Back

Role of Y box-binding protein 1 (Ybx1/ybx1) in zebrafish folliculogenesis: Promoting follicle cell proliferation via suppression of cell cycle inhibitor p21 (cdkn1a)

Zhu, B.; Zhang, Z.; Pardeshi, L.; Chen, Y.; Ge, W.

2024-03-29 developmental biology
10.1101/2024.03.27.587099 bioRxiv
Show abstract

Y box-binding protein 1 (YB-1; Ybx1/ybx1) regulates transcription and translation of targeted genes through DNA/RNA-binding. Our research in zebrafish has revealed a high abundance of Ybx1 in the primary growth (PG) follicles in the ovary, which decreases precipitously as the follicles enter the secondary growth (SG) phase. To understand the function of Ybx1 in folliculogenesis, we created an ybx1 mutant using TALEN and observed a disruption in folliculogenesis in the mutant (ybx1-/-) during the transition from previtellogenic (PV) to early vitellogenic (EV) stage of the SG phase, resulting in underdeveloped ovaries and reduced female fertility. Transcriptome and Western blot analyses identified several differentially expressed genes between mutant (ybx1-/-) and control (ybx1+/-) ovaries. Notably, the expression of cdkn1a (p21), a cell cycle inhibitor, increased dramatically in ybx1-/- follicles. Disrupting cdkn1a gene with CRISPR/Cas9 resulted in embryonic lethality. In p21 heterozygote (cdkn1a+/-), however, follicle activation and maturation in the ovary were both advanced, contrasting with the ybx1-/- mutant. Interestingly, partial loss of p21 could alleviate the phenotype of ybx1-/-. Folliculogenesis resumed in ybx1-/-;p21+/- females with normal follicle activation (PG-PV transition) and vitellogenic growth (PV-EV transition). Interestingly, the follicle cells from the ybx1-/- mutant displayed a poor proliferative activity both in vivo and in vitro; however, the cells from the ybx1-/-;p21+/- follicles resumed normal proliferation. In conclusion, our study suggests that Ybx1 serves a pivotal role in controlling early folliculogenesis in zebrafish, and its acts, at least partly, by repressing the expression of cdkn1a, a cell cycle inhibitor.

Matching journals

The top 6 journals account for 50% of the predicted probability mass.

1
Frontiers in Cell and Developmental Biology
233 papers in training set
Top 0.1%
18.3%
2
Developmental Biology
150 papers in training set
Top 0.2%
10.9%
3
eLife
5828 papers in training set
Top 19%
6.2%
4
Development
497 papers in training set
Top 1%
5.5%
5
Developmental Dynamics
56 papers in training set
Top 0.1%
5.4%
6
PLOS ONE
5266 papers in training set
Top 29%
5.4%
50% of probability mass above
7
Biology of Reproduction
36 papers in training set
Top 0.2%
5.1%
8
Scientific Reports
3612 papers in training set
Top 23%
4.3%
9
PLOS Genetics
862 papers in training set
Top 3%
4.0%
10
Endocrinology
43 papers in training set
Top 0.2%
4.0%
11
iScience
1154 papers in training set
Top 11%
2.4%
12
The FASEB Journal
194 papers in training set
Top 2%
2.1%
13
Proceedings of the National Academy of Sciences
2444 papers in training set
Top 26%
1.9%
14
Genes to Cells
25 papers in training set
Top 0.2%
1.9%
15
Aquaculture
31 papers in training set
Top 0.3%
1.4%
16
Journal of Experimental Zoology Part B: Molecular and Developmental Evolution
22 papers in training set
Top 0.3%
1.3%
17
Journal of Genetics and Genomics
38 papers in training set
Top 0.7%
0.8%
18
G3 Genes|Genomes|Genetics
351 papers in training set
Top 4%
0.8%
19
Frontiers in Physiology
106 papers in training set
Top 3%
0.8%
20
International Journal of Molecular Sciences
494 papers in training set
Top 15%
0.8%
21
PNAS Nexus
159 papers in training set
Top 3%
0.8%
22
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
26 papers in training set
Top 1%
0.6%
23
Journal of Neuroendocrinology
22 papers in training set
Top 0.4%
0.6%
24
Open Biology
106 papers in training set
Top 2%
0.6%
25
Frontiers in Endocrinology
58 papers in training set
Top 2%
0.6%
26
Journal of Heredity
42 papers in training set
Top 1%
0.6%