Introduction

Abstract

RNA tumor viruses¹ have become increasingly utilized in studies of cellular transformation and gene regulation. The genes of retroviruses exist in two forms; as extrachromosomal, RNA-eontaining, infectious particles and as DNA pro-viruses² stably associated with cell genes. Components from the extracellular form can be collected in large quantity and purified for the preparation of molecular probes. These probes can be used to dissect the sequence of events required for the establishment and expression of the integrated form. Furthermore the genomes of retroviruses originated from normal cell genes, genes called virogenes². The nucleic acid and protein probes isolated from these viruses are therefore useful for studying the nature and expression of this normal cell gene and in elucidating the physiological role of its products. RNA tumor viruses perhaps offer us one of the most complete sets of biochemical reagents and biological responses for examining gene regulation in vertebrates and for studying the consequences of aberrant gene regulation on cell growth in tissue culture and in animals. Furthermore, there is an increasing conviction that virogenes play an important role in normal development and/or differentiation (Risser, Stockert and Old, 1978). Consequently, there is a growing feeling that DNA proviruses are altered virogenes and are capable of interfering with normal development or differentiation, causing reprogrammed growth or the incapacity to specialize.