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Volumn 125, Issue 5, 2015, Pages 1796-1798

mRNA deadenylation and telomere disease

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MESSENGER RNA; POLYADENYLIC ACID SPECIFIC RIBONUCLEASE; PROTEIN P53; RIBONUCLEASE; UNCLASSIFIED DRUG; EXORIBONUCLEASE;

EID: 84929018125     PISSN: 00219738     EISSN: 15588238     Source Type: Journal    
DOI: 10.1172/JCI81506     Document Type: Note
Times cited : (9)

References (24)
  • 1
    • 0000605996 scopus 로고
    • Atrophia Cutis Reticularis cum Pigmentations, Dystrophia Unguium et Leukoplakis oris (Poikioodermia atrophicans vascularis Jacobi.)
    • Zinsser F. Atrophia Cutis Reticularis cum Pigmentations, Dystrophia Unguium et Leukoplakis oris (Poikioodermia atrophicans vascularis Jacobi.) Ikonographia Dermatologica. 1910;5:219-223.
    • (1910) Ikonographia Dermatologica , vol.5 , pp. 219-223
    • Zinsser, F.1
  • 3
    • 17344364484 scopus 로고    scopus 로고
    • 1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis
    • Knight SW, et al. 1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis. J Med Genet. 1998;35(12):993-996.
    • (1998) J Med Genet , vol.35 , Issue.12 , pp. 993-996
    • Knight, S.W.1
  • 4
    • 0031799895 scopus 로고    scopus 로고
    • X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions
    • Heiss NS, et al. X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions. Nat Genet. 1998;19(1):32-38.
    • (1998) Nat Genet , vol.19 , Issue.1 , pp. 32-38
    • Heiss, N.S.1
  • 6
    • 0031788801 scopus 로고    scopus 로고
    • Cbf5p, a potential pseudouridine synthase, and Nhp2p, a putative RNA-binding protein, are present together with Gar1p in all H BOX/ACA-motif snoRNPs and constitute a common bipartite structure
    • Watkins NJ, et al. Cbf5p, a potential pseudouridine synthase, and Nhp2p, a putative RNA-binding protein, are present together with Gar1p in all H BOX/ACA-motif snoRNPs and constitute a common bipartite structure. RNA. 1998;4(12):1549-1568.
    • (1998) RNA , vol.4 , Issue.12 , pp. 1549-1568
    • Watkins, N.J.1
  • 7
    • 0033518188 scopus 로고    scopus 로고
    • A telomerase component is defective in the human disease dyskeratosis congenita
    • Mitchell JR, Wood E, Collins K. A telomerase component is defective in the human disease dyskeratosis congenita. Nature. 1999;402(6761):551-555.
    • (1999) Nature , vol.402 , Issue.6761 , pp. 551-555
    • Mitchell, J.R.1    Wood, E.2    Collins, K.3
  • 8
    • 0035960043 scopus 로고    scopus 로고
    • The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
    • Vulliamy T, et al. The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature. 2001;413(6854):432-435.
    • (2001) Nature , vol.413 , Issue.6854 , pp. 432-435
    • Vulliamy, T.1
  • 9
    • 27644574342 scopus 로고    scopus 로고
    • Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita
    • Armanios M, et al. Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita. Proc Natl Acad Sci U S A. 2005;102(44):15960-15964.
    • (2005) Proc Natl Acad Sci U S A , vol.102 , Issue.44 , pp. 15960-15964
    • Armanios, M.1
  • 10
    • 18844421369 scopus 로고    scopus 로고
    • Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure
    • Vulliamy TJ, Walne A, Baskaradas A, Mason PJ, Marrone A, Dokal I. Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure. Blood Cells Mol Dis. 2005;34(3):257-263.
    • (2005) Blood Cells Mol Dis , vol.34 , Issue.3 , pp. 257-263
    • Vulliamy, T.J.1    Walne, A.2    Baskaradas, A.3    Mason, P.J.4    Marrone, A.5    Dokal, I.6
  • 11
    • 84888004712 scopus 로고    scopus 로고
    • Short telomeres: From dyskeratosis congenita to sporadic aplastic anemia and malignancy
    • Gramatges MM, Bertuch AA. Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy. Transl Res. 2013;162(6):353-363.
    • (2013) Transl Res , vol.162 , Issue.6 , pp. 353-363
    • Gramatges, M.M.1    Bertuch, A.A.2
  • 12
    • 84908642873 scopus 로고    scopus 로고
    • Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1
    • Guo Y, et al. Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1. Blood. 2014;124(18):2767-2774.
    • (2014) Blood , vol.124 , Issue.18 , pp. 2767-2774
    • Guo, Y.1
  • 13
    • 77954339095 scopus 로고    scopus 로고
    • Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study
    • Alter BP, et al. Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study. Br J Haematol. 2010;150(2):179-188.
    • (2010) Br J Haematol , vol.150 , Issue.2 , pp. 179-188
    • Alter, B.P.1
  • 14
    • 84928996799 scopus 로고    scopus 로고
    • Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita
