Cell fusion-induced quick change in replication time of the inactive mouse X chromosome: an implication for the maintenance mechanism of late replication

EMBO J. 1993 Nov;12(11):4397-405. doi: 10.1002/j.1460-2075.1993.tb06124.x.

Abstract

It is unknown how and why the genetically inactivated mammalian X chromosome replicates late in S phase. There are also occasional inactive X chromosomes characterized by an opposite behavior replicating early in S phase. Two clonal cell lines, MTLB3 and MTLH8, isolated from a cultured murine T-cell lymphoma have an allocyclic X chromosome of the latter type. This precociously replicating X chromosome was judged to be genetically inactive as the late replicating one. Immediately after fusion with another cell line, the precociously replicating X chromosome from these cells starts to replicate late in S phase. This finding seems to suggest that late replication characterizing the inactive X chromosome is actively maintained by a trans-acting factor in female somatic cells, and that its lack entails a switch from late replication to precocious replication. It remains unknown whether this presumptive factor also modifies the autosomal replication pattern.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cell Cycle / genetics*
  • DNA Replication*
  • Dosage Compensation, Genetic*
  • Female
  • Gene Expression Regulation*
  • Hybrid Cells
  • Karyotyping
  • Male
  • Mice
  • Molecular Sequence Data
  • S Phase / genetics
  • Tumor Cells, Cultured