Dyskeratosis congenita: Difference between revisions

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====X-linked form====
====X-linked form====
The best characterized form of dyskeratosis congenita is a result of one or more mutations in the long arm of the [[X chromosome]] in the gene DKC1.<ref name="pmid11574891" /><ref name="pmid9590285" /> This results in the X-linked recessive form of the disease wherein the major protein affected is dyskerin. Of the five mutations described by Heiss and colleagues in ''Nature Genetics'',<ref name="pmid9590285" /> four were single nucleotide polymorphisms all resulting in the change of highly [[Conserved sequence|conserved amino acids]]. One case was an in-frame deletion resulting in the loss of a [[leucine]] [[amino acid|residue]], also conserved in mammals. In three of the cases, the specific amino acids affected ([[phenylalanine]], [[proline]], [[glycine]]) are found in the same [[locus (genetics)|locus]] in humans as they are in yeast (''[[S. Cerevisiae]]'') and the [[brown rat]] (''R. Norvegicus'').<ref name="pmid9590285" /> This establishes the sequence conservation and importance of dyskerin within the eukaryotes. The relevant nature of dyskerin throughout most species is to catalyze the [[RNA transcription|post-transcriptional]] [[pseudouridine|pseudouridylation]] of specific [[uridine]]s found in non-coding RNAs, such as [[ribosomal RNA]] (rRNA). Cbf5, the yeast analog of human dyskerin, is indeed known to be associated with the processing and maturation of rRNA.<ref name="pmid11574891" /> In humans this role can be attributed to dyskerin.<ref name="pmid9590285" /> Thus, the X-linked form of this disease may result in specific issues related to dysfunctional rRNA and perhaps a graver phenotype. Within the vertebrates, as opposed to single celled eukaryotes, dyskerin is a key component of the telomerase RNA component (TERC) in the form of the H/ACA motif.<ref name="pmid17015423" /> This X-linked variety, like the Nop10 and Nhp2 mutations, demonstrates shortened telomeres as a result of lower TERC concentrations.
The best characterized form of dyskeratosis congenita is a result of one or more mutations in the long arm of the [[X chromosome]] in the gene DKC1.<ref name="pmid11574891" /><ref name="pmid9590285" /> This results in the X-linked recessive form of the disease wherein the major protein affected is dyskerin. Of the five mutations described by Heiss and colleagues in ''Nature Genetics'',<ref name="pmid9590285" /> four were single nucleotide polymorphisms all resulting in the change of highly [[Conserved sequence|conserved amino acids]]. One case was an in-frame deletion resulting in the loss of a [[leucine]] [[amino acid|residue]], also conserved in mammals. In three of the cases, the specific amino acids affected ([[phenylalanine]], [[proline]], [[glycine]]) are found in the same [[locus (genetics)|locus]] in humans as they are in yeast (''[[S. Cerevisiae]]'') and the [[brown rat]] (''R. Norvegicus'').<ref name="pmid9590285" /> This establishes the sequence conservation and importance of dyskerin within the eukaryotes. The relevant nature of dyskerin throughout most species is to catalyze the [[RNA transcription|post-transcriptional]] [[pseudouridine|pseudouridylation]] of specific [[uridine]]s found in non-coding RNAs, such as [[ribosomal RNA]] (rRNA). Cbf5, the yeast analog of human dyskerin, is indeed known to be associated with the processing and maturation of rRNA.<ref name="pmid11574891" /> In humans this role can be attributed to dyskerin.<ref name="pmid9590285" /> Thus, the X-linked form of this disease may result in specific issues related to dysfunctional rRNA and perhaps a graver phenotype. Within the vertebrates, as opposed to single celled eukaryotes, dyskerin is a key component of the telomerase RNA component (TERC) in the form of the H/ACA motif.<ref name="pmid17015423" /> This X-linked variety, like the Nop10 and Nhp2 mutations, demonstrates shortened telomeres as a result of lower TERC concentrations.
====Autosomal dominant form====
The evidence supporting the importance of the H/ACA domain in human telomerase is abundant. At least one study<ref name="pmid19095616">{{cite journal |author=Trahan C, Dragon F |title=Dyskeratosis congenita mutations in the H/ACA domain of human telomerase RNA affect its assembly into a pre-RNP. |journal=RNA |volume=15 |issue=2 |pages=235–43 |year=2009 |month=February|pmid=19095616|url=http://rnajournal.cshlp.org/content/15/2/235.long |doi=10.1261/rna.1354009 |pmc=2648702}}</ref> has shown that these mutations affect telomerase activity by negatively affecting pre-RNP assembly and maturation of human telomerase RNA. Nonetheless, mutations which directly affect the telomerase RNA components would presumably exist and should also cause premature aging or DKC-like symptoms. Indeed, three families with mutations in the human TERC gene have been studied with intriguing results.<ref name="pmid11574891" /> In two of these families, two family-specific single nucleotide polymorphisms were present while in the other there persisted a large-scale deletion (821 base pairs of DNA) on [[Chromosome 3 (human)|chromosome 3]] which includes 74 bases coding for a section of the H/ACA domain. These three different mutations result in a mild form of dyskeratosis congenita which uniquely follows an autosomal dominant pattern of inheritance. Premature graying, early dental loss, predisposition to skin cancer, as well as shortening of telomere length continue to be characteristic of this disease.

