Malavi T. Madireddi , James F. Smothers , C. David Allis
{"title":"Waste not, want not: Does DNA elimination fuel gene amplification during development in ciliates?","authors":"Malavi T. Madireddi , James F. Smothers , C. David Allis","doi":"10.1016/S1044-5781(06)80072-1","DOIUrl":null,"url":null,"abstract":"<div><p>The sexual phase of the life cycle in ciliates represents a developmental program with several parallels to multicellular development. During this pathway an undifferentiated zygotic nucleus gives rise to two lineages, a germinal micronuclear lineage and a somatic macronuclear lineage. The development of nascent macronuclei (or ‘anlagen’) from micronuclei involves a highly regulated set of DNA rearrangements which include chromosomal breakage, telomere addition, DNA elimination and gene amplification. Here we review recent progress in identifying stage-specific polypeptides from <em>Tetrahymena</em> analgen that are likely to be involved in these rearrangements. One of the more abundant of these polypeptides, p65, participates in the formation of DNA-containing structures that resemble developing nucleoli. We propose a simple model in which the micronuclear gene segments that are not to be included in the mature macronuclear genome are first digested in these p65-based particles, and then the resulting nucleotides are ‘recycled’ by using them to amplify rDNA. Our ‘intranuclear recycling’ model suggests a possible compartmentalization strategy that functions to ensure adequate rDNA/rRNA production during macronuclear development. Implications of the model for programmed DNA rearrangements and nucleolar biogenesis are discussed.</p></div>","PeriodicalId":101155,"journal":{"name":"Seminars in Developmental Biology","volume":"6 5","pages":"Pages 305-315"},"PeriodicalIF":0.0000,"publicationDate":"1995-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1044-5781(06)80072-1","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Seminars in Developmental Biology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1044578106800721","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
Abstract
The sexual phase of the life cycle in ciliates represents a developmental program with several parallels to multicellular development. During this pathway an undifferentiated zygotic nucleus gives rise to two lineages, a germinal micronuclear lineage and a somatic macronuclear lineage. The development of nascent macronuclei (or ‘anlagen’) from micronuclei involves a highly regulated set of DNA rearrangements which include chromosomal breakage, telomere addition, DNA elimination and gene amplification. Here we review recent progress in identifying stage-specific polypeptides from Tetrahymena analgen that are likely to be involved in these rearrangements. One of the more abundant of these polypeptides, p65, participates in the formation of DNA-containing structures that resemble developing nucleoli. We propose a simple model in which the micronuclear gene segments that are not to be included in the mature macronuclear genome are first digested in these p65-based particles, and then the resulting nucleotides are ‘recycled’ by using them to amplify rDNA. Our ‘intranuclear recycling’ model suggests a possible compartmentalization strategy that functions to ensure adequate rDNA/rRNA production during macronuclear development. Implications of the model for programmed DNA rearrangements and nucleolar biogenesis are discussed.