A weak germ-line excision mutation blocks developmentally controlled amplification of the rDNA minichromosome of Tetrahymena thermophila.

Abstract:

:During development of the somatic macronucleus of Tetrahymena thermophila, the rDNA is excised from its germ-line chromosome, rearranged into a palindrome, and amplified to 10(4) copies. We have identified a cis-acting germ-line mutation, rmm11/6, that prevents amplification of the rDNA in all but approximately 1 in 10(5) cells when it is the only rDNA allele in the developing macronucleus. The rmm11/6 mutation resides in a conserved element required for excision, the chromosome breakage sequence (Cbs) flanking the 3' end of the rDNA. Surprisingly, the rmm11/6 mutation only weakly affects excision of the rDNA from its germ-line location; at least 25% of cells heterozygous for this mutation correctly excise the affected rDNA allele. In heterozygotes, when this rDNA allele is excised, it is also poorly amplified. The rDNA amplification defect caused by this mutation is not overcome by delaying amplification with the DNA synthesis inhibitor aphidicolin, indicating that rDNA excision and amplification are not experimentally separable. Our experiments provide the first evidence that the capacity to amplify the rDNA is restricted in the developing macronucleus. We propose that the rmm11/6 mutation delays excision of the rDNA and that the developmental progression of the macronucleus past a restricted window for amplification is responsible for the severe amplification defect caused by this weak rDNA excision mutation.

journal_name

Genes Dev

journal_title

Genes & development

authors

Kapler GM,Blackburn EH

doi

10.1101/gad.8.1.84

subject

Has Abstract

pub_date

1994-01-01 00:00:00

pages

84-95

issue

1

eissn

0890-9369

issn

1549-5477

journal_volume

8

pub_type

杂志文章
  • The loss of circadian PAR bZip transcription factors results in epilepsy.

    abstract::DBP (albumin D-site-binding protein), HLF (hepatic leukemia factor), and TEF (thyrotroph embryonic factor) are the three members of the PAR bZip (proline and acidic amino acid-rich basic leucine zipper) transcription factor family. All three of these transcriptional regulatory proteins accumulate with robust circadian...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.301404

    authors: Gachon F,Fonjallaz P,Damiola F,Gos P,Kodama T,Zakany J,Duboule D,Petit B,Tafti M,Schibler U

    更新日期:2004-06-15 00:00:00

  • Identification of the sigma E subunit of Escherichia coli RNA polymerase: a second alternate sigma factor involved in high-temperature gene expression.

    abstract::The rpoH gene of Escherichia coli encodes sigma 32, the 32-kD sigma-factor responsible for the heat-inducible transcription of the heat shock genes. rpoH is transcribed from at least three promoters. Two of these promoters are recognized by RNA polymerase containing sigma 70, the predominant sigma-factor. We purified ...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.3.9.1462

    authors: Erickson JW,Gross CA

    更新日期:1989-09-01 00:00:00

  • Identification of a new APC/C recognition domain, the A box, which is required for the Cdh1-dependent destruction of the kinase Aurora-A during mitotic exit.

    abstract::The mitotic kinase Aurora A (Aur-A) is required for formation of a bipolar mitotic spindle and accurate chromosome segregation. In somatic cells, Aur-A protein and kinase activity levels peak during mitosis, and Aur-A is degraded during mitotic exit. Here, we investigated how Aur-A protein and kinase activity levels a...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1007302

    authors: Littlepage LE,Ruderman JV

    更新日期:2002-09-01 00:00:00

  • A nonproteolytic function of the proteasome is required for the dissociation of Cdc2 and cyclin B at the end of M phase.

    abstract::Inactivation of cyclin B-Cdc2 kinase at the exit from M phase depends on the specific proteolysis of the cyclin B subunit, whereas the Cdc2 subunit remains present at nearly constant levels throughout the cell cycle. It is unknown how Cdc2 escapes degradation when cyclin B is destroyed. In Xenopus egg extracts that re...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.823200

    authors: Nishiyama A,Tachibana K,Igarashi Y,Yasuda H,Tanahashi N,Tanaka K,Ohsumi K,Kishimoto T

    更新日期:2000-09-15 00:00:00

  • CBL family E3 ubiquitin ligases control JAK2 ubiquitination and stability in hematopoietic stem cells and myeloid malignancies.

    abstract::Janus kinase 2 (JAK2) is a central kinase in hematopoietic stem/progenitor cells (HSPCs), and its uncontrolled activation is a prominent oncogenic driver of hematopoietic neoplasms. However, molecular mechanisms underlying the regulation of JAK2 have remained elusive. Here we report that the Casitas B-cell lymphoma (C...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.297135.117

    authors: Lv K,Jiang J,Donaghy R,Riling CR,Cheng Y,Chandra V,Rozenova K,An W,Mohapatra BC,Goetz BT,Pillai V,Han X,Todd EA,Jeschke GR,Langdon WY,Kumar S,Hexner EO,Band H,Tong W

