Jie Wen

Dr. Jie Wen


Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

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

Representative Publications

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1 June 2007 in Poultry Science
Verified
Journal Article
Open access
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QLQ. Lu
Q. Lu
JWJie Wen
Jie Wen
Hongfu ZhangHongfu Zhang
Hongfu Zhang
The effects of chronic heat stress on growth, proportion of carcass and fat deposition, and meat quality were investigated in 2 genetic types of chickens. One hundred and eight 5-wk-old male chickens from a commercially fast-growing strain (Arbor Acres, AA) and a locally slow-growing species (Beijing You chicken, BJY) were kept in the following conditions: constant optimal ambient temperature at 21°C and ad libitum feeding (21AL), constant high ambient temperature at 34°C and ad libitum feeding (34AL), and constant optimal ambient temperature 21°C and pair-fed to the 34AL chickens (21PF). The results showed that feed intakes were decreased by heat exposure in both type of chickens at 8 wk of age (P < 0.001). At 34°C, AA broilers exhibited greatly decreased weight gain (22.38 vs. 61.45 g/d for 21AL) and lower breast proportion compared with 21AL, while the relevant indices of BJY chickens were not affected in hot condition. Abdominal fat deposition of BJY chickens was enhanced by heat exposure (P < 0.05). Fat deposition of AA broilers was decreased in heat-exposed and pair-fed chickens. Abdominal and intermuscular fat deposition in 34AL birds, however, were enhanced compared with 21PF birds (P < 0.01). The L* values, drip loss, initial pH, and shear force of breast meat in BJY chickens were not affected by treatments. In AA birds, chronic heat stress increased L* values and drip loss compared with 21AL, but pH and shear force were not affected by treatments. The results from this study indicated that the impact of heat stress was breed dependent and that BJY chickens showed higher resistance to high ambient temperature, which could be related to their increased feed efficiency and deposition of abdominal fat under heat exposure.

30 May 2012 in BMC Genomics
Verified
Journal Article
Open access
PDF file
HCHuanxian Cui
Huanxian Cui
RLRan-Ran Liu
Ran-Ran Liu
GZGui-Ping Zhao
Gui-Ping Zhao
MZMai-Qing Zheng
Mai-Qing Zheng
Jilan ChenJilan Chen
Jilan Chen
JWJie Wen
Jie Wen
Background: Intramuscular fat (IMF) is one of the important factors influencing meat quality, however, for chickens, the molecular regulatory mechanisms underlying this trait have not yet been determined. In this study, a systematic identification of candidate genes and new pathways related to IMF deposition in chicken breast tissue has been made using gene expression profiles of two distinct breeds: Beijing-you (BJY), a slow-growing Chinese breed possessing high meat quality and Arbor Acres (AA), a commercial fast-growing broiler line. Results: Agilent cDNA microarray analyses were conducted to determine gene expression profiles of breast muscle sampled at different developmental stages of BJY and AA chickens. Relative to d 1 when there is no detectable IMF, breast muscle at d 21, d 42, d 90 and d 120 (only for BJY) contained 1310 differentially expressed genes (DEGs) in BJY and 1080 DEGs in AA. Of these, 34–70 DEGs related to lipid metabolism or muscle development processes were examined further in each breed based on Gene Ontology (GO) analysis. The expression of several DEGs was correlated, positively or negatively, with the changing patterns of lipid content or breast weight across the ages sampled, indicating that those genes may play key roles in these developmental processes. In addition, based on KEGG pathway analysis of DEGs in both BJY and AA chickens, it was found that in addition to pathways affecting lipid metabolism (pathways for MAPK & PPAR signaling), cell junction-related pathways (tight junction, ECM-receptor interaction, focal adhesion, regulation of actin cytoskeleton), which play a prominent role in maintaining the integrity of tissues, could contribute to the IMF deposition. Conclusion: The results of this study identified potential candidate genes associated with chicken IMF deposition and imply that IMF deposition in chicken breast muscle is regulated and mediated not only by genes and pathways related to lipid metabolism and muscle development, but also by others involved in cell junctions. These findings establish the groundwork and provide new clues for deciphering the molecular mechanisms underlying IMF deposition in poultry. Further studies at the translational and posttranslational level are now required to validate the genes and pathways identified here.

18 April 2013 in PLOS ONE
Verified
Journal Article
Open access
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RLRanran Liu
Ranran Liu
YSYanfa Sun
Yanfa Sun
GZGuiping Zhao
Guiping Zhao
FWFangjie Wang
Fangjie Wang
DWDan Wu
Dan Wu
JWJie Wen
Jie Wen
Body composition and meat quality traits are important economic traits of chickens. The development of high-throughput genotyping platforms and relevant statistical methods have enabled genome-wide association studies in chickens. In order to identify molecular markers and candidate genes associated with body composition and meat quality traits, genome-wide association studies were conducted using the Illumina 60 K SNP Beadchip to genotype 724 Beijing-You chickens. For each bird, a total of 16 traits were measured, including carcass weight (CW), eviscerated weight (EW), dressing percentage, breast muscle weight (BrW) and percentage (BrP), thigh muscle weight and percentage, abdominal fat weight and percentage, dry matter and intramuscular fat contents of breast and thigh muscle, ultimate pH, and shear force of the pectoralis major muscle at 100 d of age. The SNPs that were significantly associated with the phenotypic traits were identified using both simple (GLM) and compressed mixed linear (MLM) models. For nine of ten body composition traits studied, SNPs showing genome wide significance (P<2.59E−6) have been identified. A consistent region on chicken (Gallus gallus) chromosome 4 (GGA4), including seven significant SNPs and four candidate genes (LCORL, LAP3, LDB2, TAPT1), were found to be associated with CW and EW. Another 0.65 Mb region on GGA3 for BrW and BrP was identified. After measuring the mRNA content in beast muscle for five genes located in this region, the changes in GJA1 expression were found to be consistent with that of breast muscle weight across development. It is highly possible that GJA1 is a functional gene for breast muscle development in chickens. For meat quality traits, several SNPs reaching suggestive association were identified and possible candidate genes with their functions were discussed.

