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Differential Response of Mouse Male Germ-Cell Stages to Radiation-Induced Specific-Locus and Dominant Mutations
In an attempt to provide a systematic assessment of the frequency and nature of mutations induced in successive stages of spermato- and spermiogenesis, X-irradiated male mice were re-mated at weekly intervals, and large samples of progeny, observed from birth onward, were scored and genetically test...
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Published in: | Genetics (Austin) 1998-04, Vol.148 (4), p.1567-1578 |
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description | In an attempt to provide a systematic assessment of the frequency and nature of mutations induced in successive stages of spermato- and spermiogenesis, X-irradiated male mice were re-mated at weekly intervals, and large samples of progeny, observed from birth onward, were scored and genetically tested for recessive mutations at seven specific loci and for externally recognizable dominant mutations. Productivity findings provided a rough measure of induced dominant-lethal frequencies. A qualitative assessment of specific-locus mutations (which include deletions and other rearrangements) was made on the basis of homozygosity test results, as well as from information derived from more recent complementation studies and molecular analyses. Both recessive and dominant visibles revealed clear distinctions between spermatogonia and postspermatogonial stages. In addition, differences for both of these endpoints, as well as for presumed dominant lethals, were found among various postspermatogonial stages. It may be concluded that radiation produces its maximum rates of genetic damage in germ-cell stages ranging from midpachytene spermatocytes through early spermatids, a pattern unlike any of those that have been defined for chemicals; further, the frequency peaks for radiation are lower and broader. The difference between post-stem-cell stages overall and stem-cell spermatogonia was smaller than is generally found with chemicals, not only with respect to the frequency but also the nature of mutations. |
doi_str_mv | 10.1093/genetics/148.4.1567 |
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Both recessive and dominant visibles revealed clear distinctions between spermatogonia and postspermatogonial stages. In addition, differences for both of these endpoints, as well as for presumed dominant lethals, were found among various postspermatogonial stages. It may be concluded that radiation produces its maximum rates of genetic damage in germ-cell stages ranging from midpachytene spermatocytes through early spermatids, a pattern unlike any of those that have been defined for chemicals; further, the frequency peaks for radiation are lower and broader. 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L</creatorcontrib><creatorcontrib>Bangham, Jean W</creatorcontrib><creatorcontrib>Russell, Liane B</creatorcontrib><title>Differential Response of Mouse Male Germ-Cell Stages to Radiation-Induced Specific-Locus and Dominant Mutations</title><title>Genetics (Austin)</title><addtitle>Genetics</addtitle><description>In an attempt to provide a systematic assessment of the frequency and nature of mutations induced in successive stages of spermato- and spermiogenesis, X-irradiated male mice were re-mated at weekly intervals, and large samples of progeny, observed from birth onward, were scored and genetically tested for recessive mutations at seven specific loci and for externally recognizable dominant mutations. Productivity findings provided a rough measure of induced dominant-lethal frequencies. A qualitative assessment of specific-locus mutations (which include deletions and other rearrangements) was made on the basis of homozygosity test results, as well as from information derived from more recent complementation studies and molecular analyses. Both recessive and dominant visibles revealed clear distinctions between spermatogonia and postspermatogonial stages. In addition, differences for both of these endpoints, as well as for presumed dominant lethals, were found among various postspermatogonial stages. It may be concluded that radiation produces its maximum rates of genetic damage in germ-cell stages ranging from midpachytene spermatocytes through early spermatids, a pattern unlike any of those that have been defined for chemicals; further, the frequency peaks for radiation are lower and broader. The difference between post-stem-cell stages overall and stem-cell spermatogonia was smaller than is generally found with chemicals, not only with respect to the frequency but also the nature of mutations.</description><subject>Animals</subject><subject>Cellular biology</subject><subject>Chromosome Mapping</subject><subject>Female</subject><subject>Genes, Dominant</subject><subject>Genetics</subject><subject>Germ-Line Mutation - radiation effects</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Mutation</subject><subject>Radiation</subject><subject>Rodents</subject><subject>Spermatozoa - radiation effects</subject><issn>0016-6731</issn><issn>1943-2631</issn><issn>1943-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkUFv1DAQhS0EKkvhFyAkiwOcsvXEjhNfkKotlEpbIbVwthxnsusqsRc7YcW_x2WXqnDhYo803zzNvEfIa2BLYIqfbdDj5Gw6A9EsxRIqWT8hC1CCF6Xk8JQsGANZyJrDc_IipTvGmFRVc0JOVCUZr-WChAvX9xjRT84M9AbTLviENPT0Osy5uDYD0kuMY7HCYaC3k9lgolOgN6ZzZnLBF1e-my129HaH1vXOFutg50SN7-hFGJ03fqLX8_QbTi_Js94MCV8d_1Py7dPHr6vPxfrL5dXqfF3YqpJTgdBCW1ZVbU2vFAqT654rC0qWdVu2nWQ1NMLYXItW2vyIDnshDOtqbFt-Sj4cdHdzO2Jn84HRDHoX3WjiTx2M0393vNvqTfihQcjsUpkF3h0FYvg-Y5r06JLNHhiP2Rldq0ZAqfh_QZAiazZVBt_-A96FOfrsgi5BAK_ySRniB8jGkFLE_mFlYPo-df0n9bxpo4W-Tz1PvXl87cPMMebcf3_ob91mu3cRdRrNMGQa9H6_f6T0C4BDulA</recordid><startdate>19980401</startdate><enddate>19980401</enddate><creator>Russell, W. 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source | Freely Accessible Journals; Oxford Journals Online; Alma/SFX Local Collection |
subjects | Animals Cellular biology Chromosome Mapping Female Genes, Dominant Genetics Germ-Line Mutation - radiation effects Male Mice Mice, Inbred C3H Mutation Radiation Rodents Spermatozoa - radiation effects |
title | Differential Response of Mouse Male Germ-Cell Stages to Radiation-Induced Specific-Locus and Dominant Mutations |
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