    更新日期:2017-05-15 00:00:00

  • Diverse protein kinase interactions identified by protein microarrays reveal novel connections between cellular processes.

    abstract::Protein kinases are key regulators of cellular processes. In spite of considerable effort, a full understanding of the pathways they participate in remains elusive. We globally investigated the proteins that interact with the majority of yeast protein kinases using protein microarrays. Eighty-five kinases were purifie...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1998811

    authors: Fasolo J,Sboner A,Sun MG,Yu H,Chen R,Sharon D,Kim PM,Gerstein M,Snyder M

    更新日期:2011-04-01 00:00:00

  • Multipotent hematopoietic cells susceptible to alternative double-strand break repair pathways that promote genome rearrangements.

    abstract::Chromosomal translocations are a hallmark of hematopoietic malignancies. The initial molecular events or pathways that lead to translocations in hematopoietic cells are largely unknown, particularly in the stem cell-enriched population postulated to be the initial target for these events. We used in vitro differentiat...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1522807

    authors: Francis R,Richardson C

    更新日期:2007-05-01 00:00:00

  • Specific regulation of Xenopus chromosomal 5S rRNA gene transcription in vivo by histone H1.

    abstract::The incorporation of histone H1 into chromatin during embryogenesis directs the specific repression of the Xenopus oocyte 5S rRNA genes. An increase in histone H1 content specifically restricts TFIIIA-activated transcription, and a decrease in histone H1 within chromatin facilitates the activation of the oocyte 5S rRN...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.8.10.1147

    authors: Bouvet P,Dimitrov S,Wolffe AP

    更新日期:1994-05-15 00:00:00

  • The acidic activator GAL4-AH can stimulate polymerase II transcription by promoting assembly of a closed complex requiring TFIID and TFIIA.

    abstract::The assembly of activated RNA polymerase II (pol II) transcription complexes has been investigated by assaying whether pre-assembly of intermediate complexes reduces the extended time required for start-site melting. The results show that a closed complex requiring factors IIA, IID, and the acidic activator GAL4-AH fo...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.6.9.1716

    authors: Wang W,Gralla JD,Carey M

    更新日期:1992-09-01 00:00:00

  • Glucose regulates protein interactions within the yeast SNF1 protein kinase complex.

    abstract::The SNF1 protein kinase is broadly conserved in eukaryotes and has been implicated in responses to environmental and nutritional stress. In yeast, the SNF1 kinase has a central role in the response to glucose starvation. SNF1 is associated with its activating subunit, SNF4, and other proteins in complexes. Using the t...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.10.24.3105

    authors: Jiang R,Carlson M

    更新日期:1996-12-15 00:00:00

  • Life on the edge: telomeres and persistent DNA breaks converge at the nuclear periphery.

    abstract::Persistent DNA double-strand breaks and telomeres represent genomic hazards, as they can instigate inappropriate repair reactions. Two recent papers by Oza and colleagues (pp. 912-917) and Schober and colleagues (pp. 928-938) show that both types of DNA ends are sequestered from bulk DNA by Mps3, a SUN domain protein ...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1805309

    authors: Gartenberg MR

    更新日期:2009-05-01 00:00:00

  • The interplay between multiple enhancer and silencer elements defines the pattern of decapentaplegic expression.

    abstract::The product of the zygotically active decapentaplegic (dpp) gene appears to function as a morphogen that specifies positional information in the dorsal half of the Drosophila embryo. The dorsal-specific transcription of dpp is the key step in establishing a morphogen gradient. We demonstrate here that multiple regions...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.7.4.694

    authors: Huang JD,Schwyter DH,Shirokawa JM,Courey AJ

    更新日期:1993-04-01 00:00:00

  • Hedgehog signaling and the retina: insights into the mechanisms controlling the proliferative properties of neural precursors.

    abstract::Hedgehog signaling has been linked to cell proliferation in a variety of systems; however, its effects on the cell cycle have not been closely studied. In the vertebrate retina, Hedgehog's effects are controversial, with some reports emphasizing increased proliferation and others pointing to a role in cell cycle exit....

