Literature DB >> 22795640

Nuclear lamin functions and disease.

Veronika Butin-Israeli1, Stephen A Adam, Anne E Goldman, Robert D Goldman.   

Abstract

Recent studies have shown that premature cellular senescence and normal organ development and function depend on the type V intermediate filament proteins, the lamins, which are major structural proteins of the nucleus. This review presents an up-to-date summary of the literature describing new findings on lamin functions in various cellular processes and emphasizes the relationship between the lamins and devastating diseases ranging from premature aging to cancer. Recent insights into the structure and function of the A- and B- type lamins in normal cells and their dysfunctions in diseased cells are providing novel targets for the development of new diagnostic procedures and disease intervention. We summarize these recent findings, focusing on data from mice and humans, and highlight the expanding knowledge of these proteins in both healthy and diseased cells.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22795640      PMCID: PMC3633455          DOI: 10.1016/j.tig.2012.06.001

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  98 in total

Review 1.  Progeria syndromes and ageing: what is the connection?

Authors:  Christopher R Burtner; Brian K Kennedy
Journal:  Nat Rev Mol Cell Biol       Date:  2010-08       Impact factor: 94.444

2.  Defective DSB repair correlates with abnormal nuclear morphology and is improved with FTI treatment in Hutchinson-Gilford progeria syndrome fibroblasts.

Authors:  Dan Constantinescu; Antonei B Csoka; Christopher S Navara; Gerald P Schatten
Journal:  Exp Cell Res       Date:  2010-06-25       Impact factor: 3.905

Review 3.  Fraying at the edge mouse models of diseases resulting from defects at the nuclear periphery.

Authors:  Tatiana V Cohen; Colin L Stewart
Journal:  Curr Top Dev Biol       Date:  2008       Impact factor: 4.897

4.  Histone H4 lysine 16 hypoacetylation is associated with defective DNA repair and premature senescence in Zmpste24-deficient mice.

Authors:  Vaidehi Krishnan; Maggie Zi Ying Chow; Zimei Wang; Le Zhang; Baohua Liu; Xinguang Liu; Zhongjun Zhou
Journal:  Proc Natl Acad Sci U S A       Date:  2011-07-11       Impact factor: 11.205

5.  Direct synthesis of lamin A, bypassing prelamin a processing, causes misshapen nuclei in fibroblasts but no detectable pathology in mice.

Authors:  Catherine Coffinier; Hea-Jin Jung; Ziwei Li; Chika Nobumori; Ui Jeong Yun; Emily A Farber; Brandon S Davies; Michael M Weinstein; Shao H Yang; Jan Lammerding; Javad N Farahani; Laurent A Bentolila; Loren G Fong; Stephen G Young
Journal:  J Biol Chem       Date:  2010-05-03       Impact factor: 5.157

6.  DNA damage responses in progeroid syndromes arise from defective maturation of prelamin A.

Authors:  Yiyong Liu; Antonio Rusinol; Michael Sinensky; Youjie Wang; Yue Zou
Journal:  J Cell Sci       Date:  2006-10-24       Impact factor: 5.285

7.  Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy.

Authors:  Pietro Guaraldi; Vincenzo Donadio; Sabina Capellari; Manuela Contin; Maria Chiara Casadio; Pasquale Montagna; Rocco Liguori; Pietro Cortelli
Journal:  Auton Neurosci       Date:  2010-08-16       Impact factor: 3.145

8.  Mammalian prenylcysteine carboxyl methyltransferase is in the endoplasmic reticulum.

Authors:  Q Dai; E Choy; V Chiu; J Romano; S R Slivka; S A Steitz; S Michaelis; M R Philips
Journal:  J Biol Chem       Date:  1998-06-12       Impact factor: 5.157

9.  The supramolecular organization of the C. elegans nuclear lamin filament.

Authors:  Kfir Ben-Harush; Naama Wiesel; Daphna Frenkiel-Krispin; Dorothee Moeller; Eyal Soreq; Ueli Aebi; Harald Herrmann; Yosef Gruenbaum; Ohad Medalia
Journal:  J Mol Biol       Date:  2008-12-16       Impact factor: 5.469

10.  The accumulation of un-repairable DNA damage in laminopathy progeria fibroblasts is caused by ROS generation and is prevented by treatment with N-acetyl cysteine.

Authors:  Shane A Richards; Joanne Muter; Pamela Ritchie; Giovanna Lattanzi; Christopher J Hutchison
Journal:  Hum Mol Genet       Date:  2011-08-01       Impact factor: 6.150

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  115 in total

Review 1.  Something silent this way forms: the functional organization of the repressive nuclear compartment.

Authors:  Joan C Ritland Politz; David Scalzo; Mark Groudine
Journal:  Annu Rev Cell Dev Biol       Date:  2013-07-05       Impact factor: 13.827

2.  Proliferation and differentiation of mouse embryonic stem cells lacking all lamins.

Authors:  Youngjo Kim; Xiaobin Zheng; Yixian Zheng
Journal:  Cell Res       Date:  2013-08-27       Impact factor: 25.617

Review 3.  NMCP/LINC proteins: putative lamin analogs in plants?

Authors:  Malgorzata Ciska; Susana Moreno Diaz de la Espina
Journal:  Plant Signal Behav       Date:  2013-10-15

4.  Nuclear lamins: making contacts with promoters.

Authors:  Eivind Lund; Philippe Collas
Journal:  Nucleus       Date:  2013-11-08       Impact factor: 4.197

5.  Neutrophil-induced genomic instability impedes resolution of inflammation and wound healing.

Authors:  Veronika Butin-Israeli; Triet M Bui; Hannah L Wiesolek; Lorraine Mascarenhas; Joseph J Lee; Lindsey C Mehl; Kaitlyn R Knutson; Stephen A Adam; Robert D Goldman; Arthur Beyder; Lisa Wiesmuller; Stephen B Hanauer; Ronen Sumagin
Journal:  J Clin Invest       Date:  2019-01-14       Impact factor: 14.808

Review 6.  When function follows form: Nuclear compartment structure and the epigenetic landscape of the aging neuron.

Authors:  Johannes C M Schlachetzki; Tomohisa Toda; Jerome Mertens
Journal:  Exp Gerontol       Date:  2020-02-14       Impact factor: 4.032

Review 7.  Lamins and Lamin-Associated Proteins in Gastrointestinal Health and Disease.

Authors:  Graham F Brady; Raymond Kwan; Juliana Bragazzi Cunha; Jared S Elenbaas; M Bishr Omary
Journal:  Gastroenterology       Date:  2018-03-13       Impact factor: 22.682

Review 8.  When lamins go bad: nuclear structure and disease.

Authors:  Katherine H Schreiber; Brian K Kennedy
Journal:  Cell       Date:  2013-03-14       Impact factor: 41.582

9.  Nuclear lamina genetic variants, including a truncated LAP2, in twins and siblings with nonalcoholic fatty liver disease.

Authors:  Graham F Brady; Raymond Kwan; Peter J Ulintz; Phirum Nguyen; Shirin Bassirian; Venkatesha Basrur; Alexey I Nesvizhskii; Rohit Loomba; M Bishr Omary
Journal:  Hepatology       Date:  2018-03-24       Impact factor: 17.425

10.  Mutation of caspase-digestion sites in keratin 18 interferes with filament reorganization, and predisposes to hepatocyte necrosis and loss of membrane integrity.

Authors:  Sujith V W Weerasinghe; Nam-On Ku; Peter J Altshuler; Raymond Kwan; M Bishr Omary
Journal:  J Cell Sci       Date:  2014-01-24       Impact factor: 5.285

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