Literature DB >> 18621876

The lamin B receptor under transcriptional control of C/EBPepsilon is required for morphological but not functional maturation of neutrophils.

Tatiana V Cohen1, Kimberly D Klarmann, Krisada Sakchaisri, Jason P Cooper, Douglas Kuhns, Miriam Anver, Peter F Johnson, Simon C Williams, Jonathan R Keller, Colin L Stewart.   

Abstract

The lamin B receptor (LBR) is an integral nuclear envelope protein that interacts with chromatin and has homology to sterol reductases. Mutations in LBR result in Pelger-Huët anomaly and HEM-Greenberg skeletal dysplasia, whereas in mice Lbr mutations result in ichthyosis. To further understand the function of the LBR and its role in disease, we derived a novel mouse model with a gene-trap insertion into the Lbr locus (Lbr(GT/GT)). Phenotypically, the Lbr(GT/GT) mice are similar to ichthyosis mice. The Lbr(GT/GT) granulocytes lack a mature segmented nucleus and have a block in late maturation. Despite these changes in nuclear morphology, the innate granulocyte immune function in the killing of Staphylococcus aureus bacteria appears to be intact. Granulocyte differentiation requires the transcription factor C/EBPepsilon. We identified C/EBPepsilon binding sites within the Lbr promoter and used EMSAs and luciferase assays to show that Lbr is transcriptionally regulated by C/EBPepsilon. Our findings indicate that the Lbr(GT/GT) mice are a model for Pelger-Huët anomaly and that Lbr, under transcriptional regulation of C/EBPepsilon, is necessary for morphological but not necessarily functional granulocyte maturation.

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Year:  2008        PMID: 18621876      PMCID: PMC2536505          DOI: 10.1093/hmg/ddn191

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  54 in total

1.  A new mathematical model for relative quantification in real-time RT-PCR.

Authors:  M W Pfaffl
Journal:  Nucleic Acids Res       Date:  2001-05-01       Impact factor: 16.971

Review 2.  Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes.

Authors:  J C Oosterwijk; S Mansour; G van Noort; H R Waterham; C M Hall; R C M Hennekam
Journal:  J Med Genet       Date:  2003-12       Impact factor: 6.318

3.  Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith--Lemli--Opitz syndrome.

Authors:  C A Wassif; P Zhu; L Kratz; P A Krakowiak; K P Battaile; F F Weight; A Grinberg; R D Steiner; N A Nwokoro; R I Kelley; R R Stewart; F D Porter
Journal:  Hum Mol Genet       Date:  2001-03-15       Impact factor: 6.150

4.  Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene.

Authors:  Hans R Waterham; Janet Koster; Petra Mooyer; Gerard van Noort Gv; Richard I Kelley; William R Wilcox; Ronald J A Wanders; Raoul C M Hennekam; Jan C Oosterwijk
Journal:  Am J Hum Genet       Date:  2003-02-28       Impact factor: 11.025

5.  Transcriptional activity of CCAAT/enhancer-binding proteins is controlled by a conserved inhibitory domain that is a target for sumoylation.

Authors:  Jinyong Kim; Carrie A Cantwell; Peter F Johnson; Curt M Pfarr; Simon C Williams
Journal:  J Biol Chem       Date:  2002-08-02       Impact factor: 5.157

6.  Pathologic, radiographic and molecular findings in three fetuses diagnosed with HEM/Greenberg skeletal dysplasia.

Authors:  Anastasia Konstantinidou; Charalampos Karadimas; Hans R Waterham; Andrea Superti-Furga; Petros Kaminopetros; Maria Grigoriadou; Haris Kokotas; George Agrogiannis; Aglaia Giannoulia-Karantana; Efstratios Patsouris; Michael B Petersen
Journal:  Prenat Diagn       Date:  2008-04       Impact factor: 3.050

7.  Structural basis for DNA recognition by the basic region leucine zipper transcription factor CCAAT/enhancer-binding protein alpha.

Authors:  Maria Miller; Jon D Shuman; Thomas Sebastian; Zbigniew Dauter; Peter F Johnson
Journal:  J Biol Chem       Date:  2003-02-10       Impact factor: 5.157

8.  Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly.