    • Tummala H, et al. Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita. J Clin Invest. 2015;125(5):2151-2160.
    • (2015) J Clin Invest , vol.125 , Issue.5 , pp. 2151-2160
    • Tummala, H.1
  • 15
    • 17544385914 scopus 로고    scopus 로고
    • The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11→q13
    • Buiting K, Korner C, Ulrich B, Wahle E, Horsthemke B. The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11→q13. Cytogenet Cell Genet. 1999;87(1-2):125-131.
    • (1999) Cytogenet Cell Genet , vol.87 , Issue.1-2 , pp. 125-131
    • Buiting, K.1    Korner, C.2    Ulrich, B.3    Wahle, E.4    Horsthemke, B.5
  • 16
    • 77952584028 scopus 로고    scopus 로고
    • Nuclear deadenylation/polyadenylation factors regulate 3′ processing in response to DNA damage
    • Cevher MA, et al. Nuclear deadenylation/polyadenylation factors regulate 3′ processing in response to DNA damage. EMBO J. 2010;29(10):1674-1687.
    • (2010) EMBO J , vol.29 , Issue.10 , pp. 1674-1687
    • Cevher, M.A.1
  • 17
    • 84866149944 scopus 로고    scopus 로고
    • The PARN deadenylase targets a discrete set of mRNAs for decay and regulates cell motility in mouse myoblasts
    • Lee JE, Lee JY, Trembly J, Wilusz J, Tian B, Wilusz CJ. The PARN deadenylase targets a discrete set of mRNAs for decay and regulates cell motility in mouse myoblasts. PLoS Genet. 2012;8(8):e1002901.
    • (2012) PLoS Genet , vol.8 , Issue.8 , pp. e1002901
    • Lee, J.E.1    Lee, J.Y.2    Trembly, J.3    Wilusz, J.4    Tian, B.5    Wilusz, C.J.6
  • 18
    • 84874453925 scopus 로고    scopus 로고
    • Positive and negative feedback loops in the p53 and mRNA 3′ processing pathways
    • Devany E, Zhang X, Park JY, Tian B, Kleiman FE. Positive and negative feedback loops in the p53 and mRNA 3′ processing pathways. Proc Natl Acad Sci U S A. 2013;110(9):3351-3356.
    • (2013) Proc Natl Acad Sci U S A , vol.110 , Issue.9 , pp. 3351-3356
    • Devany, E.1    Zhang, X.2    Park, J.Y.3    Tian, B.4    Kleiman, F.E.5
  • 19
    • 84863625900 scopus 로고    scopus 로고
    • Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells
    • Ceccaldi R, et al. Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells. Cell Stem Cell. 2012;11(1):36-49.
    • (2012) Cell Stem Cell , vol.11 , Issue.1 , pp. 36-49
    • Ceccaldi, R.1
  • 20
    • 84863628325 scopus 로고    scopus 로고
    • Damage control and its costs: BM failure in Fanconi anemia stems from overactive p53/p21
    • Dumitriu B, Young NS. Damage control and its costs: BM failure in Fanconi anemia stems from overactive p53/p21. Cell Stem Cell. 2012;11(1):7-8.
    • (2012) Cell Stem Cell , vol.11 , Issue.1 , pp. 7-8
    • Dumitriu, B.1    Young, N.S.2
  • 21
    • 84865636769 scopus 로고    scopus 로고
    • Haploinsufficiency of ribosomal proteins and p53 activation in anemia: Diamond-Blackfan anemia and the 5q- syndrome
    • Boultwood J, Pellagatti A, Wainscoat JS. Haploinsufficiency of ribosomal proteins and p53 activation in anemia: Diamond-Blackfan anemia and the 5q- syndrome. Adv Biol Regul. 2012;52(1):196-203.
    • (2012) Adv Biol Regul , vol.52 , Issue.1 , pp. 196-203
    • Boultwood, J.1    Pellagatti, A.2    Wainscoat, J.S.3
  • 22
    • 0027530976 scopus 로고
    • p53 expression in dyskeratosis congenita: A marker for oral premalignancy?
    • Ogden GR, Lane DP, Chisholm DM. p53 expression in dyskeratosis congenita: a marker for oral premalignancy? J Clin Pathol. 1993;46(2):169-170.
    • (1993) J Clin Pathol , vol.46 , Issue.2 , pp. 169-170
    • Ogden, G.R.1    Lane, D.P.2    Chisholm, D.M.3
  • 23
    • 79951905790 scopus 로고    scopus 로고
    • The p53/p21(WAF/CIP) pathway mediates oxidative stress and senescence in dyskeratosis congenita cells with telomerase insufficiency
    • Westin ER, Aykin-Burns N, Buckingham EM, Spitz DR, Goldman FD, Klingelhutz AJ. The p53/p21(WAF/CIP) pathway mediates oxidative stress and senescence in dyskeratosis congenita cells with telomerase insufficiency. Antioxid Redox Signal. 2011;14(6):985-997.
    • (2011) Antioxid Redox Signal , vol.14 , Issue.6 , pp. 985-997
    • Westin, E.R.1    Aykin-Burns, N.2    Buckingham, E.M.3    Spitz, D.R.4    Goldman, F.D.5    Klingelhutz, A.J.6
  • 24
    • 84879794532 scopus 로고    scopus 로고
    • Mutant mice lacking the p53 C-terminal domain model telomere syndromes
    • Simeonova I, et al. Mutant mice lacking the p53 C-terminal domain model telomere syndromes. Cell Rep. 2013;3(6):2046-2058.
    • (2013) Cell Rep , vol.3 , Issue.6 , pp. 2046-2058
    • Simeonova, I.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.