Regulation of Protein Synthesis during Density-dependent Growth Inhibition of BHK21/13 Cells
Regulation of protein synthesis in BHK21/13 cells has been examined as a function of cell growth rate and density, both in vivo by pulse-labeling of cells with [ 3 H]valine and in an in vitro cell-free protein-synthesizing system. The specific activity of [ 3 H]valyl-tRNA in the pulse-labeled cells...
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Veröffentlicht in: | The Journal of biological chemistry 1974-06, Vol.249 (11), p.3483-3488 |
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container_title | The Journal of biological chemistry |
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creator | Baenziger, N L Jacobi, C H Thach, R E |
description | Regulation of protein synthesis in BHK21/13 cells has been examined as a function of cell growth rate and density, both in vivo by pulse-labeling of cells with [ 3 H]valine and in an in vitro cell-free protein-synthesizing system. The specific activity of [ 3 H]valyl-tRNA in the pulse-labeled cells was determined and the true in vivo rate of [ 3 H]valine incorporation into protein was measured. Unlike the reported behavior of many other cell lines, BHK21/13 cells did
not shut off their protein synthesis at all while their growth rate declined 10-fold or more during density-dependent inhibition
of growth or during arrest of growth by serum deprivation. In vitro assays of the cells' protein synthetic activity with both synthetic and natural messenger RNA confirmed that all of the components
needed for protein synthesis were equally active in rapidly growing and in density-inhibited or serum-deprived cells. Hence,
in these cells the protein synthesis rate and the cell division rate are not coupled, and the amount of protein in the cell
is not regulated at the level of synthesis, but rather at the level of protein degradation or export. |
doi_str_mv | 10.1016/S0021-9258(19)42598-2 |
format | Article |
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not shut off their protein synthesis at all while their growth rate declined 10-fold or more during density-dependent inhibition
of growth or during arrest of growth by serum deprivation. In vitro assays of the cells' protein synthetic activity with both synthetic and natural messenger RNA confirmed that all of the components
needed for protein synthesis were equally active in rapidly growing and in density-inhibited or serum-deprived cells. Hence,
in these cells the protein synthesis rate and the cell division rate are not coupled, and the amount of protein in the cell
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not shut off their protein synthesis at all while their growth rate declined 10-fold or more during density-dependent inhibition
of growth or during arrest of growth by serum deprivation. In vitro assays of the cells' protein synthetic activity with both synthetic and natural messenger RNA confirmed that all of the components
needed for protein synthesis were equally active in rapidly growing and in density-inhibited or serum-deprived cells. Hence,
in these cells the protein synthesis rate and the cell division rate are not coupled, and the amount of protein in the cell
is not regulated at the level of synthesis, but rather at the level of protein degradation or export.</description><subject>Alanine - metabolism</subject><subject>Animals</subject><subject>Autoradiography</subject><subject>Carbon Radioisotopes</subject><subject>Cell Division</subject><subject>Cell Line</subject><subject>Cell-Free System</subject><subject>Cricetinae</subject><subject>Culture Media</subject><subject>Encephalomyocarditis virus</subject><subject>Fibroblasts - metabolism</subject><subject>Globins</subject><subject>Kidney - growth & development</subject><subject>Kidney - metabolism</subject><subject>Kinetics</subject><subject>Poly U - pharmacology</subject><subject>Protein Biosynthesis</subject><subject>Proteins - metabolism</subject><subject>RNA, Messenger - metabolism</subject><subject>RNA, Transfer - metabolism</subject><subject>RNA, Viral</subject><subject>Transfer RNA Aminoacylation</subject><subject>Tritium</subject><subject>Valine - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1974</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kFtLw0AQhRdRaq3-hEJAEH2I3dnNJtlHrdqKBcUq-CAsuUyalXZTdxNK_73pxc7LPJxzZg4fIX2gt0AhHEwpZeBLJuJrkDcBEzL22RHpAo25zwV8HZPuwXJKzpz7oe0EEjqkE_AwCEXUJd_vOGvmSa0r41WF92arGrXxpmtTl-i08_LGajPzHtA4Xa_9HJdocjS1N7LVqi69Z1PqVP_n78cvDAbAvSHO5-6cnBTJ3OHFfvfI59Pjx3DsT15Hz8O7iZ_xSNZ-kksWByGVDGUW5iyLUxBRhIlAARFjWSqjkENchEzkiDIVmIuIySKMBEsSznvkand3aavfBl2tFtplbYPEYNU4FbOAci5laxQ7Y2Yr5ywWamn1IrFrBVRtqKotVbVBpkCqLVXF2lx__6BJF5gfUnuMrX6500s9K1faokp1lZW4UCyQCkDxIOb8D3Y9fac</recordid><startdate>19740610</startdate><enddate>19740610</enddate><creator>Baenziger, N L</creator><creator>Jacobi, C H</creator><creator>Thach, R E</creator><general>American Society for Biochemistry and Molecular Biology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19740610</creationdate><title>Regulation of Protein Synthesis during Density-dependent Growth Inhibition of BHK21/13 Cells</title><author>Baenziger, N L ; Jacobi, C H ; Thach, R E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-ad92846092e9c6d2c8b1577ea5e51722cb976318f625dee9b5ed5729f6752aa33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1974</creationdate><topic>Alanine - metabolism</topic><topic>Animals</topic><topic>Autoradiography</topic><topic>Carbon Radioisotopes</topic><topic>Cell Division</topic><topic>Cell Line</topic><topic>Cell-Free System</topic><topic>Cricetinae</topic><topic>Culture Media</topic><topic>Encephalomyocarditis virus</topic><topic>Fibroblasts - metabolism</topic><topic>Globins</topic><topic>Kidney - growth & development</topic><topic>Kidney - metabolism</topic><topic>Kinetics</topic><topic>Poly U - pharmacology</topic><topic>Protein Biosynthesis</topic><topic>Proteins - metabolism</topic><topic>RNA, Messenger - metabolism</topic><topic>RNA, Transfer - metabolism</topic><topic>RNA, Viral</topic><topic>Transfer RNA Aminoacylation</topic><topic>Tritium</topic><topic>Valine - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baenziger, N L</creatorcontrib><creatorcontrib>Jacobi, C H</creatorcontrib><creatorcontrib>Thach, R E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baenziger, N L</au><au>Jacobi, C H</au><au>Thach, R E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of Protein Synthesis during Density-dependent Growth Inhibition of BHK21/13 Cells</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1974-06-10</date><risdate>1974</risdate><volume>249</volume><issue>11</issue><spage>3483</spage><epage>3488</epage><pages>3483-3488</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Regulation of protein synthesis in BHK21/13 cells has been examined as a function of cell growth rate and density, both in vivo by pulse-labeling of cells with [ 3 H]valine and in an in vitro cell-free protein-synthesizing system. The specific activity of [ 3 H]valyl-tRNA in the pulse-labeled cells was determined and the true in vivo rate of [ 3 H]valine incorporation into protein was measured. Unlike the reported behavior of many other cell lines, BHK21/13 cells did
not shut off their protein synthesis at all while their growth rate declined 10-fold or more during density-dependent inhibition
of growth or during arrest of growth by serum deprivation. In vitro assays of the cells' protein synthetic activity with both synthetic and natural messenger RNA confirmed that all of the components
needed for protein synthesis were equally active in rapidly growing and in density-inhibited or serum-deprived cells. Hence,
in these cells the protein synthesis rate and the cell division rate are not coupled, and the amount of protein in the cell
is not regulated at the level of synthesis, but rather at the level of protein degradation or export.</abstract><cop>United States</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>4364657</pmid><doi>10.1016/S0021-9258(19)42598-2</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Alanine - metabolism Animals Autoradiography Carbon Radioisotopes Cell Division Cell Line Cell-Free System Cricetinae Culture Media Encephalomyocarditis virus Fibroblasts - metabolism Globins Kidney - growth & development Kidney - metabolism Kinetics Poly U - pharmacology Protein Biosynthesis Proteins - metabolism RNA, Messenger - metabolism RNA, Transfer - metabolism RNA, Viral Transfer RNA Aminoacylation Tritium Valine - metabolism |
title | Regulation of Protein Synthesis during Density-dependent Growth Inhibition of BHK21/13 Cells |
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