Home
/
Search
/
Gene
RNA
Bioproject
Expression
/
Analysis
/
Coding ability prediction
Expression count
Visual Omics
Tools
/
Neighbor
BLAST
Statistics
/
Download
/
Help
Examples.
×
EXAMPLES:
gene
XLOC_000007
f7
RNA
TCONS_00000019
bioproject
PRJEB12982
bowfin
(
Amia calva
)
eurasian perch
(
Perca fluviatilis
)
grass carp
(
Ctenopharyngodon idella
)
mexican tetra
(
Astyanax mexicanus
)
rainbow trout
(
Oncorhynchus mykiss
)
striped catfish
(
Pangasianodon hypophthalmus
)
tiger barb
(
Puntius tetrazona
)
zebrafish
(
Danio rerio
)
simplified version
bowfin
(
Amia calva
)
eurasian perch
(
Perca fluviatilis
)
grass carp
(
Ctenopharyngodon idella
)
mexican tetra
(
Astyanax mexicanus
)
rainbow trout
(
Oncorhynchus mykiss
)
striped catfish
(
Pangasianodon hypophthalmus
)
tiger barb
(
Puntius tetrazona
)
zebrafish
(
Danio rerio
)
simplified version
Bioproject
Please select the
sample of bioproject
for visualization of expression.
Click on the
node of the fold tree
to expand the information about the bioproject and sample.
Check the sample
checkbox
for sample selection.
baseline
PRJNA684636
:
We performed the genome sequencing of Puntius tetrazona using Nanopore, Illumina and HiC technologies and generate a chromosome-level assembly. Using transcriptome sequencing from multiple tissues, we predicted protein-coding genes of this species.
key word
baseline;GENETIC DIVERSITY;PROVIDES INSIGHTS;MODEL SELECTION;GENOME SEQUENCE;READ ALIGNMENT;POLYPLOIDY;ORIGIN;ANNOTATION;RECONSTRUCTION;FRACTIONATION
publication
Jiong-Tang, L. , et al. "Parallel subgenome structure and divergent expression evolution of allo-tetraploid common carp and goldfish." Nature Genetics.
abstract
Genomic analysis of allo-tetraploid common carp and goldfish identifies parallel subgenome structure and divergent expression processes. How two subgenomes in allo-tetraploids adapt to coexistence and coordinate through structure and expression evolution requires extensive studies. In the present study, we report an improved genome assembly of allo-tetraploid common carp, an updated genome annotation of allo-tetraploid goldfish and the chromosome-scale assemblies of a progenitor-like diploid Puntius tetrazona and an outgroup diploid Paracanthobrama guichenoti. Parallel subgenome structure evolution in the allo-tetraploids was featured with equivalent chromosome components, higher protein identities, similar transposon divergence and contents, homoeologous exchanges, better synteny level, strong sequence compensation and symmetric purifying selection. Furthermore, we observed subgenome expression divergence processes in the allo-tetraploids, including inter-/intrasubgenome trans-splicing events, expression dominance, decreased expression levels, dosage compensation, stronger expression correlation, dynamic functionalization and balancing of differential expression. The potential disorders introduced by different progenitors in the allo-tetraploids were hypothesized to be alleviated by increasing structural homogeneity and performing versatile expression processes. Resequencing three common carp strains revealed two major ecotypes and uncovered candidate genes relevant to growth and survival rate.
