Summary of Study ST001112

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR000743. The data can be accessed directly via it's Project DOI: 10.21228/M8N68W This work is supported by NIH grant, U2C- DK119886.

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Study IDST001112
Study TitleThe nutrition value of fish fillet is related to fish maturation or fish age?
Study Summary Integrated analysis of transcriptomics and metabolomics in Blunt Snout Bream. With the improvement of living standards, people’s demand for food nutrient is getting higher and higher. Fish is one kind of protein-rich food and is increasingly favored by consumers. It has been well recognized that flesh composition of fish is closely related to its maturation and growth stages, but few researches have explored these differences. Besides, hormone residues in fish after artificial inducing reproduction also attract consumers’ concern. In this study, we try to address these concerns by using a combination of transcriptomics and metabolomics analysis to identify the key pathways, genes, and metabolites regulation which may affect flesh nutrition of one typical aquaculture species in China, blunt snout bream (Megalobrama amblycephala).
Institute
Huazhong Agricultural University
Last NameGuan
First NameNingnan
AddressCollege of Fisheries,Huazhong Agricultural University 1 Shizishan Road Hongshan District Wuhan, Hubei
Emailningnan06@163.com
Phone+8613007100773
Submit Date2017-09-19
Raw Data AvailableYes
Raw Data File Type(s)bcd
Analysis Type DetailLC-MS
Release Date2019-01-22
Release Version1
Ningnan Guan Ningnan Guan
https://dx.doi.org/10.21228/M8N68W
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR000743
Project DOI:doi: 10.21228/M8N68W
Project Title:The nutrition value of fish fillet is related to fish maturation or fish age
Project Type:metabolomic
Project Summary:With the improvement of living standards, people’s demand for food nutrient is getting higher and higher. Fish is one kind of protein-rich food and is increasingly favored by consumers. It has been well recognized that flesh composition of fish is closely related to its maturation and growth stages, but few researches have explored these differences. Besides, hormone residues in fish after artificial inducing reproduction also attract consumers’ concern. In this study, we try to address these concerns by using a combination of transcriptomics and metabolomics analysis to identify the key pathways, genes, and metabolites regulation which may affect flesh nutrition of one typical aquaculture species in China, blunt snout bream (Megalobrama amblycephala).
Institute:Huazhong Agricultural University
Department:Breeding and Reproduction of Ministry of Education
Laboratory:Key Laboratory of Agricultural Animal Genetics
Last Name:Guan
First Name:Ningnan
Address:College of Fisheries,Huazhong Agricultural University 1 Shizishan Road Hongshan District Wuhan, Hubei
Email:ningnan06@163.com
Phone:+8613007100773
Funding Source:National Natural Science Foundation of China
Project Comments:none
Publications:none
Contributors:Shiming-Wan, Bowen-Zhao, Laifang-Zhou, Weizhuo-Zhang

Subject:

Subject ID:SU001157
Subject Type:Fish
Subject Species:Megalobrama amblycephala
Taxonomy ID:75352

Factors:

Subject type: Fish; Subject species: Megalobrama amblycephala (Factor headings shown in green)

mb_sample_id local_sample_id age(years) mature spawned hormone treatment
SA075861M-GroupI_231 No No Yes
SA075862M-GroupI_191 No No Yes
SA075863M-GroupI_141 No No Yes
SA075864M-GroupI_281 No No Yes
SA075865M-GroupI_361 No No Yes
SA075866M-GroupI_451 No No Yes
SA075867M-GroupI_411 No No Yes
SA075868M-GroupI_101 No No Yes
SA075869M-GroupI_321 No No Yes
SA075870M-GroupI_61 No No Yes
SA075871M-GroupII_202 No No Yes
SA075872M-GroupII_152 No No Yes
SA075873M-GroupII_112 No No Yes
SA075874M-GroupII_72 No No Yes
SA075875M-GroupII_292 No No Yes
SA075876M-GroupII_242 No No Yes
SA075877M-GroupII_332 No No Yes
SA075878M-GroupII_422 No No Yes
SA075879M-GroupII_462 No No Yes
SA075880M-GroupII_372 No No Yes
SA075881M-GroupIII_252 Yes No No
SA075882M-GroupIII_212 Yes No No
SA075883M-GroupIII_122 Yes No No
SA075884M-GroupIII_302 Yes No No
SA075885M-GroupIII_172 Yes No No
SA075886M-GroupIII_342 Yes No No
SA075887M-GroupIII_82 Yes No No
SA075888M-GroupIII_472 Yes No No
SA075889M-GroupIII_432 Yes No No
SA075890M-GroupIII_392 Yes No No
SA075891M-GroupIV_312 Yes Yes Yes
SA075892M-GroupIV_262 Yes Yes Yes
SA075893M-GroupIV_182 Yes Yes Yes
SA075894M-GroupIV_352 Yes Yes Yes
SA075895M-GroupIV_222 Yes Yes Yes
SA075896M-GroupIV_482 Yes Yes Yes
SA075897M-GroupIV_92 Yes Yes Yes
SA075898M-GroupIV_132 Yes Yes Yes
SA075899M-GroupIV_442 Yes Yes Yes
SA075900M-GroupIV_402 Yes Yes Yes
Showing results 1 to 40 of 40

