Prelamin-A/C
Prelamin-A/C,orlamin A/Cis aproteinthat in humans is encoded by theLMNAgene.[5][6][7]Lamin A/C belongs to thelaminfamily of proteins.
Function
[edit]In the setting ofZMPSTE24deficiency, the final step of lamin processing does not occur, resulting in an accumulation of farnesyl-prelamin A. InHutchinson–Gilford progeria syndrome,a 50-amino acid deletion in prelamin A (amino acids 607–656) removes the site for the second endoproteolytic cleavage. Consequently, no mature lamin A is formed, and afarnesylatedmutant prelamin A (progerin) accumulates in cells.[9]Thenuclear laminaconsist of a two-dimensional matrix of proteins located next to theinner nuclear membrane.Thelaminfamily of proteins make up the matrix and are highly conserved in evolution. Duringmitosis,the lamina matrix is reversibly disassembled as the lamin proteins arephosphorylated.Lamin proteins are thought to be involved in nuclear stability,chromatinstructure and gene expression. Vertebrate lamins consist of two types, A and B. Throughalternate splicing,this gene encodes three type A lamin isoforms.[10]
Early in mitosis,maturation promoting factor(abbreviated MPF, also called mitosis-promoting factor or M-phase-promoting factor) phosphorylates specific serine residues in all three nuclear lamins, causing depolymerization of the lamin intermediate filaments. The phosphorylated lamin B dimers remain associated with the nuclear membrane via theirisoprenyl anchor.Lamin A is targeted to the nuclear membrane by an isoprenyl group but it is cleaved shortly after arriving at the membrane. It stays associated with the membrane through protein-protein interactions of itself and other membrane associated proteins, such asTOR1AIP1(LAP1). Depolymerization of the nuclear lamins leads to disintegration of the nuclear envelope.Transfectionexperiments demonstrate that phosphorylation of human lamin A is required for lamin depolymerization, and thus for disassembly of the nuclear envelope, which normally occurs early in mitosis.
Clinical significance
[edit]Mutations in theLMNAgene are associated with several diseases, includingEmery–Dreifuss muscular dystrophy,familial partial lipodystrophy,limb girdle muscular dystrophy,dilated cardiomyopathy,Charcot–Marie–Tooth disease,andrestrictive dermopathy.A truncated version of lamin A, commonly known asprogerin,causesHutchinson-Gilford-Progeria syndrome.[12][13]To date over 1,400SNPsare known[1].They can manifest in changes on mRNA, splicing or protein (e.g. Arg471Cys,[14] Arg482Gln,[15] Arg527Leu,[16]Arg527Cys,[17] Ala529Val[18] ) level.
DNA damage
[edit]DNA double-strand damagescan be repaired by eitherhomologous recombination(HR) ornon-homologous end joining(NHEJ). LMNA promotes genetic stability by maintaining the levels of proteins that have key roles in HR and NHEJ.[19][20]Mouse cells that are deficient for maturation of prelamin A have increased DNA damage and chromosome aberrations, and show increased sensitivity to DNA damaging agents.[21]Inprogeria,the inadequacy of DNA repair, due to defective LMNA, may cause features of premature aging (seeDNA damage theory of aging).
Interactions
[edit]LMNA has been shown tointeractwith:
References
[edit]- ^abcGRCh38: Ensembl release 89: ENSG00000160789–Ensembl,May 2017
- ^abcGRCm38: Ensembl release 89: ENSMUSG00000028063–Ensembl,May 2017
- ^"Human PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^"Mouse PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^Lin F, Worman HJ (1993)."Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C".J Biol Chem.268(22): 16321–16326.doi:10.1016/S0021-9258(19)85424-8.PMID8344919.
- ^Kamat AK, Rocchi M, Smith DI, Miller OJ (March 1993). "Lamin A/C gene and a related sequence map to human chromosomes 1q12.1-q23 and 10".Somat. Cell Mol. Genet.19(2): 203–8.doi:10.1007/BF01233534.PMID8511676.S2CID32913788.
- ^Wydner KL, McNeil JA, Lin F, Worman HJ, Lawrence JB (March 1996)."Chromosomal assignment of human nuclear envelope protein genes LMNA, LMNB1, and LBR by fluorescence in situ hybridization".Genomics.32(3): 474–8.doi:10.1006/geno.1996.0146.PMID8838815.
- ^Buxboim A, Swift J, Irianto J, Spinler KR, Dingal PC, Athirasala A, Kao YR, Cho S, Harada T, Shin JW, Discher DE (2014)."Matrix elasticity regulates lamin-A,C phosphorylation and turnover with feedback to actomyosin".Current Biology.24(16): 1909–17.Bibcode:2014CBio...24.1909B.doi:10.1016/j.cub.2014.07.001.PMC4373646.PMID25127216.
