Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death.

Hicks GG, Singh N, Nashabi A, Mai S, Bozek G, Klewes L, Arapovic D, White EK, Koury MJ, Oltz EM, Van Kaer L, Ruley HE
Nat Genet. 2000 24 (2): 175-9

PMID: 10655065 · DOI:10.1038/72842

The gene FUS (also known as TLS (for translocated in liposarcoma) and hnRNP P2) is translocated with the gene encoding the transcription factor ERG-1 in human myeloid leukaemias. Although the functions of wild-type FUS are unknown, the protein contains an RNA-recognition motif and is a component of nuclear riboprotein complexes. FUS resembles a transcription factor in that it binds DNA, contributes a transcriptional activation domain to the FUS-ERG oncoprotein and interacts with several transcription factors in vitro. To better understand FUS function in vivo, we examined the consequences of disrupting Fus in mice. Our results indicate that Fus is essential for viability of neonatal animals, influences lymphocyte development in a non-cell-intrinsic manner, has an intrinsic role in the proliferative responses of B cells to specific mitogenic stimuli and is required for the maintenance of genomic stability. The involvement of a nuclear riboprotein in these processes in vivo indicates that Fus is important in genome maintenance.

MeSH Terms (21)

Animals Animals, Newborn B-Lymphocytes Bone Marrow Cells Chimera Crosses, Genetic Female Genotype Heterogeneous-Nuclear Ribonucleoproteins Humans Liver Lymphocyte Activation Male Mice Mice, Inbred C57BL Mice, Knockout Restriction Mapping Ribonucleoproteins RNA-Binding Protein FUS RNA-Binding Proteins Spleen

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