DNA turnover in growing yeast after X-irradiation.

نویسنده

  • H Eckstein
چکیده

Growing yeast cells incorporate radioactivity from labeled nucleotides, deoxynucleotides, deoxyadenosine, and deoxycytidine into acid-insoluble material. Most of these compounds are in­ corporated predominantly into RNA, only dTMP and dTTP serve as effective and selective DNA precursors. When yeast is prelabeled with dTMP, “specific” radioactivity of DNA decreases in the growing cells due to DNA augmentation. In X-irradiated yeast, “specific” radioactivity of DNA again de­ creases remarkably, though DNA augmentation of the growing giant cells in delayed. Simultaneous­ ly, radioactivity is rendered acid-soluble. Vice versa, X-irradiated unlabeled yeast incorporates radioactivity from labeled precursors into DNA, even if the DNA content of the cells does not increase. When growing yeast cells are treated with cycloheximide, protein synthesis and DNA augmen­ tation are inhibited completely with 5-10~"6m cycloheximide. The decrease of “specific” radio­ activity of DNA in X-irradiated cells, however, proves independent on an intact protein synthesis, even with 1 • 10—4 M cycloheximide. The data provide clear evidence on DNA turnover in growing yeast after X-irradiation.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Acid-soluble deoxynucleotides and DNA synthesis in growing yeast after x-irradiation, II. Synthesis of deoxynucleoside tri- and monophosphates in synchronized and asynchronously growing cells.

The behaviour of acid-soluble DNA precursors in synchronized and asynchronously growing yeast after X-irradiation is investigated by labeling techniques with 32P; and by enzymic estimation. In prelabeled synchronized growing cells, radioactivity associated with deoxynucleoside triphos­ phates increases to maximum values shortly before each DNA replication, followed by a drastic decrease during ...

متن کامل

YCF and YAP gene expressions in yeast cells after irradiation combined with mercury treatment

Background: All aerobically growing organisms suffer from exposure to oxidative stress, caused by partially reduced forms of molecular oxygen, known as reactive oxygen species (ROS). These are highly reactive and capable of damaging cellular constituents such as DNA, lipids and proteins. Consequently, cells from many different organisms have evolved mechanisms to protect their components...

متن کامل

Sperm DNA damage in mice irradiated with various doses of X-rays alone or in combination with actinomycin D or bleomycin sulfate: an in vivo study

Background: DNA damage in male germ cells due to exposure to environmental and manmade physico-chemical genotoxic agents is considered as the main cause of male infertility. The aim of this study was to evaluate the effects of combined modalities (radiotherapy and chemotherapy) routinely used for cancer treatment on mouse sperm chromatin in vivo. Materials and Methods: Forty-eight mice were div...

متن کامل

Nickel Increases Chromosomal Abnormalities by Interfering with the Initiation of DNA Repair Pathways

Background: Nickel is a carcinogenic, heavy metal released through industrial activities and via natural resources. It is able to cause DNA damages by reducing the efficiency of DNA repair mechanisms. However, the exact time point at which it is able to interfere with these mechanisms is not yet clearly understood. Methods: To find the most nickel-vulnerable time of repair mechanisms, human de...

متن کامل

X-irradiation of cells on glass slides has a dose doubling impact.

Immunofluorescence detection of gammaH2AX foci is a widely used tool to quantify the induction and repair of DNA double-strand breaks (DSBs) induced by ionising radiation. We observed that X-irradiation of mammalian cells exposed on glass slides induced twofold higher foci numbers compared to irradiation with gamma-rays. Here, we show that the excess gammaH2AX foci after X-irradiation are produ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Zeitschrift fur Naturforschung. Section C, Biosciences

دوره 29 1  شماره 

صفحات  -

تاریخ انتشار 1974