- ^Coutinho HD, Falcão-Silva VS, Gonçalves GF, da Nóbrega RB (2009)."Molecular ageing in progeroid syndromes: Hutchinson–Gilford progeria syndrome as a model".Immun Ageing.6:4.doi:10.1186/1742-4933-6-4.PMC2674425.PMID19379495.
- ^"Entrez Gene: LMNA lamin A/C".
- ^Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, Shams A, Ahmad N, Hamed S, Puzianowska-Kuznicka M (2012)."A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome".Eur J Hum Genet.20(11): 1134–40.doi:10.1038/ejhg.2012.77.PMC3476705.PMID22549407.
- ^Capell BC, Collins FS (December 2006). "Human laminopathies: nuclei gone genetically awry".Nat. Rev. Genet.7(12): 940–52.doi:10.1038/nrg1906.PMID17139325.S2CID13438737.
- ^Rankin J, Ellard S (October 2006). "The laminopathies: a clinical review".Clin. Genet.70(4): 261–74.doi:10.1111/j.1399-0004.2006.00677.x.PMID16965317.S2CID7234475.
- ^Zirn B, Kress W, Grimm T, Berthold LD, Neubauer B, Kuchelmeister K, Müller U, Hahn A (2008). "Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy".Am J Med Genet A.146A(8): 1049–1054.doi:10.1002/ajmg.a.32259.PMID18348272.S2CID205309256.
- ^Cao H, Hegele RA (2002)."Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy".Hum. Mol. Genet.9(1): 109–12.doi:10.1093/hmg/9.1.109.PMID10587585.
- ^Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, Shams A, Ahmad N, Hamed S, Puzianowska-Kuznicka M (2012)."A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome".Eur J Hum Genet.20(11): 1134–40.doi:10.1038/ejhg.2012.77.PMC3476705.PMID22549407.
- ^Agarwal AK, Kazachkova I, Ten S, Garg A (2008)."Severe mandibuloacral dysplasia-associated lipodystrophy and progeria in a young girl with a novel homozygous Arg527Cys LMNA mutation".J Clin Endocrinol Metab.93(12): 4617–4623.doi:10.1210/jc.2008-0123.PMC2626450.PMID18796515.
- ^Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK (2005)."A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia".J. Clin. Endocrinol. Metab.90(9): 5259–64.doi:10.1210/jc.2004-2560.PMID15998779.
- ^Redwood AB, Perkins SM, Vanderwaal RP, Feng Z, Biehl KJ, Gonzalez-Suarez I, Morgado-Palacin L, Shi W, Sage J, Roti-Roti JL, Stewart CL, Zhang J, Gonzalo S (2011)."A dual role for A-type lamins in DNA double-strand break repair".Cell Cycle.10(15): 2549–60.doi:10.4161/cc.10.15.16531.PMC3180193.PMID21701264.
- ^Gonzalo S, Kreienkamp R (2015)."DNA repair defects and genome instability in Hutchinson-Gilford Progeria Syndrome".Curr. Opin. Cell Biol.34:75–83.doi:10.1016/j.ceb.2015.05.007.PMC4522337.PMID26079711.
- ^Liu B, Wang J, Chan KM, Tjia WM, Deng W, Guan X, Huang JD, Li KM, Chau PY, Chen DJ, Pei D, Pendas AM, Cadiñanos J, López-Otín C, Tse HF, Hutchison C, Chen J, Cao Y, Cheah KS, Tryggvason K, Zhou Z (2005). "Genomic instability in laminopathy-based premature aging".Nat. Med.11(7): 780–5.doi:10.1038/nm1266.PMID15980864.S2CID11798376.
- ^Tang K, Finley RL, Nie D, Honn KV (March 2000). "Identification of 12-lipoxygenase interaction with cellular proteins by yeast two-hybrid screening".Biochemistry.39(12): 3185–91.doi:10.1021/bi992664v.PMID10727209.
- ^Wilkinson FL, Holaska JM, Zhang Z, Sharma A, Manilal S, Holt I, Stamm S, Wilson KL, Morris GE (June 2003)."Emerin interacts in vitro with the splicing-associated factor, YT521-B".Eur. J. Biochem.270(11): 2459–66.doi:10.1046/j.1432-1033.2003.03617.x.PMID12755701.S2CID5963743.
- ^Lattanzi G, Cenni V, Marmiroli S, Capanni C, Mattioli E, Merlini L, Squarzoni S, Maraldi NM (April 2003). "Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts".Biochem. Biophys. Res. Commun.303(3): 764–70.doi:10.1016/S0006-291X(03)00415-7.PMID12670476.
