protein and/or oil metabolisms within two regions (qPro15-1, qPro20-1) were identified, and eight of these genes showed differential expressions in parent lines during late reproductive growth stages, consistent with a role in controlling protein and oil content. The new well-defined QTL should significantly improve molecular breeding programs, and the identified candidate genes may help elucidate the mechanisms of protein and oil biosynthesis.

26 May 2017 in BMC Genomics
Verified
Journal Article
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TMTingting Mao
Tingting Mao
ZLZhongqin Luo
Zhongqin Luo
ZWZixiang Wen
Zixiang Wen
TWTingting Wu
Tingting Wu
CWCunxiang Wu
Cunxiang Wu
THTianfu Han
Tianfu Han
Soybean (Glycine max (L.) Merr.) is a short day plant. Its flowering and maturity time are controlled by genetic and environmental factors, as well the interaction between the two factors. Previous studies have shown that both genetic and environmental factors, mainly photoperiod and temperature, control flowering time of soybean. Additionally, these studies have reported gene × gene and gene × environment interactions on flowering time. However, the effects of quantitative trait loci (QTL) in response to photoperiod and temperature have not been well evaluated. The objectives of the current study were to identify the effects of loci associated with flowering time under different photo-thermal conditions and to understand the effects of interaction between loci and environment on soybean flowering. Different photoperiod and temperature combinations were obtained by adjusting sowing dates (spring sowing and summer sowing) or day-length (12 h, 16 h). Association mapping was performed on 91 soybean cultivars from different maturity groups (MG000-VIII) using 172 SSR markers and 5107 SNPs from the Illumina SoySNP6K iSelectBeadChip. The effects of the interaction between QTL and environments on flowering time were also analysed using the QTXNetwork. Large-effect loci were detected on Gm 11, Gm 16 and Gm 20 as in previous reports. Most loci associated with flowering time are sensitive to photo-thermal conditions. Number of loci associated with flowering time was more under the long day (LD) than under the short day (SD) condition. The variation of flowering time among the soybean cultivars mostly resulted from the epistasis × environment and additive × environment interactions. Among the three candidate loci, i.e. Gm04_4497001 (near GmCOL3a), Gm16_30766209 (near GmFT2a and GmFT2b) and Gm19_47514601 (E3 or GmPhyA3), the Gm04_4497001 may be the key locus interacting with other loci for controlling soybean flowering time. The effects of loci associated with the flowering time of soybean were dependent upon the photo-thermal conditions. This study facilitates the understanding of the genetic mechanism of soybean flowering and molecular breeding for the improvement of soybean adaptability to specific and/or broad regions.

19 September 2021 in Agronomy
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Journal Article
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CXCailong Xu
Cailong Xu
RLRuidong Li
Ruidong Li
WSWenwen Song
Wenwen Song
TWTingting Wu
Tingting Wu
SSShi Sun
Shi Sun
CWCunxiang Wu
Cunxiang Wu
Optimizing the spatial distribution of plants under normal conditions of water and fertilizer is widely used by farmers to improve soybean yield. However, the relationship between soybean yield and spatial plant distribution in the field has not been well studied. This study examined the effect of planting density and plant distribution pattern on soybean plant growth, yield components, canopy light interception, and dry matter accumulation. We also analyzed the relationship between photosynthetic rate, dry matter accumulation, and yield under different planting densities and plant distribution. A two year field experiment was conducted during the 2018 and 2019 soybean planting seasons. Two planting densities (1.8 × 105 and 2.7 × 105 plants ha−1) and two plant distribution patterns (uniform and non-uniform plant spacing) were tested. Higher planting density significantly increased the canopy light interception and dry matter accumulation during soybean growth, leading to increased soybean productivity. The seed yield of soybean under higher planting density was 22.8% higher than under normal planting density. Soybean planted under uniform spacing significantly reduced the differences plant-to-plant. Uniform plant spacing significantly increased the canopy light interception and dry matter accumulation of the soybean population. In addition, the coefficient of variation of seed weight per plant between individual plants under uniform plant distribution decreased by 71.5% compared with non-uniform plant distribution. Furthermore, uniform plant distribution increased soybean seed yield by 9.5% over non-uniform plant distribution. This study demonstrates that increasing planting density under uniform plant distribution can be useful to obtain higher seed yield without increasing other farm inputs.