sample list
sample id
sample name
tissue
strain
treatment
description
SRR13356954
liver
liver
nan
untreatment
liver RNA-seq replicate 1
SRR13356955
muscle
muscle
nan
untreatment
muscle RNA-seq replicate 3
SRR13356956
muscle
muscle
nan
untreatment
muscle RNA-seq replicate 2
SRR13356959
muscle
muscle
nan
untreatment
muscle RNA-seq replicate 1
SRR13356960
skin
skin
nan
untreatment
skin RNA-seq replicate 3
SRR13356961
skin
skin
nan
untreatment
skin RNA-seq replicate 2
SRR13356962
skin
skin
nan
untreatment
skin RNA-seq replicate 1
SRR13356963
spleen
spleen
nan
untreatment
spleen RNA-seq replicate 3
SRR13356964
spleen
spleen
nan
untreatment
spleen RNA-seq replicate 2
SRR13356965
spleen
spleen
nan
untreatment
spleen RNA-seq replicate 1
SRR13356966
brain
brain
nan
untreatment
brain RNA-seq replicate 3
SRR13356967
brain
brain
nan
untreatment
brain RNA-seq replicate 2
SRR13356968
brain
brain
nan
untreatment
brain RNA-seq replicate 1
SRR13356969
gill
gill
nan
untreatment
gill RNA-seq replicate 3
SRR13356970
gill
gill
nan
untreatment
gill RNA-seq replicate 2
SRR13356971
gill
gill
nan
untreatment
gill RNA-seq replicate 1
SRR13356972
heart
heart
nan
untreatment
Heart RNA-seq replicate 3
SRR13356973
heart
heart
nan
untreatment
Heart RNA-seq replicate 2
SRR13356974
heart
heart
nan
untreatment
Heart RNA-seq replicate 1
SRR13356975
intestine
intestine
nan
untreatment
intestine RNA-seq replicate 3
SRR13356977
intestine
intestine
nan
untreatment
intestine RNA-seq replicate 2
SRR13356978
intestine
intestine
nan
untreatment
intestine RNA-seq replicate 1
SRR13356979
kidney
kidney
nan
untreatment
kidney RNA-seq replicate 3
SRR13356980
kidney
kidney
nan
untreatment
kidney RNA-seq replicate 2
SRR13356981
kidney
kidney
nan
untreatment
kidney RNA-seq replicate 1
SRR13356982
liver
liver
nan
untreatment
liver RNA-seq replicate 3
SRR13356983
liver
liver
nan
untreatment
liver RNA-seq replicate 2
temperature
PRJNA478787
:
tiger barb Raw sequence reads
key word
temperature;Cold stress;Multiple tissues;Tropical stenothermal fish;Ubiquitin-mediated protein degradation;Heat shock 70 KDa protein;Cold-induced RNA-binding protein;RNA-BINDING PROTEIN;TILAPIA OREOCHROMIS-NILOTICUS;DIFFERENTIAL GENE-EXPRESSION;HSP70 MESSENGER-RNA;HEAT-SHOCK RESPONSE;GILTHEAD SEA BREAM;NILE TILAPIA;PHYSIOLOGICAL-RESPONSES;THERMAL-STRESS;COMMON CARP
publication
Liu, Lili , et al. "Transcriptome analysis reveals molecular mechanisms responsive to acute cold stress in the tropical stenothermal fish tiger barb ( Puntius tetrazona )." BMC Genomics 21.1(2020).
abstract
Background Tropical stenothermal fish exhibit special tolerance and response to cold stress. However current knowledge of the molecular mechanisms response to cold stress in aquatic ectotherms is largely drawn from eurythermal or extreme stenothermal species. The tiger barb Puntius tetrazona is a tropical stenothermal fish, with great popularity in aquarium trade and research. Results To investigate the response mechanism of P. tetrazona to low temperature, fish were exposed to increasing levels of acute cold stress. Histopathological analysis showed that the brain, gill, liver and muscle tissues appeared serious damage after cold stress (13 degrees C). Brain, gill, liver and muscle tissues from control (CTRL) groups (27 degrees C) and COLD stress groups (13 degrees C) of eight-month fish (gender-neutral) were sampled and assessed for transcriptomic profiling by high-throughput sequencing. 83.0 Gb of raw data were generated, filtered and assembled for de novo transcriptome assembly. According to the transcriptome reference, we obtained 392,878 transcripts and 238,878 unigenes, of which 89.29% of the latter were annotated. There were 23,743 differently expressed genes (DEGs) been filtered from four pairs of tissues (brain, gill, liver and muscle) between these cold stress and control groups. These DEGs were mainly involved in circadian entrainment, circadian rhythm, biosynthesis of steroid and fatty acid. There were 64 shared DEGs between the four pairs of groups, and five were related to ubiquitylation/deubiquitylation. Our results suggested that ubiquitin-mediated protein degradation might be necessary for tropical stenothermal fish coping with acute cold stress. Also, the significant cold-induced expression of heat shock 70 kDa protein (HSP70) and cold-induced RNA-binding protein (CIRBP) was verified. These results suggested that the expression of the molecular chaperones HSP70 and CIRBP in P. tetrazona might play a critical role in coping with acute cold stress. Conclusions This is the first transcriptome analysis of P. tetrazona using RNA-Seq technology. Novel findings about tropical stenothermal fish under cold stress (such as HSP70 and CIRBP genes) are presented here. This study contributes new insights into the molecular mechanisms of tropical stenothermal species response to acute cold stress.
