Construction and Analysis of Painting Probe for Homogeneously Staining Regions in Human Neuroblastoma Cell line IMR-32.
- Author:
Sun Hwa PARK
1
;
Ho Chung KIM
;
Yong Hyuck CHUN
Author Information
1. Department of Anatomy, College of Medicine, Korea University, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
2p24;
2p13;
HSRs;
IMR-32;
Microdissection;
Painting probe
- MeSH:
Cell Line*;
Chromosomes, Human, Pair 2;
DNA;
DNA Topoisomerases, Type I;
DNA, Superhelical;
Genes, myc;
Humans*;
In Situ Hybridization, Fluorescence;
Microdissection;
Needles;
Neural Crest;
Neuroblastoma*;
Paint*;
Paintings*;
Polymerase Chain Reaction;
Relaxation;
Virulence
- From:Journal of Genetic Medicine
1997;1(1):45-50
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Painting probe for HSRs in IMR-32 Neuroblastoma, a pediatric malignant neoplasm of neural crest origin, has a wide range of clinical virulence. The mechanisms contributing to the development of neuroblastomas are largely unclear, but non-random chromosomal changes identified over the past years suggest the involvement of genetic alterations. Amplification of the human N-myc proto-oncogene is frequently seen either in extrachromosomal double minutes or in homogeneously staining regions(HSRs) of aggressively growing neuroblastomas. N-myc maps to chromosome 2 band 24, but HSR have never been observed at this band, suggesting transposition of N-myc during amplification. We have constructed and analyzed the region-specific painting probe for HSR in neuroblastoma IMR-32 to determine the derivative chromosomes. Microdissection was performed on HSR using an inverted microscope with the help of microglass needles and an micromanipulator. We pretreated the microdissected fragments with Topoisomerase I which catalyzes the relaxation of supercoiled DNA, and performed two initial rounds of DNA synthesis with T7 DNA polymerase followed by conventional PCR to enable the reliable preparation of Fluorescent in situ hybridization probe from a single microdissected chromosome. With this method, it was possible to construct the region-specific painting probe for HSR. The probe hybridized specifically to the HSRs of IMR-32, and to 2p24, 2p13 of normal chromosome. Our results suggest there was coamplification of N-myc together with DNA of the chromosome 2p24 and 2p13. Moreover, the fluorescent signals for the amplified chromosomal regions in IMR-32 cells were also easily recognized at a Thus this painting probe can be applied to detect the similar amplification of N-myc in neuroblastoma tissue, and the probe pool for HSR may be used to identify the cancer-relevant genes.