15 January 2021 in Agriculture
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Journal Article
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CXCailong Xu
Cailong Xu
RLRuidong Li
Ruidong Li
WSWenwen Song
Wenwen Song
TWTingting Wu
Tingting Wu
SSShi Sun
Shi Sun
CWCunxiang Wu
Cunxiang Wu
Increasing planting density is one of the key management practices to enhance soybean yield. A 2-yr field experiment was conducted in 2018 and 2019 including six planting densities and two soybean cultivars to determine the effects of planting density on branch number and yield, and analyze the contribution of branches to yield. The yield of ZZXA12938 was 4389 kg ha−1, which was significantly higher than that of ZH13 (+22.4%). In combination with planting year and cultivar, the soybean yield increased significantly by 16.2%, 31.4%, 41.4%, and 46.7% for every increase in density of 45,000 plants ha−1. Yield will not increase when planting density exceeds 315,000 plants ha−1. A correlation analysis showed that pod number per plant increased with the increased branch number, while pod number per unit area decreased; thus, soybean yield decreased. With the increase of branch number, the branch contribution to yield increased first, and then plateaued. ZH13 could produce a high yield under a lower planting density due to more branches, while ZZXA12938 had a higher yield potential under a higher planting density due to the smaller branch number and higher tolerance to close planting. Therefore, seed yield can be increased by selecting cultivars with a little branching capacity under moderately close planting.

20 March 2019 in BMC Genomics
Verified
Journal Article
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BJBingjun Jiang
Bingjun Jiang
SZShouwei Zhang
Shouwei Zhang
WSWenwen Song
Wenwen Song
MKMohammad Abdul Awal Khan
Mohammad Abdul Awal Khan
SSShi Sun
Shi Sun
THTianfu Han
Tianfu Han
Flowering time and maturity are among the most important adaptive traits in soybean (Glycine max (L.) Merill). Flowering Locus T (FT) family genes function as key flowering integrators, with flowering-promoting members GmFT2a/GmFT5a and flowering-inhibiting members GmFT4/GmFT1a antagonistically regulating vegetative and reproductive growth. However, to date, the relations between natural variations of FT family genes and the diversity of flowering time and maturity in soybean are not clear. Therefore, we conducted this study to discover natural variations in FT family genes in association with flowering time and maturity. Ten FT family genes, GmFT1a, GmFT1b, GmFT2a, GmFT2b, GmFT3a, GmFT3b, GmFT4, GmFT5a, GmFT5b and GmFT6, were cloned and sequenced in the 127 varieties evenly covering all 14 known maturity groups (MG0000-MGX). They were diversified at the genome sequence polymorphism level. GmFT3b and GmFT5b might have experienced breeding selection in the process of soybean domestication and breeding. Haplotype analysis showed that a total of 17 haplotypes had correlative relationships with flowering time and maturity among the 10 FT genes, namely, 1a-H3, 1b-H1, 1b-H6, 1b-H7, 2a-H1, 2a-H3, 2a-H4, 2a-H9, 2b-H3, 2b-H4, 2b-H6, 2b-H7, 3b-H4, 5a-H1, 5a-H2, 5a-H4 and 5b-H1. Based on the association analysis, 38 polymorphic sites had a significant association with flowering time at the level of p < 0.01. Some natural variations exist within the 10 FT family genes, which might be involved in soybean adaptation to different environments and have an influence on diverse flowering time and maturity. This study will facilitate the understanding of the roles of FTs in flowering and maturity.

4 May 2021 in Plant Biotechnology Journal
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BJBingjun Jiang
Bingjun Jiang
LCLi Chen
Li Chen
CYChunyan Yang
Chunyan Yang
TWTingting Wu
Tingting Wu
SYShan Yuan
Shan Yuan
SSShi Sun
Shi Sun
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