Collection:

Collection ID:CO001151
Collection Summary:The gonads of fish were collected to identify its sex of 1-year-old fish by traditional histological analysis and the muscle samples were only selected from the females (group Ⅰ). As to 2-year-old M. amblycephala, the muscle samples were firstly collected from individuals, and then the gonads were collected to do the histological analysis. Individuals with ovary development before stage Ⅴ were recognized as non-mature females (group Ⅱ), while individuals with ovary development at stage Ⅴdwere recognized as mature females (group ⅡI). For group IV, the individuals which normally spawned during artificial reproduction, were put back to tank and then muscle samples were collected after 24 hours. For each group, muscle samples from 10 individuals were collected. After the collection, muscle samples were frozen in liquid nitrogen immediately and then transferred them into -80℃ for further study.
Sample Type:Muscle and Gonad tissue

Treatment:

Treatment ID:TR001171
Treatment Summary:Samples were divided into four groups: 1-year-old immature M. amblycephala females (group Ⅰ), 2-year-old immature M. amblycephala females (group Ⅰ), 2-year-old mature females before the injection of hormones (group Ⅲ) and 2-year-old females after 24 hours of their successfully spawning by injecting oxytocin (group ⅣanThe artificial oxytocin implementation procedure was as follows. Firstly, the fish were intraperitoneally injected with a luteinizing hormone-releasing hormone from the basal part of the pectoral fin (LRH-A2) (1 µg/kg fish body weight). After 10 h, the second injection was given (0.5 ml/kg body weight) (each ml contained LRH-A2 4 µg, human chorionic gonadotropin (HCG) 500 U, and domperidone (DOM) 5 mg of solution).

Sample Preparation:

Sampleprep ID:SP001164
Sampleprep Summary:Muscle tissues about 25 mg from each individual were homogenized in 800 µL cold methanol and water (v/v = 1:1) using a Qiagen Tissue-Lyser (Retsch GmBH, Germany). 400 µL supernatant was collected after centrifugation (25000 g, 4 °C, 10 min). The supernatant in the eppendorf tube was removed and the sediment in the tube was dried. Homogenized the sediment again in 800 µL cold dichloromethane and methanol (v/v = 3:1), after centrifuging and then collected 200 µL supernatant for QC (quality control) sample (25000 g, 4 °C, 10 min). The supernatant was evacuated under vacuum, re-collected 100µL supernatant after centrifugation (25000 g, 4 °C, 10 min) for subsequent detection.

Combined analysis:

Analysis ID AN001807 AN001808
Analysis type MS MS
Chromatography type Unspecified Unspecified
Chromatography system Waters Waters
Column ion information ion information
MS Type ESI ESI
MS instrument type QTOF QTOF
MS instrument name Waters Synapt G2 XS Waters Synapt G2 XS
Ion Mode POSITIVE NEGATIVE
Units none none

Chromatography:

Chromatography ID:CH001273
Instrument Name:Waters
Column Name:ion information
Chromatography Type:Unspecified

MS:

MS ID:MS001665
Analysis ID:AN001807
Instrument Name:Waters Synapt G2 XS
Instrument Type:QTOF
MS Type:ESI
Ion Mode:POSITIVE
  
MS ID:MS001666
Analysis ID:AN001808
Instrument Name:Waters Synapt G2 XS
Instrument Type:QTOF
MS Type:ESI
Ion Mode:NEGATIVE
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