Revision as of 15:51, 24 July 2012

Dyskeratosis congenita
ICD-10 Q82.8
ICD-9 757.39
OMIM 305000
DiseasesDB 30105
eMedicine derm/111 
MeSH D019871

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]

Overview

Dyskeratosis congenita (DKC), also called Zinsser-Cole-Engman syndrome,[1][2]:570 is a rare progressive congenital disorder that in some ways resembles premature aging (similar to progeria). The disease mainly affects the integumentary system, the organ system that protects the body from damage, with a major consequence being anomalies of the bone marrow.

Pathophysiology

Though the exact pathology of the disease is not yet fully understood, most evidence points to dyskeratosis congenita being primarily a disorder of poor telomere maintenance.[3] Specifically, the disease is related to one or more mutations which directly or indirectly affect the vertebrate telomerase RNA component (TERC).

Telomerase is a reverse transcriptase which maintains a specific repeat sequence of DNA, the telomere, during development. Telomeres are placed by telomerase on both ends of linear chromosomes as a way to protect linear DNA from general forms of chemical damage and to correct for the chromosomal end-shortening that occurs during normal DNA replication.[4] This end-shortening is the result of the eukaryotic DNA polymerases having no mechanism for synthesizing the final nucleotides present on the end of the "lagging strand" of double stranded DNA. DNA polymerase can only synthesize new DNA from an old DNA strand in the 5'->3' direction. Given that DNA has two strands that are complementary, one strand must be 5'->3' while the other is 3'->5'. This inability to synthesize in the 3'->5' directionality is compensated with the use of Okazaki fragments, short pieces of DNA that are synthesized 5'->3' from the 3'->5' as the replication fork moves. As DNA polymerase requires RNA primers for DNA binding in order to commence replication, each Okazaki fragment is thus preceded by an RNA primer on the strand being synthesized. When the end of the chromosome is reached, the final RNA primer is placed upon this nucleotide region, and it is inevitably removed. Unfortunately once the primer is removed, DNA polymerase is unable to synthesize the remaining bases.[4][5]

Sufferers of DKC have been shown to have a reduction in TERC levels invariably affecting the normal function of telomerase which maintains these telomeres.[3][6][7] With TERC levels down, telomere maintenance during development suffers accordingly. In humans, telomerase is inactive in most cell types after early development (except in extreme cases such as cancer).[8] Thus, if telomerase is not able to efficiently affect the DNA in the beginning of life, chromosomal instability becomes a grave possibility in individuals much earlier than would be expected.[citation needed]

A study shows that proliferative defects in DC skin keratinocytes are corrected by expression of the telomerase reverse transcriptase, TERT, or by activation of endogenous telomerase through expression of papillomavirus E6/E7 or the telomerase RNA component, TERC. Experimental Dermatology 2010; 19: 279–288[9]

Genetics

Of the components of the telomerase RNA component (TERC), one of key importance is the box H/ACA domain. This H/ACA domain is responsible for maturation and stability of TERC and therefore of telomerase as a whole. The mammalian H/ACA ribonucleoprotein contains four protein subunits: dyskerin, Gar1, Nop10, and Nhp2. Mutations in Nop10,[6] Nhp2[10] and dyskerin1[7] have all been shown to lead to DKC-like symptoms.


Autosomal recessive form

The true phenotype of DKC individuals may depend upon which protein has incurred a mutation. One documented autosomal recessive mutation[6] in a family that carries DKC has been found in Nop10. Specifically, the mutation is a change of base from cytosine to thymine in a highly conserved region of the Nop10 sequence. This mutation, on chromosome 15, results in an amino acid change from arginine to tryptophan. Homozygous recessive individuals show the symptoms of dyskeratosis congenita in full. As compared to age-matched normal individuals, those suffering from DKC have telomeres of a much shorter length. Furthermore, heterozygotes, those who have one normal allele and one coding for the disease, also show relatively shortened telomeres. The cause of this was determined to be a reduction in TERC levels in those with the Nop10 mutation. With TERC levels down, telomere maintenance, especially in development, would be presumed to suffer accordingly. This would lead to the telomere shortening described.[6]

Nhp2 mutations are similar in characterization to Nop10. These mutations are also autosomal recessive with three specific single-nucleotide polymorphisms being recognized which result in dyskeratosis congenita. Also like Nop10, individuals with these Nhp2 mutations have a reduction in the amount of telomerase RNA component (TERC) present in the cell. Again it can be presumed that a reduction in TERC results in aberrant telomere maintenance and thus shortened telomeres. Those homozygous recessive for mutations in Nhp2 do show shorter telomeres when compared with age-matched normal individuals.[10]

