Transcriptomic profile of early zebrafish PGCs by single cell sequencing.
Xiaoyuan Zhang1,2,3, Xintian Li1,2,3, Ronghong Li1,2,3
1State Key Laboratory of Cell Biology, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai, China.
Plos One
|August 15, 2019
Summary
This study used single cell RNA-sequencing to analyze zebrafish primordial germ cells (PGCs) across three developmental stages. Gene expression changes reveal PGCs primarily migrate and divide early, then focus on translation later in development.
Area of Science:
- Developmental Biology
- Genomics
- Zebrafish Research
Background:
- Primordial germ cells (PGCs) are crucial for reproduction.
- Understanding PGC development provides insights into early embryogenesis.
- Zebrafish serve as a valuable model organism for studying developmental processes.
Purpose of the Study:
- To investigate the transcriptomic profile of early zebrafish PGCs at single-cell resolution.
- To identify gene expression patterns associated with PGC development.
- To elucidate the functional roles of genes during PGC formation and migration.
Main Methods:
- Single cell RNA-sequencing (scRNA-seq) was performed on zebrafish PGCs at 6, 11, and 24 hours post fertilization (hpf).
- Weighted gene co-expression network analysis (WGCNA) was employed to identify gene modules.
- Functional enrichment analysis and differential gene expression analysis were conducted.
Main Results:
- Gene detection varied across developmental stages, with fewer genes expressed as development progressed.
- scRNA-seq data clustered samples by developmental stage, indicating distinct transcriptomic profiles.
- WGCNA identified key gene modules related to PGC formation, migration, and translation.
Conclusions:
- Zebrafish PGCs exhibit distinct functional shifts from migration/division to translation during early development.
- Gene expression patterns suggest a significant decrease in PGC formation/migration genes between 11 and 24 hpf.
- This study provides foundational single-cell data for zebrafish PGC development.
Related Concept Videos
Cis-regulatory Sequences
11.6K
Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
11.6K
Cis-regulatory Sequences
4.0K
4.0K
Ribosome Profiling
4.1K
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
4.1K
Sanger Sequencing
773.4K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
773.4K
Next-generation Sequencing
97.9K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
97.9K
Maxam-Gilbert Sequencing
12.7K
In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
Challenges of the Maxam-Gilbert Method
The...
12.7K