- ^Sakaki M, Koike H, Takahashi N, Sasagawa N, Tomioka S, Arahata K, Ishiura S (February 2001). "Interaction between emerin and nuclear lamins".J. Biochem.129(2): 321–7.doi:10.1093/oxfordjournals.jbchem.a002860.PMID11173535.
- ^Clements L, Manilal S, Love DR, Morris GE (January 2000). "Direct interaction between emerin and lamin A".Biochem. Biophys. Res. Commun.267(3): 709–14.doi:10.1006/bbrc.1999.2023.PMID10673356.
- ^Barton RM, Worman HJ (October 1999)."Prenylated prelamin A interacts with Narf, a novel nuclear protein".J. Biol. Chem.274(42): 30008–18.doi:10.1074/jbc.274.42.30008.PMID10514485.
- ^Lloyd DJ, Trembath RC, Shackleton S (April 2002)."A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies".Hum. Mol. Genet.11(7): 769–77.doi:10.1093/hmg/11.7.769.PMID11929849.
- ^Markiewicz E, Dechat T, Foisner R, Quinlan RA, Hutchison CJ (December 2002)."Lamin A/C binding protein LAP2 Alpha is required for nuclear anchorage of retinoblastoma protein".Mol. Biol. Cell.13(12): 4401–13.doi:10.1091/mbc.E02-07-0450.PMC138642.PMID12475961.
- ^Dechat T, Korbei B, Vaughan OA, Vlcek S, Hutchison CJ, Foisner R (October 2000). "Lamina-associated polypeptide 2 Alpha binds intranuclear A-type lamins".J. Cell Sci.113(19): 3473–84.doi:10.1242/jcs.113.19.3473.PMID10984438.
- ^Dreuillet C, Tillit J, Kress M, Ernoult-Lange M (November 2002)."In vivo and in vitro interaction between human transcription factor MOK2 and nuclear lamin A/C".Nucleic Acids Res.30(21): 4634–42.doi:10.1093/nar/gkf587.PMC135794.PMID12409453.
- ^Liu B, Ghosh S, Yang X, Zheng H, Liu X, Wang Z, Jin G, Zheng B, Kennedy BK, Suh Y, Kaeberlein M, Tryggvason K, Zhou Z (2012)."Resveratrol Rescues SIRT1-Dependent Adult Stem Cell Decline and Alleviates Progeroid Features in Laminopathy-Based Progeria".Cell Metabolism.16(6): 738–750.doi:10.1016/j.cmet.2012.11.007.PMID23217256.
Further reading
[edit]- Gruenbaum Y, Wilson KL, Harel A, Goldberg M, Cohen M (2000). "Review: nuclear lamins--structural proteins with fundamental functions".J. Struct. Biol.129(2–3): 313–23.doi:10.1006/jsbi.2000.4216.PMID10806082.
- Worman HJ, Courvalin JC (2000). "The inner nuclear membrane".J. Membr. Biol.177(1): 1–11.doi:10.1007/s002320001096.PMID10960149.S2CID20121844.
- Burke B, Mounkes LC, Stewart CL (2002)."The nuclear envelope in muscular dystrophy and cardiovascular diseases".Traffic.2(10): 675–83.doi:10.1034/j.1600-0854.2001.21001.x.PMID11576443.S2CID19392394.
- Mounkes LC, Burke B, Stewart CL (2001). "The A-type lamins: nuclear structural proteins as a focus for muscular dystrophy and cardiovascular diseases".Trends Cardiovasc. Med.11(7): 280–5.doi:10.1016/S1050-1738(01)00126-8.PMID11709282.
- Vigouroux C, Magré J, Desbois-Mouthon C, Lascols O, Cherqui G, Caron M, Capeau J (2002). "[Major insulin resistance syndromes: clinical and physiopathological aspects]".J. Soc. Biol.195(3): 249–57.doi:10.1051/jbio/2001195030249.PMID11833462.S2CID70531120.
- Helbling-Leclerc A, Bonne G, Schwartz K (2002)."Emery–Dreifuss muscular dystrophy".Eur. J. Hum. Genet.10(3): 157–61.doi:10.1038/sj.ejhg.5200744.PMID11973618.
- Burke B, Stewart CL (2002). "Life at the edge: the nuclear envelope and human disease".Nat. Rev. Mol. Cell Biol.3(8): 575–85.doi:10.1038/nrm879.PMID12154369.S2CID11913118.