sample list
sample id
sample name
tissue
strain
treatment
description
SRR7507732
27muscleB
muscle
nan
27C
RNA-seq of tiger barb: adult muscle-27C
SRR7507733
27liverD
liver
nan
27C
RNA-seq of tiger barb: adult liver-27C
SRR7507734
27gillA
gill
nan
27C
RNA-seq of tiger barb: adult gill-27C
SRR7507735
27brainC
brain
nan
27C
RNA-seq of tiger barb: adult brain-27C
SRR7507736
27brainB
brain
nan
27C
RNA-seq of tiger barb: adult brain-27C
SRR7507737
27brainA
brain
nan
27C
RNA-seq of tiger barb: adult brain-27C
SRR7507738
27liverB
liver
nan
27C
RNA-seq of tiger barb: adult liver-27C
SRR7507739
27liverA
liver
nan
27C
RNA-seq of tiger barb: adult liver-27C
SRR7507740
27gillC
gill
nan
27C
RNA-seq of tiger barb: adult gill-27C
SRR7507741
27gillB
gill
nan
27C
RNA-seq of tiger barb: adult gill-27C
SRR7507742
13liverC
liver
nan
13C
RNA-seq of tiger barb: adult liver-13C
SRR7507743
13muscleA
muscle
nan
13C
RNA-seq of tiger barb: adult muscle-13C
SRR7507744
13muscleB
muscle
nan
13C
RNA-seq of tiger barb: adult muscle-13C
SRR7507745
13muscleC
muscle
nan
13C
RNA-seq of tiger barb: adult muscle-13C
SRR7507746
13liverB
liver
nan
13C
RNA-seq of tiger barb: adult liver-13C
SRR7507747
13liverA
liver
nan
13C
RNA-seq of tiger barb: adult liver-13C
SRR7507748
27muscleD
muscle
nan
27C
RNA-seq of tiger barb: adult muscle-27C
SRR7507749
27muscleC
muscle
nan
27C
RNA-seq of tiger barb: adult muscle-27C
SRR7507750
13brainB
brain
nan
13C
RNA-seq of tiger barb: adult brain-13C
SRR7507751
13brainA
brain
nan
13C
RNA-seq of tiger barb: adult brain-13C
SRR7507752
13gillA
gill
nan
13C
RNA-seq of tiger barb: adult gill-13C
SRR7507753
13brainC
brain
nan
13C
RNA-seq of tiger barb: adult brain-13C
SRR7507754
13gillC
gill
nan
13C
RNA-seq of tiger barb: adult gill-13C
SRR7507755
13gillB
gill
nan
13C
RNA-seq of tiger barb: adult gill-13C
Click the
blue arrow
to add the sample you choose.
Support manual input.
IDs are separated by
space
.
note: Manually changing
the order of IDs
for drawing is supported.
Gene / RNA
Please fill in the
gene or RNA ID in FishGET
for visualization of expression.
If you have
symbol
, you can quickly search for its ID in FishGET.
Multiple symbols are supported, separated by
commas
.
More symbol need more time.
If the
co-expression
of one gene to another gene ranks more than 100, the
network
will be also visualized.
spon,fam20,cpe,slc38a3a,eed,hikeshi
Click the
blue arrow
to add the gene/RNA you choose.
Support manual input.
Support genes without symbol, and their RNA.
IDs are separated by
space
.
gene ID
RNA ID
note: Manually changing
the order of IDs
for drawing is supported.
run
reset
copyright 2021-present@Lab of Aquatic Bioinfomatics, Institute of Hydrobiology, Chinese Academy of Sciences