Specific DNA sequence amplification in human neuroblastoma cells.

KT Montgomery(Cornell University), June L. Biedler(Cornell University), Barbara A. Spengler(Cornell University), Peter W. Melera(Cornell University)
Proceedings of the National Academy of Sciences
September 1, 1983
Cited by 71Open Access
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Abstract

Southern blot analysis of a number of EcoRI-digested human neuroblastoma DNAs has revealed the presence of a family of discrete restriction fragments, the majority of which are amplified in most, but not all, of the neuroblastoma cell lines tested. None of these sequences is abundantly present in DNA from other human tumors of different tissue origins, including several either known or presumed to contain amplified DNA. Hence, these sequences appear to be specifically amplified by neuroblastoma cells. Hybridization with metaphase chromosomes in situ has localized these sequences to either the homogeneously staining regions or double-minute chromosomes of different neuroblastoma cell lines, indicating that these chromosomal structures, although present in cell lines established from different patients, share many sequences and may have a common, but as yet unknown, function.


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