Hi-C detects novel structural variants in HL-60 and HL-60/S4 cell lines

Genomics. 2020 Jan;112(1):151-162. doi: 10.1016/j.ygeno.2019.05.009. Epub 2019 May 13.

Abstract

Cancer cell lines often have large structural variants (SVs) that evolve over time. There are many reported differences in large scale SVs between HL-60 and HL-60/S4, two cell lines derived from the same acute myeloid leukemia sample. However, the stability and variability of inter- and intra-chromosomal structural variants between different sources of the same cell line is unknown. Here, we used Hi-C and RNA-seq to identify and compare large SVs in HL-60 and HL-60/S4 cell lines. Comparisons with previously published karyotypes identified novel SVs in both cell lines. Hi-C was used to characterize the known expansion centered on the MYC locus. The MYC expansion was integrated into known locations in HL-60/S4, and a novel location (chr4) in HL-60. The HL-60 cell line has more within-line structural variation than the HL-60/S4 derivative cell line. Collectively we demonstrate the usefulness of Hi-C and with RNA-seq data for the identification and characterization of SVs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatin
  • Chromosomes, Human*
  • Gene Fusion
  • Genetic Variation*
  • Genome, Human
  • HL-60 Cells
  • Humans
  • Karyotype
  • Protein Biosynthesis
  • Proto-Oncogene Proteins c-myc / genetics
  • RNA-Seq

Substances

  • Chromatin
  • MYC protein, human
  • Proto-Oncogene Proteins c-myc