- Novelli G, D'Apice MR (2004). "The strange case of the" lumper "lamin A/C gene and human premature ageing".Trends in Molecular Medicine.9(9): 370–5.doi:10.1016/S1471-4914(03)00162-X.PMID13129702.
- Pasotti M, Repetto A, Pisani A, Arbustini E (2004). "[Diseases associated with lamin A/C gene defects: what the clinical cardiologist ought to know]".Italian Heart Journal Supplement.5(2): 98–111.PMID15080529.
- Al-Shali KZ, Hegele RA (2005)."Laminopathies and atherosclerosis".Arterioscler. Thromb. Vasc. Biol.24(9): 1591–5.doi:10.1161/01.ATV.0000136392.59656.8b.PMID15205220.
- Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK (2005)."A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia".J. Clin. Endocrinol. Metab.90(9): 5259–64.doi:10.1210/jc.2004-2560.PMID15998779.
- Lees-Miller SP (2006). "Dysfunction of lamin A triggers a DNA damage response and cellular senescence".DNA Repair (Amst.).5(2): 286–9.doi:10.1016/j.dnarep.2005.10.007.PMID16344005.
- Donadille B, Lascols O, Capeau J, Vigouroux C (2006). "Etiological investigations in apparent type 2 diabetes: when to search for lamin A/C mutations?".Diabetes Metab.31(6): 527–32.doi:10.1016/S1262-3636(07)70227-6.PMID16357800.
- Young SG, Meta M, Yang SH, Fong LG (2007)."Prelamin A farnesylation and progeroid syndromes".J. Biol. Chem.281(52): 39741–5.doi:10.1074/jbc.R600033200.PMID17090536.
- Halaschek-Wiener J, Brooks-Wilson A (2007)."Progeria of stem cells: stem cell exhaustion in Hutchinson–Gilford progeria syndrome"(PDF).J. Gerontol. A Biol. Sci. Med. Sci.62(1): 3–8.doi:10.1093/gerona/62.1.3.PMID17301031.Archived fromthe original(PDF)on 2012-11-05.Retrieved2019-08-15.
- Mazereeuw-Hautier J, Wilson LC, Mohammed S, Smallwood D, Shackleton S, Atherton DJ, Harper JI (2007). "Hutchinson–Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature".Br. J. Dermatol.156(6): 1308–14.doi:10.1111/j.1365-2133.2007.07897.x.PMID17459035.S2CID25944330.
- Sliwińska MA (2007). "[The role of lamins and mutations of LMNA gene in physiological and premature aging] Polish".Postepy Biochem.53(1): 46–52.PMID17718387.
- Genschel J, Schmidt HH (December 2000). "Mutations in the LMNA gene encoding lamin A/C".Hum. Mutat.16(6): 451–9.doi:10.1002/1098-1004(200012)16:6<451::AID-HUMU1>3.0.CO;2-9.PMID11102973.S2CID19320913.
- Scaffidi P, Misteli T (April 2005)."Reversal of the cellular phenotype in the premature aging disease Hutchinson–Gilford progeria syndrome".Nat. Med.11(4): 440–5.doi:10.1038/nm1204.PMC1351119.PMID15750600.
- Bird TD, Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A (1993). "Charcot–Marie–Tooth Neuropathy Type 2".PMID20301462.
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(help) - Sparks SE, Quijano-Roy S, Harper A, Rutkowski A, Gordon E, Hoffman EP, Pegoraro E, Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A (1993). "Congenital Muscular Dystrophy Overview".PMID20301468.
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(help) - Hershberger RE, Morales A, Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A (1993). "LMNA-Related Dilated Cardiomyopathy ".PMID20301717.
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(help) - Pegoraro E, Hoffman EP, Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A (1993). "Limb-Girdle Muscular Dystrophy Overview".PMID20301582.
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(help) - Bonne G, Leturcq F, Ben Yaou R, Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A (1993). "Emery–Dreifuss Muscular Dystrophy".PMID20301609.
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(help) - Gordon LB, Brown WT, Collins FS, Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A (1993). "Hutchinson–Gilford Progeria Syndrome".PMID20301300.
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(help) - Martín B, Smith RJH, Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A (1993). "Dense Deposit Disease/Membranoproliferative Glomerulonephritis Type II".PMID20301598.
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External links
[edit]- Online Mendelian Inheritance in Man(OMIM):Cardiomyopathy, Dilated, 1A; CMD1A - 115200
- Online Mendelian Inheritance in Man(OMIM):LAMIN A/C; LMNA - 150330
- LMNA+protein,+humanat the U.S. National Library of MedicineMedical Subject Headings(MeSH)
- LOVDmutation database:LMNA
- GeneCards for LMNA
- Laminopathy Information Site for Lay Public