Search PubMed⌕ Search

PubMed · 7507216

FISH "painting" patterns resulting from complex exchanges.

Abstract

Many of the unusual patterns seen when irradiated chromosomes are FISH painted arise from Complex interchanges. In this paper, we present a method for classifying chromosome-type complex exchanges. Every possible exchange configuration for the first nine complex families has been determined, and for each of these, the expected metaphase pattern forms seen if any one of the participating chromosomes is painted, has been worked out. A total of 65 recognisably different pattern forms emerge, and a simple classification of these is provided for scoring and discussion purposes. 47 of these patterns are unique ("Tell-tale"), in that they are found in, and are diagnostic for, only one complex family or sub-family (of the sub-set analyzed). Analysis of the contingency tables indicates that: (a) The same individual complex exchange can appear in different pattern forms, depending upon which of the participating chromosomes is painted, and the converse-different forms can represent the same exchange. (b) Many different complex exchange configurations, from different families, can give rise to identical pattern forms. (c) If obvious complex forms are at all frequent in a sample, then a lot of the exchanges being scored as "simple" are not. These observations will have considerable repercussions on the numerical assessment of damage when using painted chromosomes at higher radiation doses.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

J R Savage, P J Simpson. 1994. FISH "painting" patterns resulting from complex exchanges.. https://doi.org/10.1016/0165-1161(94)90008-6

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Frequent hypermethylation of the RASSF1A gene in prostate cancer.

Recently, we have cloned and characterized the Ras association domain family 1A gene (RASSF1A) at 3p21.3, from which loss of genetic material is one of the most frequent events in several types of human solid tumors. The CpG island promoter region of this gene is highly methylated in several human cancers, most notably in small cell lung cancer, breast cancer, and renal cell carcinoma. In this study, we have analysed the methylation status of RASSF1A in primary prostate tumors and in the prostate cancer cell line LNCaP. In total, 37 out of 52 tumors (71%) were methylated at the promoter region of RASSF1A. The relative frequency of methylation was higher in more aggressive tumors compared with less malignant tumors. For instance, tumors with a Gleason score of 7-10 (25 out of 30, 83%) were significantly more methylated compared with Gleason 4-6 tumors (11 out of 20, 55%, P=0.032, Fisher's exact test). Coincident with a hypermethylated promoter, transcripts of RASSF1A were missing in LNCaP cells. Expression of RASSF1A was restored with 5-aza-2'-deoxycytidine, a DNA methylation inhibitor. In conclusion, our data suggest that epigenetic inactivation of RASSF1A by methylation is a very common event in prostate cancer and might be involved in the progression of the disease. Testing for RASSF1A methylation should become useful in prostate cancer early detection and diagnosis and might aid prognosis by gauging the potential status of progression.

Chromosome Aberrations↗

[New analytic methods provide answers regarding chromosome aberrations in 1-2 days].

During the last decade, new tools have been made available to clinical genetics laboratories through the technologies developed for gene scanning, sequencing, detection of short tandem repeats (STRs) and single nucleotide polymorphisms (SNPs). Two methods (interphase fluorescence in situ hybridization, FISH, and quantitative fluorescence PCR, QF-PCR assay) have been introduced recently for the rapid prenatal diagnosis of numerical chromosome abnormalities within 1-2 days after sample collections, thus obviating the 7-14 days delay needed for cell culture associated with conventional chromosome analysis. Most commonly, probes or STRs specific for chromosomes 13, 18, 21, X and Y are used as, depending on the indications for invasive tests, numerical abnormalities involving these chromosomes account for the vast majority of the chromosome aberrations identified prenatally. The advantage of QF-PCR over inter-phase FISH is that the former is considered substantially more cost-effective, in particular when larger sample numbers are processed.

Chromosome Aberrations↗