Zebrafish usp39 mutation leads to rb1 mRNA splicing defect and pituitary lineage expansion.
Loss of retinoblastoma (Rb) tumor suppressor function is associated with human malignancies. Molecular and genetic mechanisms responsible for tumorigenic Rb downregulation are not fully defined. Through a forward genetic screen and positional cloning, we identified and characterized a zebrafish ubiq...
Main Authors: | Yesenia Ríos, Shlomo Melmed, Shuo Lin, Ning-Ai Liu |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2011-01-01
|
Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC3020934?pdf=render |
Similar Items
-
Lineage-specific restraint of pituitary gonadotroph cell adenoma growth.
by: Vera Chesnokova, et al.
Published: (2011-03-01) -
The Deubiquitinase USP39 Promotes ESCC Tumorigenesis Through Pre-mRNA Splicing of the mTORC2 Component Rictor
by: Yuan Zhao, et al.
Published: (2021-05-01) -
Splicing factor USP39 promotes ovarian cancer malignancy through maintaining efficient splicing of oncogenic HMGA2
by: Shourong Wang, et al.
Published: (2021-03-01) -
Rb regulates fate choice and lineage commitment in vivo
by: Calo, Eliezer, et al.
Published: (2012) -
pRb's role in cell fate, lineage commitment, and tumorigenesis
by: Calo-Velázquez, Eliezer
Published: (2011)