PUBLICATION

BCAS2 promotes primitive hematopoiesis by sequestering β-catenin within the nucleus

Authors
Ning, G., Lin, Y., Ma, H., Zhang, J., Yang, L., Liu, Z., Li, L., He, X., Wang, Q.
ID
ZDB-PUB-250614-2
Date
2025
Source
eLIFE   13: (Journal)
Registered Authors
Wang, Qiang
Keywords
BCAS2, Wnt/β-catenin, coiled-coil domain, developmental biology, mouse, nuclear retention, primitive hematopoiesis, zebrafish
Datasets
GEO:GSE297155
MeSH Terms
  • Animals
  • Wnt Signaling Pathway
  • Hematopoiesis*
  • Zebrafish/embryology
  • beta Catenin*/genetics
  • beta Catenin*/metabolism
  • Zebrafish Proteins*/genetics
  • Zebrafish Proteins*/metabolism
  • Cell Nucleus*/metabolism
  • Mice
PubMed
40511787 Full text @ Elife
Abstract
Breast carcinoma amplified sequence 2 (BCAS2), a core component of the hPrP19 complex, plays crucial roles in various physiological and pathological processes. However, whether BCAS2 has functions other than being a key RNA-splicing regulator within the nucleus remains unknown. Here, we show that BCAS2 is essential for primitive hematopoiesis in zebrafish and mouse embryos. The activation of Wnt/β-catenin signaling, which is required for hematopoietic progenitor differentiation, is significantly decreased upon depletion of bcas2 in zebrafish embryos and mouse embryonic fibroblasts. Interestingly, BCAS2 deficiency has no obvious impact on the splicing efficiency of β-catenin pre-mRNA, while significantly attenuating β-catenin nuclear accumulation. Moreover, we find that BCAS2 directly binds to β-catenin via its coiled-coil domains, thereby sequestering β-catenin within the nucleus. Thus, our results uncover a previously unknown function of BCAS2 in promoting Wnt signaling by enhancing β-catenin nuclear retention during primitive hematopoiesis.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping