- Open Access
The nuclear envelopathies and human diseases
© Chi et al; licensee BioMed Central Ltd. 2009
Received: 12 October 2009
Accepted: 22 October 2009
Published: 22 October 2009
The nuclear envelope (NE) consists of two membrane layers that segregate the nuclear from the cytoplasmic contents. Recent progress in our understanding of nuclear-lamina associated diseases has revealed intriguing connections between the envelope components and nuclear processes. Here, we review the functions of the nuclear envelope in chromosome organization, gene expression, DNA repair and cell cycle progression, and correlate deficiencies in envelope function with human pathologies.
The nuclear envelope (NE) is a specialized structure composed of two lipid membranes that separate the cytoplasm from the nucleoplasm. The outer nuclear membrane (ONM), studded with ribosomes, is an extension of the rough ER while the inner nuclear membrane (INM) contacts chromatin and the nuclear lamina, a type V intermediate filament that composes the nuclear skeleton . Although the NE encapsulates chromatin, it is not a uniformly closed barrier. Rather, it has several "doors" represented by the nuclear pore complexes (NPC) that allow communication between the nucleus and the cytoplasm .
NE-associated human diseases
Many human diseases are associated with NE protein defects . For example, a comprehensive proteomic study identified 13 known and 67 putative INM proteins, 23 of these proteins map to chromosome regions linked to a variety of dystrophies including congenital muscular dystrophy, Charcot-Marie-Tooth diseases and myotubular myopathy .
Diseases caused by mutations in nuclear envelope proteins.
Hutchinson-Gilford progeria syndrome
Deleted 50 a.a. at carboxyl terminal
Atypical Werner syndrome
A57P, R133L, L140R
Emery-Dreifuss muscular dystrophy, type 2
Emery-Dreifuss muscular dystrophy, type 3
Limb-gridle muscular dystrophy type 1B
Dilated cardiomyopathy, type 1A
missense mutations in exons 1 or 3
Charcot-Marie-Tooth disorder type 2B1
Familial partial lipodystrophy, Dunnigan type
missense mutations in exons 8 and 11
R527H, K542N, A529V, R527C/R471C
partial loss of exon 11
R133L and T10I
X-linked Emery-Dreifuss muscular dystrophy
S54F, P183T, P183H, Del95-99, Del236-241
Lamin B receptor
Of the laminopathies, HGPS is one of the more severe syndromes with affected individuals having a mean life span of approximately 13 years. More than 90% of HGPS are caused by a silent mutation (GGC>GGT; G608G) which leads to a mis-spliced form of Lamin A that is deleted for 50 amino acids at its C terminus. This mutated form of lamin A is termed "Progerin" . Patients expressing Progerin have aging-like features such as alopecia, sclerosis, wrinkling and arteriosclerosis at a prematurely early age .
Mutations in NE proteins Emerin or Lamin A/C may cause Emery-Dreifuss muscular dystrophy (EDMD; Table 1). EDMD is characterized by slowly progressive skeletal muscle wasting of the shoulder girdle and distal leg muscles, early contractures of the elbows and Achilles tendons, and cardiomyopathy with atrial ventricular block which eventually results in death [10, 11].
The Lamin B receptor (LBR), a member of the sterol reductase family, is evolutionarily conserved and integral to the inner nuclear membrane. LBR targets heterochromatin and lamin proteins to the nuclear membrane. Mutations in LBR cause the Pelger-Huët anomaly (PHA), an autosomal dominant disorder characterized by abnormal nuclear shape and chromatin disorganization in blood granulocytes (Table 1). Affected individuals show hypolobulated neutrophil nuclei with rough chromatin. Presumptively homozygous individuals have ovoid neutrophil nuclei, as well as varying degrees of developmental delay, epilepsy, and skeletal abnormalities .
Mouse models of nuclear envelopathies
Mouse models have been generated recently to investigate the biological relevance of different NE genes. Animals from most of these models exhibit developmental retardation and tissue-specific defects. Below, we enumerate the various mouse phenotypes that emerge from deficiencies in various NE components.
Mouse models for nuclear lamins
Mammalian somatic cells express three types of lamins, Lamin A (LMNA), Lamin B (LMNB) and Lamin C (LMNC). Lamin A and Lamin C are splicing variants that are identical in their first 566 residues, but are distinct at their carboxyl-terminal ends. The expression of Lamin A/C is tissue-specific and developmentally regulated, whereas the Lamin B protein is ubiquitously expressed in all mammalian tissues . In the mouse, A-type lamins do not appear until midway through embryonic development, suggesting that these proteins may be involved in regulating terminal differentiation. Mutations in LMNA directly affect the nuclear morphology as observed in human laminopathies . Indeed, knock out of Lmna in mice disturbs the actin, vimentin and tubulin-based cytoskeletal filamentous networks in Lmna-/- mouse embryonic fibroblasts . Although Lmna-/- mice are born as animals grossly indistinguishable from their wild type littermates, they soon display pathologies such as cardiomyopathies, lipodystrophies, alopecia and distinct scoliosis/kyphosis . It has been reported that all Lmna-/- mice perish by the eighth week after birth . Interestingly, Fong et al. showed that Lmna LCO / LCO mice which produce Lamin C but no Lamin A or prelamin A are entirely healthy, and Lmna LCO / LCO cells displayed normal Emerin localization and exhibited only minimal alterations in nuclear shape and nuclear deformability . On the other hand, mice carrying an autosomal recessive mutation in the Lamin A gene display HGPS-like pathological defects in bone, muscle and skin and death by 4 weeks of age . Thus, prelamin A and Lamin A seem to be dispensable in mice; the symptoms in laminopathies may due to the dominant negative effect of the Lamin A mutant proteins.
Although spontaneous mutations in B-type lamins have never been identified in humans or in experimental animals, the Lamin B1 mutant mice may provide evidence for a broad and non-redundant function of Lamin B1 in mammalian development. Lamin B1 is expressed in embryos and differentiated cells; homozygous Lmnb1 mutant mice live until birth, albeit with bone and lung abnormalities . Fibroblasts from mutant embryos grow under standard cell-culture conditions, but display grossly misshapen nuclei, impaired differentiation, increased ploidy, and premature senescence .
Mouse models for INM genes
Most of the known INM proteins are associated with the nuclear lamina . Several mouse models have been established to investigate the physiological consequences of a loss of interaction between the nuclear lamina and the INM proteins.
The mammalian SUN-domain proteins are inserted into the INM with their N-termini interacting with Lamin A and their C-termini connecting to the cytoplasmic architecture through direct interactions with Nesprin [20–22]. The SUN domain proteins have various functions in eukaryotic cells. The Schizosaccharomyces pombe SUN-domain protein Sad1p is a constituent of the spindle pole body (SPB) which contacts the telomere complex . Mps3p, the single SUN-domain protein in Saccharomyces cerevisiae, is required for NE anchorage-dependent recombinational repair of double-stranded DNA breaks [24, 25]. On the other hand, the C. elegans SUN-domain protein Unc-84 is required for nuclear migration and anchorage . In mice, knock out of the Sun1 alleles does not appear to affect birth or a normal life span. However, Sun1-/- animals are reproductively infertile [27, 28]. It was noted that mouse Sun1 specifically associates with telomeres during the leptotene and diplotene stages of meiotic prophase I. Knock out of Sun1 in mice impairs telomere attachment to the nuclear envelope, resulting in persistent double-strand breaks and inefficient homologous pairing and synapsis formation in meiosis [27, 28]. Moreover, Sun1-/- spermatocytes show repressed expression of reproductive genes and have no detectable piRNA . Unlike Sun1-/- animals, mice knocked out for Sun2 do not present with apparent abnormalities and are reproductively normal . On the other hand, mice deficient for both Sun1 and Sun2 die at birth and show destructive myonuclear positioning in the syncytial skeletal muscle cells . These findings establish a non-redundant role for Sun1 in tethering telomeres to the NE and in gene expression.
Lamin B receptor
The human PHA disease caused by mutation in the Lamin B receptor (LBR) gene is modeled by the ichthyosis (ic) mice. Frameshift mutations in the ic locus (1088insCC and 1884insGGAA) within the Lbr gene lead to marked abnormalities in nuclear heterochromatin. Mice homozygous for deleterious alleles at the ic locus develop abnormalities including alopecia, variable expression of syndactyly and hydrocephalus and present blood phenotype similar to PHA .
Lamin-associated polypeptide 2α (Lap2α) is a chromatin-associated protein that binds A-type lamins. The Lap2α deficient mouse model shows that Lap2α is required for nucleoplasmic localization of Lamin A. Loss of Lap2α-Lamin A interaction impairs pRb-mediated regulation of progenitor cell proliferation, leading to inefficient cell-cycle arrest in dense fibroblast cultures and the hyperproliferation of epidermal and erythroid progenitor cells in vivo .
Mouse models for NPC (nuclear pore complex)
In addition to significant changes in the nuclear shape, the Hutchinson-Gilford progeria syndrome (HGPS) is associated with prominent clustering of nuclear pores . While the link between spatial distribution of nuclear pores and a premature aging phenotype remains to be elucidated, recent findings in mouse models suggest that NPCs have additional functions in chromatin organization, gene regulation and cell cycle progression which are independent of the roles they play in nuclear transport . Below, we survey mouse data on the involvement of the nuclear pore proteins in protecting chromosomal integrity.
The nuclear pore complex disassembles and reassembles together with the nuclear envelope during cell division. How post-mitotic nuclear envelope reformation affects interphase chromatin organization is largely unknown . When disassembled, many of the nuclear pore proteins appear not to be degraded, but are recruited instead to kinetochores. These kinetochore-associated nucleoporins participate in the activity of the spindle assembly checkpoint. For example, the RNA export 1 (RAE1)-NUP98 complex is involved in RNA export in interphase. In mitosis, RAE1 binds to microtubules and is required for spindle formation . The Rae1+/-Nup98+/- compound mice show premature securin degradation, leading to precocious anaphase onset and aneuploidy . In another study, double haploinsufficiency in the mitotic checkpoint genes Bub3 and Rae1 appear to be causal of several aging-associated phenotypes . Mouse embryonic fibroblasts (MEFs) from Bub3+/-Rae1+/- mice show premature senescence and accumulate high levels of p19, p53, p21, and p16 . These results link the mitotic checkpoint gene with nucleoporins in regulating chromosome integrity, cellular senescence, and aging.
Nuclear pore associated proteins, Mad1/Mad2
The mitotic arrest deficient protein 1 (MAD1) and 2 (MAD2) are required for the faithful bipolar attachment of the mitotic spindles to kinetochores. MAD1 and MAD2 associate with NPC in interphase [37, 38]. As the nuclear membrane commences breakdown in mitosis, MAD1 and MAD2 translocate to the kinetochores via a polo-kinase dependent activity [39, 40]. In mice, the homozygous knock out of either Mad1 or Mad2 is embryonic lethal [41, 42]. Mice that are heterozygously insufficient for either Mad1 (i.e. Mad1+/-)or Mad2 (i.e. Mad2+/-) show a higher proclivity than wild type mice in developing tumors [41, 42]. In the setting of a p53+/- background, there is some evidence that Mad1+/-p53+/-, Mad2+/-p53+/-, and Mad1+/-Mad2+/-p53+/- mice have more frequent presentation per mouse of multiple independent primary tumors of different tissue types [43, 44]. The findings suggest that simultaneous loss of the Mad1/Mad2 spindle assembly checkpoint (SAC), which is often targeted by oncogenic viruses , and the p53 checkpoint holds a worse prognosis in mice for the development of multiple independent tumors in different tissues than the singular loss of either the SAC or the p53 checkpoint.
The influence of the NE on chromosome organization and gene expression
The eukaryotic genome is tightly compacted to fit into the confines of the nucleus. Accumulating evidence agree that the three-dimensional distribution of the chromosomes in the nucleus is nonrandom and falls into "territories" [46, 47]. Thus, the transcriptional state of genes may be dictated by how they are positioned and distributed in different nuclear space . Based on electron microscopic findings, the nuclear periphery was initially thought to be occupied by transcriptionally silent heterochromatin. Recent evidence, however, suggests that the association of chromatin with the NE can result in gene activation . Thus, in yeast, transcriptional activation correlates with chromatin association to NPCs, and the activation of certain genes often results in their dynamic relocation to the nuclear periphery [49–51]. In some respects, it is biologically parsimonious that gene transcription occurs at the nuclear periphery because the synthesized mRNA can then be readily exported through the nuclear pores. On the other hand, genome-wide analysis in Drosophila cells has also revealed clusters of transcriptionally silent and hypo-acetylated genes that interact with Lamin B1 and are positioned at the nuclear periphery . Using three-dimensional DNA-immuno-FISH, Reddy et al. demonstrated that an Emerin, Lamin A, Lamin B and LAP2 complex can result in establishing a distinctively repressive chromatin structure that silences transcription . Within this complex, proteins like LAP2 recruits histone deacetylases like HDAC3, causing deacetylation of histone H4 leading to transcriptional repression . In distinction with LAP2, the human SUN-domain protein 1 appears to recruit a histone acetyltransferase that acts to regulate chromatin decondensation . Collectively, the findings suggest that NE and NE-associated proteins can recruit chromatin and regulatory factors that either activate or inactivate gene transcription. In instances of aberrant loss of heterochromatin regulation, this finding is often pathologically associated with prematurely aging HGPS cells .
NE and DNA repair
The mitotic role of NE proteins
At the conclusion of mitosis as the NE reforms, the NE protein complex associates with discrete regions of mitotic chromatin in a sequential manner (Fig. 3). LAP2 and a subfraction of BAF form defined complexes in chromatin core regions [20, 61]. SUN1 and a subset of nucleoporins wrap the lateral margins of newly separated sister chromatids (Fig. 3). The nuclear lamina and Emerin then coalesce with SUN1 and LAP2 in telophase . Thus, chromatin-interacting membrane proteins such as LBR, MAN1, LAP2, and the trans-membrane nucleoporins Ndc1 and POM121 collaborate to rapidly reestablish the nuclear compartment at the end of mitosis and facilitate NE reformation . In the newly reformed nucleus, the SUN1 protein recruits a membrane associated histone acetyltransferase hALP to acetylate histones to decondense the DNA, thereby preparing the cell for transcription during the next interphase . The complexity of these events underscores the importance of nuclear envelope physiology to the normal life cycle of the cell and explains why envelope defects lead to significant diseases.
Here, we review in brief the pleiotropic functions of NE and NE-associated proteins in normal and pathological physiology. Based on extant data, it is clear that defects in NE-associated proteins can manifest as devastating diseases such as the progeroid syndromes. What is less clear is whether the syndromes occur due to a loss of a normal function (i.e. Lamin A mutation) or a gain of an abnormal dominant negative activity (i.e. expression of a mutant Progerin protein) or both. Going forward, the study of envelopathies and laminopathies may reveal balanced contributions from both losses and gains in functions to disease development. While NE proteins were originally thought to serve only simple structural roles, much more remain to be discovered about these factors for their complex regulatory functions.
Work in the authors' laboratories was supported in part by NIAID/NIH intramural funds, by the Intramural AIDS Targeted Anti-viral Program (IATAP), and by intramural grants to Y.-H.C. from the National Health Research Institutes, Taiwan (NHRI 98A1-CSPP14-014), and National Science Council, Taiwan (NSC 98-2320-B-400-009-MY3).
- Guttinger S, Laurell E, Kutay U: Orchestrating nuclear envelope disassembly and reassembly during mitosis. Nat Rev Mol Cell Biol. 2009, 10: 178-191. 10.1038/nrm2641.View ArticlePubMedGoogle Scholar
- Capelson M, Hetzer MW: The role of nuclear pores in gene regulation, development and disease. EMBO Rep. 2009, 10: 697-705. 10.1038/embor.2009.147.PubMed CentralView ArticlePubMedGoogle Scholar
- Taddei A, Hediger F, Neumann FR, Gasser SM: The Function of Nuclear Architecture: A Genetic Approach. Annu Rev Genet. 2004, 38: 305-345. 10.1146/annurev.genet.37.110801.142705.View ArticlePubMedGoogle Scholar
- Nalepa G, Harper JW: Visualization of a highly organized intranuclear network of filaments in living mammalian cells. Cell Motil Cytoskeleton. 2004, 59: 94-108. 10.1002/cm.20023.View ArticlePubMedGoogle Scholar
- Worman HJ, Fong LG, Muchir A, Young SG: Laminopathies and the long strange trip from basic cell biology to therapy. J Clin Invest. 2009, 119: 1825-1836. 10.1172/JCI37679.PubMed CentralView ArticlePubMedGoogle Scholar
- Schirmer EC, Florens L, Guan T, Yates JR, Gerace L: Nuclear membrane proteins with potential disease links found by subtractive proteomics. Science. 2003, 301: 1380-1382. 10.1126/science.1088176.View ArticlePubMedGoogle Scholar
- Capell BC, Collins FS: Human laminopathies: nuclei gone genetically awry. Nat Rev Genet. 2006, 7: 940-952. 10.1038/nrg1906.View ArticlePubMedGoogle Scholar
- Worman HJ, Courvalin JC: How do mutations in lamins A and C cause disease?. J Clin Invest. 2004, 113: 349-351.PubMed CentralView ArticlePubMedGoogle Scholar
- Merideth MA, Gordon LB, Clauss S, Sachdev V, Smith AC, Perry MB, Brewer CC, Zalewski C, Kim HJ, Solomon B: Phenotype and course of Hutchinson-Gilford progeria syndrome. N Engl J Med. 2008, 358: 592-604. 10.1056/NEJMoa0706898.PubMed CentralView ArticlePubMedGoogle Scholar
- Ellis JA: Emery-Dreifuss muscular dystrophy at the nuclear envelope: 10 years on. Cell Mol Life Sci. 2006, 63: 2702-2709. 10.1007/s00018-006-6247-8.View ArticlePubMedGoogle Scholar
- Manilal S, Nguyen TM, Sewry CA, Morris GE: The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein. Hum Mol Genet. 1996, 5: 801-808. 10.1093/hmg/5.6.801.View ArticlePubMedGoogle Scholar
- Hoffmann K, Dreger CK, Olins AL, Olins DE, Shultz LD, Lucke B, Karl H, Kaps R, Muller D, Vaya A: Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huet anomaly). Nat Genet. 2002, 31: 410-414.PubMedGoogle Scholar
- Prokocimer M, Margalit A, Gruenbaum Y: The nuclear lamina and its proposed roles in tumorigenesis: projection on the hematologic malignancies and future targeted therapy. J Struct Biol. 2006, 155: 351-360. 10.1016/j.jsb.2006.02.016.View ArticlePubMedGoogle Scholar
- Nagano A, Arahata K: Nuclear envelope proteins and associated diseases. Curr Opin Neurol. 2000, 13: 533-539. 10.1097/00019052-200010000-00005.View ArticlePubMedGoogle Scholar
- Sullivan T, Escalante-Alcalde D, Bhatt H, Anver M, Bhat N, Nagashima K, Stewart CL, Burke B: Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy. J Cell Biol. 1999, 147: 913-920. 10.1083/jcb.147.5.913.PubMed CentralView ArticlePubMedGoogle Scholar
- Fong LG, Ng JK, Lammerding J, Vickers TA, Meta M, Cote N, Gavino B, Qiao X, Chang SY, Young SR: Prelamin A and lamin A appear to be dispensable in the nuclear lamina. J Clin Invest. 2006, 116: 743-752. 10.1172/JCI27125.PubMed CentralView ArticlePubMedGoogle Scholar
- Mounkes LC, Kozlov S, Hernandez L, Sullivan T, Stewart CL: A progeroid syndrome in mice is caused by defects in A-type lamins. Nature. 2003, 423: 298-301. 10.1038/nature01631.View ArticlePubMedGoogle Scholar
- Vergnes L, Peterfy M, Bergo MO, Young SG, Reue K: Lamin B1 is required for mouse development and nuclear integrity. Proc Natl Acad Sci USA. 2004, 101: 10428-10433. 10.1073/pnas.0401424101.PubMed CentralView ArticlePubMedGoogle Scholar
- Vlcek S, Foisner R: A-type lamin networks in light of laminopathic diseases. Biochim Biophys Acta. 2007, 1773: 661-674. 10.1016/j.bbamcr.2006.07.002.View ArticlePubMedGoogle Scholar
- Chi YH, Haller K, Peloponese JM, Jeang KT: Histone acetyltransferase hALP and nuclear membrane protein hsSUN1 function in de-condensation of mitotic chromosomes. J Biol Chem. 2007, 282: 27447-27458. 10.1074/jbc.M703098200.View ArticlePubMedGoogle Scholar
- Crisp M, Liu Q, Roux K, Rattner JB, Shanahan C, Burke B, Stahl PD, Hodzic D: Coupling of the nucleus and cytoplasm: role of the LINC complex. J Cell Biol. 2006, 172: 41-53. 10.1083/jcb.200509124.PubMed CentralView ArticlePubMedGoogle Scholar
- Padmakumar VC, Libotte T, Lu W, Zaim H, Abraham S, Noegel AA, Gotzmann J, Foisner R, Karakesisoglou I: The inner nuclear membrane protein Sun1 mediates the anchorage of Nesprin-2 to the nuclear envelope. J Cell Sci. 2005, 118: 3419-3430. 10.1242/jcs.02471.View ArticlePubMedGoogle Scholar
- Chikashige Y, Tsutsumi C, Yamane M, Okamasa K, Haraguchi T, Hiraoka Y: Meiotic proteins bqt1 and bqt2 tether telomeres to form the bouquet arrangement of chromosomes. Cell. 2006, 125: 59-69. 10.1016/j.cell.2006.01.048.View ArticlePubMedGoogle Scholar
- Schober H, Ferreira H, Kalck V, Gehlen LR, Gasser SM: Yeast telomerase and the SUN domain protein Mps3 anchor telomeres and repress subtelomeric recombination. Genes Dev. 2009, 23: 928-938. 10.1101/gad.1787509.PubMed CentralView ArticlePubMedGoogle Scholar
- Oza P, Jaspersen SL, Miele A, Dekker J, Peterson CL: Mechanisms that regulate localization of a DNA double-strand break to the nuclear periphery. Genes Dev. 2009, 23: 912-927. 10.1101/gad.1782209.PubMed CentralView ArticlePubMedGoogle Scholar
- Lee KK, Starr D, Cohen M, Liu J, Han M, Wilson KL, Gruenbaum Y: Lamin-dependent localization of UNC-84, a protein required for nuclear migration in Caenorhabditis elegans. Mol Biol Cell. 2002, 13: 892-901. 10.1091/mbc.01-06-0294.PubMed CentralView ArticlePubMedGoogle Scholar
- Ding X, Xu R, Yu J, Xu T, Zhuang Y, Han M: SUN1 is required for telomere attachment to nuclear envelope and gametogenesis in mice. Dev Cell. 2007, 12: 863-872. 10.1016/j.devcel.2007.03.018.View ArticlePubMedGoogle Scholar
- Chi YH, Cheng LI, Myers T, Ward JM, Williams E, Su Q, Faucette L, Wang JY, Jeang KT: Requirement for Sun1 in the expression of meiotic reproductive genes and piRNA. Development. 2009, 136: 965-973. 10.1242/dev.029868.PubMed CentralView ArticlePubMedGoogle Scholar
- Lei K, Zhang X, Ding X, Guo X, Chen M, Zhu B, Xu T, Zhuang Y, Xu R, Han M: SUN1 and SUN2 play critical but partially redundant roles in anchoring nuclei in skeletal muscle cells in mice. Proc Natl Acad Sci USA. 2009, 106: 10207-10212. 10.1073/pnas.0812037106.PubMed CentralView ArticlePubMedGoogle Scholar
