<i>Jumping Translocation Breakpoint</i> Expression in Midgestation Mouse Embryos.
Ontology highlight
ABSTRACT: Jumping translocations (JTs) can lead to partial trisomies. A breakpoint within the gene known as Jumping Translocation Breakpoint (JTB) has previously been associated with JTs involving the long arm of human chromosome 1 (1q). These 1q+ amplifications are frequently observed in cancer. JTB was initially mapped to the Epidermal Differentiation Complex (EDC) at 1q21, and earlier studies primarily focused on its role in malignant or adult tissues. Using updated genomic data, we refined the mapping of JTB. We employed RNA in situ hybridization (RISH) to visualize Jtb expression with organ, tissue, and cell-level resolution. We demonstrate that human JTB and murine Jtb are located outside the EDC. In midgestational wild-type mouse embryos, Jt
SUBMITTER: McGrath C
PROVIDER: S-EPMC12562924 | biostudies-literature | 2025 Oct
REPOSITORIES: biostudies-literature
ACCESS DATA