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.391106

    authors: Locker M,Agathocleous M,Amato MA,Parain K,Harris WA,Perron M

    更新日期:2006-11-01 00:00:00

  • Psidin, a conserved protein that regulates protrusion dynamics and cell migration.

    abstract::Dynamic assembly and disassembly of actin filaments is a major driving force for cell movements. Border cells in the Drosophila ovary provide a simple and genetically tractable model to study the mechanisms regulating cell migration. To identify new genes that regulate cell movement in vivo, we screened lethal mutatio...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.2028611

    authors: Kim JH,Cho A,Yin H,Schafer DA,Mouneimne G,Simpson KJ,Nguyen KV,Brugge JS,Montell DJ

    更新日期:2011-04-01 00:00:00

  • Recruitment of Thr 319-phosphorylated Ndd1p to the FHA domain of Fkh2p requires Clb kinase activity: a mechanism for CLB cluster gene activation.

    abstract::Activation of the CLB gene cluster through the assembly of Mcm1p-Fkh2p complexes at target promoters is essential for mitotic entry and transition through M phase. We show that the activation of this mitotic transcriptional program is dependent on the recruitment of Ndd1p, a coactivator that performs its essential fun...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1074103

    authors: Reynolds D,Shi BJ,McLean C,Katsis F,Kemp B,Dalton S

    更新日期:2003-07-15 00:00:00

  • Establishment of ventral cell fates in the Drosophila embryonic ectoderm requires DER, the EGF receptor homolog.

    abstract::The embryonic ectoderm in Drosophila displays a highly organized arrangement of specific structures along the dorsal-ventral axis. To establish this characteristic design, cells must receive instructive cues regarding their position. We present evidence that during stages 8-9 of embryonic development, the Drosophila E...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.7.10.1937

    authors: Raz E,Shilo BZ

    更新日期:1993-10-01 00:00:00

  • Targeting Argonaute to chromatin.

    abstract::In many eukaryotes, siRNAs bound to Argonaute proteins guide chromatin-modifying enzymes to complementary loci, resulting in transcriptional gene silencing. Multiple lines of evidence indicate that siRNAs base-pair with longer RNAs produced at target loci, but the possibility that siRNAs base-pair directly with DNA re...

    journal_title:Genes & development

    pub_type: 评论,杂志文章

    doi:10.1101/gad.294900.116

    authors: Wendte JM,Pikaard CS

    更新日期:2016-12-15 00:00:00

  • Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

    abstract::Disruptions in the use of skeletal muscle lead to muscle atrophy. After short periods of disuse, muscle atrophy is reversible, and even after prolonged periods of inactivity, myofiber degeneration is uncommon. The pathways that regulate atrophy, initiated either by peripheral nerve damage, immobilization, aging, catab...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1318305

    authors: Wang X,Blagden C,Fan J,Nowak SJ,Taniuchi I,Littman DR,Burden SJ

    更新日期:2005-07-15 00:00:00

  • Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications.

    abstract::Genome integrity is constantly monitored by sophisticated cellular networks, collectively termed the DNA damage response (DDR). A common feature of DDR proteins is their mobilization in response to genotoxic stress. Here, we outline how the development of various complementary methodologies has provided valuable insig...

    journal_title:Genes & development

    pub_type: 杂志文章,评审

    doi:10.1101/gad.2021311

    authors: Polo SE,Jackson SP

    更新日期:2011-03-01 00:00:00

  • Reelin-induced tyrosine [corrected] phosphorylation of disabled 1 during neuronal positioning.

    abstract::The reelin (reln) and disabled 1 (dab1) genes both ensure correct neuronal positioning during brain development. We have found that the intracellular Dab1 protein receives a tyrosine phosphorylation signal from extracellular Reln protein. Genetic analysis shows that reln function depends on dab1, and vice versa, as ex...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.13.6.643

    authors: Howell BW,Herrick TM,Cooper JA

    更新日期:1999-03-15 00:00:00

  • Maternal Eed knockout causes loss of H3K27me3 imprinting and random X inactivation in the extraembryonic cells.

    abstract::Genomic imprinting is essential for mammalian development. Recent studies have revealed that maternal histone H3 Lys27 trimethylation (H3K27me3) can mediate DNA methylation-independent genomic imprinting. However, the regulatory mechanisms and functions of this new imprinting mechanism are largely unknown. Here we dem...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.318675.118

    authors: Inoue A,Chen Z,Yin Q,Zhang Y

    更新日期:2018-12-01 00:00:00

  • DTL/CDT2 is essential for both CDT1 regulation and the early G2/M checkpoint.

    abstract::Checkpoint genes maintain genomic stability by arresting cells after DNA damage. Many of these genes also control cell cycle events in unperturbed cells. By conducting a screen for checkpoint genes in zebrafish, we found that dtl/cdt2 is an essential component of the early, radiation-induced G2/M checkpoint. We subseq...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1482106

    authors: Sansam CL,Shepard JL,Lai K,Ianari A,Danielian PS,Amsterdam A,Hopkins N,Lees JA