Authors:  Leonard D Shultz; Bonnie L Lyons; Lisa M Burzenski; Bruce Gott; Rebecca Samuels; Peter A Schweitzer; Christine Dreger; Harald Herrmann; Vera Kalscheuer; Ada L Olins; Donald E Olins; Karl Sperling; Katrin Hoffmann
Journal:  Hum Mol Genet       Date:  2003-01-01       Impact factor: 6.150

9.  The lipid phosphatase LPP3 regulates extra-embryonic vasculogenesis and axis patterning.

Authors:  Diana Escalante-Alcalde; Lidia Hernandez; Hervé Le Stunff; Ryu Maeda; Hyun-Shik Lee; Vicki A Sciorra; Ira Daar; Sarah Spiegel; Andrew J Morris; Colin L Stewart
Journal:  Development       Date:  2003-10       Impact factor: 6.868

10.  Cytoskeletal influences on nuclear shape in granulocytic HL-60 cells.

Authors:  Ada L Olins; Donald E Olins
Journal:  BMC Cell Biol       Date:  2004-08-19       Impact factor: 4.241

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  22 in total

1.  Altering lamina assembly reveals lamina-dependent and -independent functions for A-type lamins.

Authors:  Monika Zwerger; Heidi Roschitzki-Voser; Reto Zbinden; Celine Denais; Harald Herrmann; Jan Lammerding; Markus G Grütter; Ohad Medalia
Journal:  J Cell Sci       Date:  2015-08-14       Impact factor: 5.285

2.  A novel case of Greenberg dysplasia and genotype-phenotype correlation analysis for LBR pathogenic variants: An instructive example of one gene-multiple phenotypes.

Authors:  Elisa Giorgio; Fabio Sirchia; Martino Bosco; Nara Lygia M Sobreira; Enrico Grosso; Alessandro Brussino; Alfredo Brusco
Journal:  Am J Med Genet A       Date:  2018-12-18       Impact factor: 2.802

Review 3.  How does the royal family of Tudor rule the PIWI-interacting RNA pathway?

Authors:  Mikiko C Siomi; Taro Mannen; Haruhiko Siomi
Journal:  Genes Dev       Date:  2010-04-01       Impact factor: 11.361

4.  Genetic disruption of Smad7 impairs skeletal muscle growth and regeneration.

Authors:  Tatiana V Cohen; Helen D Kollias; Naili Liu; Christopher W Ward; Kathryn R Wagner
Journal:  J Physiol       Date:  2015-05-15       Impact factor: 5.182

5.  Congenital Pelger-Huët anomaly in a Danish/Swedish Farmdog: case report.

Authors:  Janina Lukaszewska; Robin W Allison; Julita Stepkowska
Journal:  Acta Vet Scand       Date:  2011-03-01       Impact factor: 1.695

6.  Twin enzymes, divergent control: The cholesterogenic enzymes DHCR14 and LBR are differentially regulated transcriptionally and post-translationally.

Authors:  Isabelle M Capell-Hattam; Laura J Sharpe; Lydia Qian; Gene Hart-Smith; Anika V Prabhu; Andrew J Brown
Journal:  J Biol Chem       Date:  2020-01-07       Impact factor: 5.157

Review 7.  Lamin B receptor: multi-tasking at the nuclear envelope.

Authors:  Ada L Olins; Gale Rhodes; David B Mark Welch; Monika Zwerger; Donald E Olins
Journal:  Nucleus       Date:  2010 Jan-Feb       Impact factor: 4.197

8.  Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein.

Authors:  Peter Clayton; Björn Fischer; Anuska Mann; Sahar Mansour; Eva Rossier; Markus Veen; Christine Lang; Sevjidmaa Baasanjav; Moritz Kieslich; Katja Brossuleit; Sophia Gravemann; Nele Schnipper; Mohsen Karbasyian; Ilja Demuth; Monika Zwerger; Amparo Vaya; Gerd Utermann; Stefan Mundlos; Sigmar Stricker; Karl Sperling; Katrin Hoffmann
Journal:  Nucleus       Date:  2010-05-21       Impact factor: 4.197

9.  Cooperative Activity of GABP with PU.1 or C/EBPε Regulates Lamin B Receptor Gene Expression, Implicating Their Roles in Granulocyte Nuclear Maturation.

Authors:  Krishnakumar Malu; Rahul Garhwal; Margery G H Pelletier; Deepali Gotur; Stephanie Halene; Monika Zwerger; Zhong-Fa Yang; Alan G Rosmarin; Peter Gaines
Journal:  J Immunol       Date:  2016-06-24       Impact factor: 5.422

10.  Induction of a massive endoplasmic reticulum and perinuclear space expansion by expression of lamin B receptor mutants and the related sterol reductases TM7SF2 and DHCR7.

Authors:  Monika Zwerger; Thorsten Kolb; Karsten Richter; Iakowos Karakesisoglou; Harald Herrmann
Journal:  Mol Biol Cell       Date:  2009-11-25       Impact factor: 4.138

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