- Shultz LD, Lyons BL, Burzenski LM, Gott B, Samuels R, Schweitzer PA, Dreger C, Herrmann H, Kalscheuer V, Olins AL: Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly. Hum Mol Genet. 2003, 12: 61-69. 10.1093/hmg/ddg003.View ArticlePubMedGoogle Scholar
- Naetar N, Korbei B, Kozlov S, Kerenyi MA, Dorner D, Kral R, Gotic I, Fuchs P, Cohen TV, Bittner R: Loss of nucleoplasmic LAP2alpha-lamin A complexes causes erythroid and epidermal progenitor hyperproliferation. Nat Cell Biol. 2008, 10: 1341-1348. 10.1038/ncb1793.View ArticlePubMedGoogle Scholar
- Goldman RD, Shumaker DK, Erdos MR, Eriksson M, Goldman AE, Gordon LB, Gruenbaum Y, Khuon S, Mendez M, Varga R: Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci USA. 2004, 101: 8963-8968. 10.1073/pnas.0402943101.PubMed CentralView ArticlePubMedGoogle Scholar
- Capelson M, Hetzer MW: The role of nuclear pores in gene regulation, development and disease. EMBO Rep. 2009, 10: 697-705. 10.1038/embor.2009.147.PubMed CentralView ArticlePubMedGoogle Scholar
- Blower MD, Nachury M, Heald R, Weis K: A Rae1-containing ribonucleoprotein complex is required for mitotic spindle assembly. Cell. 2005, 121: 223-234. 10.1016/j.cell.2005.02.016.View ArticlePubMedGoogle Scholar
- Jeganathan KB, Malureanu L, van Deursen JM: The Rae1-Nup98 complex prevents aneuploidy by inhibiting securin degradation. Nature. 2005, 438: 1036-1039. 10.1038/nature04221.View ArticlePubMedGoogle Scholar
- Baker DJ, Jeganathan KB, Malureanu L, Perez-Terzic C, Terzic A, van Deursen JM: Early aging-associated phenotypes in Bub3/Rae1 haploinsufficient mice. J Cell Biol. 2006, 172: 529-540. 10.1083/jcb.200507081.PubMed CentralView ArticlePubMedGoogle Scholar
- Hardwick KG, Murray AW: Mad1p, a phosphoprotein component of the spindle assembly checkpoint in budding yeast. J Cell Biol. 1995, 131: 709-720. 10.1083/jcb.131.3.709.View ArticlePubMedGoogle Scholar
- Scott RJ, Lusk CP, Dilworth DJ, Aitchison JD, Wozniak RW: Interactions between Mad1p and the nuclear transport machinery in the yeast Saccharomyces cerevisiae. Mol Biol Cell. 2005, 16: 4362-4374. 10.1091/mbc.E05-01-0011.PubMed CentralView ArticlePubMedGoogle Scholar
- Chi YH, Haller K, Ward MD, Semmes OJ, Li Y, Jeang KT: Requirements for protein phosphorylation and the kinase activity of polo-like kinase 1 (Plk1) for the kinetochore function of mitotic arrest deficiency protein 1 (Mad1). J Biol Chem. 2008, 283: 35834-35844. 10.1074/jbc.M804967200.PubMed CentralView ArticlePubMedGoogle Scholar
- Iouk T, Kerscher O, Scott RJ, Basrai MA, Wozniak RW: The yeast nuclear pore complex functionally interacts with components of the spindle assembly checkpoint. J Cell Biol. 2002, 159: 807-819. 10.1083/jcb.200205068.PubMed CentralView ArticlePubMedGoogle Scholar
- Iwanaga Y, Chi YH, Miyazato A, Sheleg S, Haller K, Peloponese JM, Li Y, Ward JM, Benezra R, Jeang KT: Heterozygous deletion of mitotic arrest-deficient protein 1 (MAD1) increases the incidence of tumors in mice. Cancer Res. 2007, 67: 160-166. 10.1158/0008-5472.CAN-06-3326.View ArticlePubMedGoogle Scholar
- Michel LS, Liberal V, Chatterjee A, Kirchwegger R, Pasche B, Gerald W, Dobles M, Sorger PK, Murty VV, Benezra R: MAD2 haplo-insufficiency causes premature anaphase and chromosome instability in mammalian cells. Nature. 2001, 409: 355-359. 10.1038/35053094.View ArticlePubMedGoogle Scholar
- Chi YH, Ward JM, Cheng LI, Yasunaga J, Jeang KT: Spindle assembly checkpoint and p53 deficiencies cooperate for tumorigenesis in mice. Int J Cancer. 2009, 124: 1483-1489. 10.1002/ijc.24094.PubMed CentralView ArticlePubMedGoogle Scholar
- Chi YH, Jeang KT: Aneuploidy and cancer. J Cell Biochem. 2007, 102: 531-538. 10.1002/jcb.21484.View ArticlePubMedGoogle Scholar
