1764 Chromosomes and Oncogenes In
نویسندگان
چکیده
The cells from plasmacytomas induced in BALB/c and susceptible BALB/c congenic strains of mice by pristane (2,6,10,14-tetramethylpentadecane) (1) have non-random chromosomal translocations, rcpt (6;15) or rcpt(12;15) (2, 3). To date, the karyotypes of 27 early transfer generation or primary pristine-induced plasmacytomas have determined, and 26 of the tumors have either rcpt(6; 15) or rcpt(12;15) (3-5). The transiocation breakpoints on these chromosomes occur in the same chromosome bands in all the plasmacytomas studied to date. The breakpoints in chromosomes 12 and 15 have been studied by cloning and DNA sequencing. The breakpoint in chromosome 12 occurs in the immunoglobulin heavy chain gene (IgH) ~ complex, frequently, but not always, in the switch region of the alpha heavy chain gene (6-11). In chromosome 15 the breakpoint occurs close to or within the c-myc oncogene (8-12). The breakpoints in chromosome 6 have not yet been determined. Expression of c-myc RNA, often in relatively large amounts, characterized most of the plasmacytomas (11, 13, 14), and rearrangement of c-myc DNA was frequently seen. The development of plasma cell tumors in BALB/c mice injected with pristane alone requires a minimum of 120 d, but usually more than 200 d (15). In contrast, plasmacytomagenesis can be greatly accelerated (5, 16) by infecting pristane-injected mice with Abelson virus. This murine acute leukemia virus contains two retroviral elements, a replication competent Moloney leukemia virus helper and a defective component, A-MuLV (17). The defective element has lost part or all of the viral gag, pol, and env genes and has acquired sequences from the mouse c-abl gene (for review see reference 18). Adult mice of only a This work was supported in part by a Grant-in-Aid for Cancer Research from the Ministry of Education, Science and Culture, Japan, and by grants from the National Cancer Institute, Dept. of Health and Human Services, and The Swedish Cancer Society. 1 Abbreviations used in this paper: ABPC, plasmacytomas induced by Abelson virus plus pristane; A-MuLV, Abelson murine leukemia virus; IgH, immunoglobulin heavy chain; i.p., intraperitoneal; LTR, long terminal repeats of retroviruses; rcpt, reciprocal chromosome transiocation.
منابع مشابه
Identification of Human Chromosome Segments that Have High Homology with Rat Genomic DNA
This study was conducted to determine the location of DNA segment with homology to the rat conserved genomic DNA in human chromosomes. The labeled rat genomic DNA was hybridized with normal human (male) metaphases. The study of 74 metaphases after fluorescence in situ hybridization showed 371 twin-spot signals on human chromosomes. Statistical analysis indicated that the specific accumulation o...
متن کاملMutations at Nucleotide 1762, 1764 and 1766 of Hepatitis B Virus X Gene in Patients with Chronic Hepatitis B and Hepatitis B-Related Cirrhosis
Abstract Background and objective: Hepatitis B virus (HBV) is a DNA virus with high tendency toward hepatic tissue. There are currently about 3 million HBV-infected people and 350 to 400 million chronic carriers of this virus in the world. X protein plays a role in the over-expression of oncogenes, carcinogenicity of liver cells and overlaps with the basal co...
متن کاملRelevanz von Aberrationen des Chromosoms 13 bei kaninen Tumoren
For human tumours there are many reports documenting the correlation between chromosome aberrations and tumour entities. Due to the complex canine karyotypic pattern (78 chromosomes), cytogenetic studies of tumours of the dog are rare. However, the reports in the literature show, that canine chromosome 13 (CFA 13) is predominantly involved in chromosomal changes. Interestingly, CFA 13 shows hig...
متن کاملOncogenes and antioncogenes in lung tumorigenesis.
The role of oncogenes and antioncogenes in lung tumorigenesis is discussed in this review, with particular emphasis on their prognostic significance. Mutations in the ras family of oncogenes, overexpression of the myc and neu families of oncogenes, and mutations of p53, the recessive tumor suppressor gene, occur with differing frequencies in small cell lung cancer and non-small cell lung cancer...
متن کاملIdentification of a Recurring Translocation Site Involving Chromosome 6 in Human Malignant Melanoma1
The recognition of recurring sites of chromosome change in human cancers has pinpointed the location in the genome of several important growth-regulatory sequences (e.g., cellular oncogenes). This report details the finding of a recurring translocation site involving the long arm of chromosome 6 (6q) in malignant melanoma. We have observed a translocation (I) between chromosomes I and 6 in five...
متن کامل