1 October 2021 in Food Chemistry
Verified
Journal Article
Closed access
YJYuxi Jin
Yuxi Jin
HCHuanxian Cui
Huanxian Cui
XYXiaoya Yuan
Xiaoya Yuan
LLLu Liu
Lu Liu
XLXiaojing Liu
Xiaojing Liu
JWJie Wen
Jie Wen

8 July 2013 in BMC Genomics
Verified
Journal Article
Open access
PDF file
YSYanfa Sun
Yanfa Sun
GZGuiping Zhao
Guiping Zhao
RLRanran Liu
Ranran Liu
MZMaiqing Zheng
Maiqing Zheng
YHYaodong Hu
Yaodong Hu
JWJie Wen
Jie Wen
Background: Meat quality is an important economic trait in chickens. To identify loci and genes associated with meat quality traits, we conducted a genome-wide association study (GWAS) of F2 populations derived from a local Chinese breed (Beijing-You chickens) and a commercial fast-growing broiler line (Cobb-Vantress). Results: In the present study, 33 association signals were detected from the compressed mixed linear model (MLM) for 10 meat quality traits: dry matter in breast muscle (DMBr), dry matter in thigh muscle (DMTh), intramuscular fat content in breast muscle (IMFBr), meat color lightness (L*) and yellowness (b*) values, skin color L*, a* (redness) and b* values, abdominal fat weight (AbFW) and AbFW as a percentage of eviscerated weight (AbFP). Relative expressions of candidate genes identified near significant signals were compared using samples of chickens with High and Low phenotypic values. A total of 14 genes associated with IMFBr, meat color L*, AbFW, and AbFP, were differentially expressed between the High and Low phenotypic groups. These genes are, therefore, prospective candidate genes for meat quality traits: protein tyrosine kinase (TYRO3) and microsomal glutathione S-transferase 1 (MGST1) for IMFBr; collagen, type I, alpha 2 (COL1A2) for meat color L*; and RET proto-oncogene (RET), natriuretic peptide B (NPPB) and sterol regulatory element binding transcription factor 1 (SREBF1) for the abdominal fat (AbF) traits. Conclusions: Based on the association signals and differential expression of nearby genes, 14 candidate loci and genes for IMFBr, meat L* and b* values, and AbF are identified. The results provide new insight into the molecular mechanisms underlying meat quality traits in chickens.

15 November 2019 in BMC Genomics
Verified
Journal Article
Open access
PDF file
LLLu Liu
Lu Liu
XLXiaojing Liu
Xiaojing Liu
HCHuanxian Cui
Huanxian Cui
RLRanran Liu
Ranran Liu
GZGuiping Zhao
Guiping Zhao
JWJie Wen
Jie Wen
Background: Intramuscular fat (IMF) is one of the most important factors positively associated with meat quality. Triglycerides (TGs), as the main component of IMF, play an essential role in muscle lipid metabolism. This transcriptome analysis of pectoralis muscle tissue aimed to identify functional genes and biological pathways likely contributing to the extreme differences in the TG content of broiler chickens.Results: The study included Jingxing-Huang broilers that were significantly different in TG content (5.81 mg/g and 2.26 mg/g,p < 0.01) and deposition of cholesterol also showed the same trend. This RNA sequencing analysis was performed on pectoralis muscle samples from the higher TG content group (HTG) and the lower TG content group (LTG) chickens. A total of 1200 differentially expressed genes (DEGs) were identified between two groups, of which 59 DEGs were related to TG and steroid metabolism. The HTG chickens overexpressed numerous genes related to adipogenesis and lipogenesis in pectoralis muscle tissue, including the key genesADIPOQ,CD36,FABP4,FABP5, LPL,SCD,PLIN1,CIDECandPPARG, as well as genes related to steroid biosynthesis (DHCR24,LSS,MSMO1,NSDHLandCH25H). Additionally, key pathways related to lipid storage and metabolism (the steroid biosynthesis and peroxisome proliferator activated receptor (PPAR) signaling pathway) may be the key pathways regulating differential lipid deposition between HTG group and LTG group.Conclusions: This study showed that increased TG deposition accompanying an increase in steroid synthesis in pectoralis muscle tissue. Our findings of changes in gene expression of steroid biosynthesis and PPAR signaling pathway in HTG and LTG chickens provide insight into genetic mechanisms involved in different lipid deposition patterns in pectoralis muscle tissue.