- Boxus M, Twizere JC, Legros S, Dewulf JF, Kettmann R, Willems L: The HTLV-1 Tax interactome. Retrovirology. 2008, 5: 76-10.1186/1742-4690-5-76.PubMed CentralView ArticlePubMedGoogle Scholar
- Cremer T, Cremer M, Dietzel S, Muller S, Solovei I, Fakan S: Chromosome territories--a functional nuclear landscape. Curr Opin Cell Biol. 2006, 18: 307-316. 10.1016/j.ceb.2006.04.007.View ArticlePubMedGoogle Scholar
- Fraser P, Bickmore W: Nuclear organization of the genome and the potential for gene regulation. Nature. 2007, 447: 413-417. 10.1038/nature05916.View ArticlePubMedGoogle Scholar
- Spector DL: The dynamics of chromosome organization and gene regulation. Annu Rev Biochem. 2003, 72: 573-608. 10.1146/annurev.biochem.72.121801.161724.View ArticlePubMedGoogle Scholar
- Cabal GG, Genovesio A, Rodriguez-Navarro S, Zimmer C, Gadal O, Lesne A, Buc H, Feuerbach-Fournier F, Olivo-Marin JC, Hurt EC: SAGA interacting factors confine sub-diffusion of transcribed genes to the nuclear envelope. Nature. 2006, 441: 770-773. 10.1038/nature04752.View ArticlePubMedGoogle Scholar
- Taddei A, Van HG, Hediger F, Kalck V, Cubizolles F, Schober H, Gasser SM: Nuclear pore association confers optimal expression levels for an inducible yeast gene. Nature. 2006, 441: 774-778. 10.1038/nature04845.View ArticlePubMedGoogle Scholar
- Schmid M, Arib G, Laemmli C, Nishikawa J, Durussel T, Laemmli UK: Nup-PI: the nucleopore-promoter interaction of genes in yeast. Mol Cell. 2006, 21: 379-391. 10.1016/j.molcel.2005.12.012.View ArticlePubMedGoogle Scholar
- Pickersgill H, Kalverda B, de WE, Talhout W, Fornerod M, van SB: Characterization of the Drosophila melanogaster genome at the nuclear lamina. Nat Genet. 2006, 38: 1005-1014. 10.1038/ng1852.View ArticlePubMedGoogle Scholar
- Reddy KL, Zullo JM, Bertolino E, Singh H: Transcriptional repression mediated by repositioning of genes to the nuclear lamina. Nature. 2008, 452: 243-247. 10.1038/nature06727.View ArticlePubMedGoogle Scholar
- Somech R, Shaklai S, Geller O, Amariglio N, Simon AJ, Rechavi G, Gal-Yam EN: The nuclear-envelope protein and transcriptional repressor LAP2beta interacts with HDAC3 at the nuclear periphery, and induces histone H4 deacetylation. J Cell Sci. 2005, 118: 4017-4025. 10.1242/jcs.02521.View ArticlePubMedGoogle Scholar
- Shumaker DK, Dechat T, Kohlmaier A, Adam SA, Bozovsky MR, Erdos MR, Eriksson M, Goldman AE, Khuon S, Collins FS: Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging. Proc Natl Acad Sci USA. 2006, 103: 8703-8708. 10.1073/pnas.0602569103.PubMed CentralView ArticlePubMedGoogle Scholar
- Ding SL, Shen CY: Model of human aging: recent findings on Werner's and Hutchinson-Gilford progeria syndromes. Clin Interv Aging. 2008, 3: 431-444.PubMed CentralPubMedGoogle Scholar
- Hasty P, Campisi J, Hoeijmakers J, van SH, Vijg J: Aging and genome maintenance: lessons from the mouse?. Science. 2003, 299: 1355-1359. 10.1126/science.1079161.View ArticlePubMedGoogle Scholar
- Gonzalez-Suarez I, Redwood AB, Perkins SM, Vermolen B, Lichtensztejin D, Grotsky DA, Morgado-Palacin L, Gapud EJ, Sleckman BP, Sullivan T: Novel roles for A-type lamins in telomere biology and the DNA damage response pathway. EMBO J. 2009, 28: 2414-2427. 10.1038/emboj.2009.196.PubMed CentralView ArticlePubMedGoogle Scholar
- Liu B, Wang J, Chan KM, Tjia WM, Deng W, Guan X, Huang JD, Li KM, Chau PY, Chen DJ: Genomic instability in laminopathy-based premature aging. Nat Med. 2005, 11: 780-785. 10.1038/nm1266.View ArticlePubMedGoogle Scholar
- Kudlow BA, Stanfel MN, Burtner CR, Johnston ED, Kennedy BK: Suppression of proliferative defects associated with processing-defective lamin A mutants by hTERT or inactivation of p53. Mol Biol Cell. 2008, 19: 5238-5248. 10.1091/mbc.E08-05-0492.PubMed CentralView ArticlePubMedGoogle Scholar
