Viral oncogenes and cellular prototypes.
نویسندگان
چکیده
The structural hallmark of retroviral transforming onc genes is a specific RNA sequence that is unrelated to the essential retroviral genes but closely related to certain cellular prototypes termed proto-onc genes. Two types of onc genes have been distinguished. Type I are onc genes which utilize elements of specific sequences only to encode a transforming protein. Type I1 onc genes are hybrids which utilize essential viral (typically gag) and specific RNA sequences to encode transforming proteins. Comparisons between viral onc genes and cellular proto-onc genes are reviewed in the light of two competing models for protoonc function: the quantitative model, which holds that viral onc genes and cellular proto-onc genes are functionally the Same and that transformation is the result of enhanced dosage of a cellular proto-onc gene; and the qualitative model, which holds that they are different. Structural comparisons between viral onc genes and cellular prototypes have demonstrated extensive sequence homologies in the primary structures of the specific sequences. However, qualitative differences exist in the structure and organization of viral onc genes and cellular prototypes. These include differences in promoters, minor differences in the primary structure of shared sequences, and absolute differences such as in the
منابع مشابه
The Effect of Herpes Simplex Virus Virion Host Shutoff Gene- a New Suicide Gene- on Tumor Cells
Background: The herpes simplex virus (HSV) UL41 gene product, virion host shutoff (Vhs) protein, mediates the rapid degradation of both viral and cellular mRNA. This ability suggests that Vhs protein can be used as a suicide gene in cancer gene therapy applications. The recent reports have shown that the degradation of cellular mRNA during herpes simplex infection is selective. RNA containing A...
متن کاملMonoclonal antibodies against the viral and human cellular myb gene product.
Retroviruses code for oncogenes which cause tumors in animals. The viral oncogenes have evolved from normal cellular proto-oncogenes, to which they are closely related. The viral and cellular oncogenes differ in point mutations and size, the viral genes often being truncated and, in some cases, fused to unrelated cellular genes. These differences may be responsible for the transforming function...
متن کاملOncogenes of DNA Tumor Viruses1
Experiments carried out over the past 10-12 years have created a field or approach which may properly be termed the molecular basis of cancer. One of its major accomplishments has been the identification and understanding of some of the functions of a group of cancer-causing genes, the oncogenes. The major path to the oncogenes came from the study of cancercausing viruses. The oncogenes have be...
متن کاملRoles of growth factor activities in oncogenesis.
I NSIGHT into normal and abnormal cell growth and differentiation may be obtained by identifying and analyzing the activity of highly specific genes, called oncogenes, whose coding sequences contain the information necessary to initiate and maintain neoplastic transformation. The identification of oncogenes and the characterization of the structure and function of these genes have progressed ra...
متن کاملMultiple-Integrations of HPV16 Genome and Altered Transcription of Viral Oncogenes and Cellular Genes Are Associated with the Development of Cervical Cancer
The constitutive expression of the high-risk HPV E6 and E7 viral oncogenes is the major cause of cervical cancer. To comprehensively explore the composition of HPV16 early transcripts and their genomic annotation, cervical squamous epithelial tissues from 40 HPV16-infected patients were collected for analysis of papillomavirus oncogene transcripts (APOT). We observed different transcription pat...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Haematology and blood transfusion
دوره 28 شماره
صفحات -
تاریخ انتشار 1983