    更新日期:2006-11-15 00:00:00

  • BRCA1/BARD1 inhibition of mRNA 3' processing involves targeted degradation of RNA polymerase II.

    abstract::Mammalian cells exhibit a complex response to DNA damage. The tumor suppressor BRCA1 and associated protein BARD1 are thought to play an important role in this response, and our previous work demonstrated that this includes transient inhibition of the pre-mRNA 3' processing machinery. Here we provide evidence that thi...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1309505

    authors: Kleiman FE,Wu-Baer F,Fonseca D,Kaneko S,Baer R,Manley JL

    更新日期:2005-05-15 00:00:00

  • Coregulation of anterior and posterior mesendodermal development by a hairy-related transcriptional repressor.

    abstract::During embryonic development in vertebrates, the endoderm becomes patterned along the anteroposterior axis to produce distinct derivatives. How this regulation is controlled is not well understood. We report that the zebrafish hairy/enhancer of split [E(spl)]-related gene her5 plays a critical role in this process. At...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:

    authors: Bally-Cuif L,Goutel C,Wassef M,Wurst W,Rosa F

    更新日期:2000-07-01 00:00:00

  • A Slicer-independent role for Argonaute 2 in hematopoiesis and the microRNA pathway.

    abstract::Binding of microRNA (miRNA) to mRNA within the RNA-induced silencing complex (RISC) leads to either translational inhibition or to destruction of the target mRNA. Both of these functions are executed by Argonaute 2 (Ago2). Using hematopoiesis in mice as a model system to study the physiological function of Ago2 in viv...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1565607

    authors: O'Carroll D,Mecklenbrauker I,Das PP,Santana A,Koenig U,Enright AJ,Miska EA,Tarakhovsky A

    更新日期:2007-08-15 00:00:00

  • A novel class of small RNAs in mouse spermatogenic cells.

    abstract::Small noncoding RNAs, including small interfering RNAs (siRNAs) and micro RNAs (miRNAs) of approximately 21 nucleotides (nt) in length, have emerged as potent regulators of gene expression at both transcriptional and post-transcriptional levels in diverse organisms. Here we report the identification of a novel class o...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1434406

    authors: Grivna ST,Beyret E,Wang Z,Lin H

    更新日期:2006-07-01 00:00:00

  • A splicing enhancer exhibits both constitutive and regulated activities.

    abstract::The Drosophila proteins Transformer (Tra) and Transformer2 (Tra2) regulate the sex-specific alternative splicing of Drosophila doublesex (dsx) pre-mRNA by specifically binding to a splicing enhancer (dsx repeat element; dsxRE) located 300 nucleotides (nt) downstream from a female-specific 3' splice site. In this paper...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.8.14.1703

    authors: Tian M,Maniatis T

    更新日期:1994-07-15 00:00:00

  • A PDK1 homolog is necessary and sufficient to transduce AGE-1 PI3 kinase signals that regulate diapause in Caenorhabditis elegans.

    abstract::An insulin receptor-like signaling pathway regulates Caenorhabditis elegans metabolism, development, and longevity. Inactivation of the insulin receptor homolog DAF-2, the AGE-1 PI3K, or the AKT-1 and AKT-2 kinases causes a developmental arrest at the dauer stage. A null mutation in the daf-16 Fork head transcription ...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.13.11.1438

    authors: Paradis S,Ailion M,Toker A,Thomas JH,Ruvkun G

    更新日期:1999-06-01 00:00:00

  • H3.3 actively marks enhancers and primes gene transcription via opening higher-ordered chromatin.

    abstract::The histone variants H3.3 and H2A.Z have recently emerged as two of the most important features in transcriptional regulation, the molecular mechanism of which still remains poorly understood. In this study, we investigated the regulation of H3.3 and H2A.Z on chromatin dynamics during transcriptional activation. Our i...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.222174.113

    authors: Chen P,Zhao J,Wang Y,Wang M,Long H,Liang D,Huang L,Wen Z,Li W,Li X,Feng H,Zhao H,Zhu P,Li M,Wang QF,Li G

    更新日期:2013-10-01 00:00:00

  • A conserved ncRNA-binding protein recruits silencing factors to heterochromatin through an RNAi-independent mechanism.

    abstract::Long noncoding RNAs (lncRNAs) can trigger repressive chromatin, but how they recruit silencing factors remains unclear. In Schizosaccharomyces pombe, heterochromatin assembly on transcribed noncoding pericentromeric repeats requires both RNAi and RNAi-independent mechanisms. In Saccharomyces cerevisiae, which lacks a ...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.226019.113

    authors: Marina DB,Shankar S,Natarajan P,Finn KJ,Madhani HD

    更新日期:2013-09-01 00:00:00