- Dechat T, Gajewski A, Korbei B, Gerlich D, Daigle N, Haraguchi T, Furukawa K, Ellenberg J, Foisner R: LAP2alpha and BAF transiently localize to telomeres and specific regions on chromatin during nuclear assembly. J Cell Sci. 2004, 117: 6117-6128. 10.1242/jcs.01529.View ArticlePubMedGoogle Scholar
- Anderson DJ, Vargas JD, Hsiao JP, Hetzer MW: Recruitment of functionally distinct membrane proteins to chromatin mediates nuclear envelope formation in vivo. J Cell Biol. 2009, 186: 183-191. 10.1083/jcb.200901106.PubMed CentralView ArticlePubMedGoogle Scholar
- Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P: Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature. 2003, 423: 293-298. 10.1038/nature01629.View ArticlePubMedGoogle Scholar
- Chen L, Lee L, Kudlow BA, Dos Santos HG, Sletvold O, Shafeghati Y, Botha EG, Garg A, Hanson NB, Martin GM: LMNA mutations in atypical Werner's syndrome. Lancet. 2003, 362: 440-445. 10.1016/S0140-6736(03)14069-X.View ArticlePubMedGoogle Scholar
- Bonne G, Di Barletta MR, Varnous S, Becane HM, Hammouda EH, Merlini L, Muntoni F, Greenberg CR, Gary F, Urtizberea JA: Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat Genet. 1999, 21: 285-288. 10.1038/6799.View ArticlePubMedGoogle Scholar
- Raffaele Di BM, Ricci E, Galluzzi G, Tonali P, Mora M, Morandi L, Romorini A, Voit T, Orstavik KH, Merlini L: Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy. Am J Hum Genet. 2000, 66: 1407-1412. 10.1086/302869.View ArticleGoogle Scholar
- Muchir A, Bonne G, Kooi van der AJ, van MM, Baas F, Bolhuis PA, de VM, Schwartz K: Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B). Hum Mol Genet. 2000, 9: 1453-1459. 10.1093/hmg/9.9.1453.View ArticlePubMedGoogle Scholar
- Fatkin D, MacRae C, Sasaki T, Wolff MR, Porcu M, Frenneaux M, Atherton J, Vidaillet HJ, Spudich S, De GU: Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N Engl J Med. 1999, 341: 1715-1724. 10.1056/NEJM199912023412302.View ArticlePubMedGoogle Scholar
- De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL: Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse. Am J Hum Genet. 2002, 70: 726-736. 10.1086/339274.PubMed CentralView ArticlePubMedGoogle Scholar
- Cao H, Hegele RA: Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy. Hum Mol Genet. 2000, 9: 109-112. 10.1093/hmg/9.1.109.View ArticlePubMedGoogle Scholar
- Speckman RA, Garg A, Du F, Bennett L, Veile R, Arioglu E, Taylor SI, Lovett M, Bowcock AM: Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C. Am J Hum Genet. 2000, 66: 1192-1198. 10.1086/302836.PubMed CentralView ArticlePubMedGoogle Scholar
- Novelli G, Muchir A, Sangiuolo F, Helbling-Leclerc A, D'Apice MR, Massart C, Capon F, Sbraccia P, Federici M, Lauro R: Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C. Am J Hum Genet. 2002, 71: 426-431. 10.1086/341908.PubMed CentralView ArticlePubMedGoogle Scholar
- Navarro CL, Cadinanos J, De Sandre-Giovannoli A, Bernard R, Courrier S, Boccaccio I, Boyer A, Kleijer WJ, Wagner A, Giuliano F: Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors. Hum Mol Genet. 2005, 14: 1503-1513. 10.1093/hmg/ddi159.View ArticlePubMedGoogle Scholar
- Caux F, Dubosclard E, Lascols O, Buendia B, Chazouilleres O, Cohen A, Courvalin JC, Laroche L, Capeau J, Vigouroux C: A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathy. J Clin Endocrinol Metab. 2003, 88: 1006-1013. 10.1210/jc.2002-021506.View ArticlePubMedGoogle Scholar
- Bione S, Maestrini E, Rivella S, Mancini M, Regis S, Romeo G, Toniolo D: Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. Nat Genet. 1994, 8: 323-327. 10.1038/ng1294-323.View ArticlePubMedGoogle Scholar
- Fairley EA, Riddell A, Ellis JA, Kendrick-Jones J: The cell cycle dependent mislocalisation of emerin may contribute to the Emery-Dreifuss muscular dystrophy phenotype. J Cell Sci. 2002, 115: 341-354.PubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.