학술논문

Essential developmental, genomic stability, and tumour suppressor functions of the mouse orthologue of hSSB1/NABP2.
Document Type
article
Source
PLoS genetics. 9(2)
Subject
B-Lymphocytes
Fibroblasts
Animals
Humans
Mice
Infertility
Male
Chromosome Breakage
Genomic Instability
Carrier Proteins
Nuclear Proteins
Histones
Transcription Factors
Signal Transduction
Spermatogenesis
DNA Repair
Gene Expression Regulation
Developmental
Radiation
Ionizing
Radiation Tolerance
Male
Suppressor of Cytokine Signaling Proteins
DNA Breaks
Double-Stranded
Homologous Recombination
Developmental Biology
Genetics
Language
Abstract
Single-stranded DNA binding proteins (SSBs) regulate multiple DNA transactions, including replication, transcription, and repair. We recently identified SSB1 as a novel protein critical for the initiation of ATM signaling and DNA double-strand break repair by homologous recombination. Here we report that germline Ssb1(-/-) embryos die at birth from respiratory failure due to severe rib cage malformation and impaired alveolar development, coupled with additional skeletal defects. Unexpectedly, Ssb1(-/-) fibroblasts did not exhibit defects in Atm signaling or γ-H2ax focus kinetics in response to ionizing radiation (IR), and B-cell specific deletion of Ssb1 did not affect class-switch recombination in vitro. However, conditional deletion of Ssb1 in adult mice led to increased cancer susceptibility with broad tumour spectrum, impaired male fertility with testicular degeneration, and increased radiosensitivity and IR-induced chromosome breaks in vivo. Collectively, these results demonstrate essential roles of Ssb1 in embryogenesis, spermatogenesis, and genome stability in vivo.