Purified vesicular stomatitis virus was disrupted with Triton N101 and treated with micrococcal nuclease. The genome RNA (42S) within the ribonucleoprotein (RNP) core contained nuclease-sensitive sites. At least 60% of the genome RNA sedimented around the 31S region following nuclease treatment; the rest was totally resistant. Transcriptase activities and synthesis of viral mRNA by the nuclease-treated or untreated virions were identical. Sites of the nuclease action appeared around the center of the genome RNA. The 3''-terminal promotor region of the genome RNA within the RNP core was inaccessible to the nuclease action after removal of the L and the NS proteins from it. The structure and function of the RNP core are discussed.