X-linked form

The best characterized form of dyskeratosis congenita is a result of one or more mutations in the long arm of the X chromosome in the gene DKC1.[3][7] This results in the X-linked recessive form of the disease wherein the major protein affected is dyskerin. Of the five mutations described by Heiss and colleagues in Nature Genetics,[7] four were single nucleotide polymorphisms all resulting in the change of highly conserved amino acids. One case was an in-frame deletion resulting in the loss of a leucine residue, also conserved in mammals. In three of the cases, the specific amino acids affected (phenylalanine, proline, glycine) are found in the same locus in humans as they are in yeast (S. Cerevisiae) and the brown rat (R. Norvegicus).[7] This establishes the sequence conservation and importance of dyskerin within the eukaryotes. The relevant nature of dyskerin throughout most species is to catalyze the post-transcriptional pseudouridylation of specific uridines found in non-coding RNAs, such as ribosomal RNA (rRNA). Cbf5, the yeast analog of human dyskerin, is indeed known to be associated with the processing and maturation of rRNA.[3] In humans this role can be attributed to dyskerin.[7] Thus, the X-linked form of this disease may result in specific issues related to dysfunctional rRNA and perhaps a graver phenotype. Within the vertebrates, as opposed to single celled eukaryotes, dyskerin is a key component of the telomerase RNA component (TERC) in the form of the H/ACA motif.[8] This X-linked variety, like the Nop10 and Nhp2 mutations, demonstrates shortened telomeres as a result of lower TERC concentrations.


Autosomal dominant form

The evidence supporting the importance of the H/ACA domain in human telomerase is abundant. At least one study[11] has shown that these mutations affect telomerase activity by negatively affecting pre-RNP assembly and maturation of human telomerase RNA. Nonetheless, mutations which directly affect the telomerase RNA components would presumably exist and should also cause premature aging or DKC-like symptoms. Indeed, three families with mutations in the human TERC gene have been studied with intriguing results.[3] In two of these families, two family-specific single nucleotide polymorphisms were present while in the other there persisted a large-scale deletion (821 base pairs of DNA) on chromosome 3 which includes 74 bases coding for a section of the H/ACA domain. These three different mutations result in a mild form of dyskeratosis congenita which uniquely follows an autosomal dominant pattern of inheritance. Premature graying, early dental loss, predisposition to skin cancer, as well as shortening of telomere length continue to be characteristic of this disease.

  1. ↑ Online Mendelian Inheritance in Man (OMIM) 305000
  2. ↑ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
  3. ↑ 3.0 3.1 3.2 3.3 3.4 Vulliamy T, Marrone A, Goldman F; et al. (2001). "The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita". Nature. 413 (6854): 432–435. doi:10.1038/35096585. PMID 11574891. Unknown parameter |month= ignored (help)
  4. ↑ 4.0 4.1 Greider, CW. (1996). "Telomere length regulation". Annu. Rev. Biochem. 65: 337–365. doi:10.1146/annurev.bi.65.070196.002005?url_ver=Z39.88-2003. PMID 8811183. Unknown parameter |month= ignored (help)
  5. ↑ Wason, James; et al. (2004). Molecular Biology of the Gene. 5th ed. Annu. Rev. Biochem. San Francisco: Pearson Education, Inc.
  6. ↑ 6.0 6.1 6.2 6.3 Walne AJ, Vulliamy T, Marrone A; et al. (2007). "Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10". Hum Mol Genet. 16 (13): 1619–29. doi:10.1093/hmg/ddm111. PMC 2882227. PMID 17507419. Unknown parameter |month= ignored (help)
  7. ↑ 7.0 7.1 7.2 7.3 7.4 7.5 Heiss NS, Knight SW, Vulliamy TJ; et al. (1998). "X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions". Nat. Genet. 19 (1): 32–38. doi:10.1038/ng0598-32. PMID 9590285. Unknown parameter |month= ignored (help)
  8. ↑ 8.0 8.1 Wong J, Collins K (2006). "Telomerase RNA level limits telomere maintenance in X-linked dyskeratosis congenita". Genes Dev. 20 (20): 2848–2858. doi:10.1101/gad.1476206. PMC 1619937. PMID 17015423. Unknown parameter |month= ignored (help)
  9. ↑ Gourronc, F. A., Robertson, M. M., Herrig, A. K., Lansdorp, P. M., Goldman, F. D. and Klingelhutz, A. J. (2010), Proliferative defects in dyskeratosis congenita skin keratinocytes are corrected by expression of the telomerase reverse transcriptase, TERT, or by activation of endogenous telomerase through expression of papillomavirus E6/E7 or the telomerase RNA component, TERC. Experimental Dermatology, 19: 279–288. doi:10.1111/j.1600-0625.2009.00916.x
  10. ↑ 10.0 10.1 Vulliamy T, Beswick R, Kirwan M; et al. (2008). "Mutations in the telomerase component Nhp2 cause the premature ageing syndrome dyskeratosis congenita". Proc Natl Acad Sci USA. 105 (23): 8073–8. doi:10.1073/pnas.0800042105. PMC 2430361. PMID 18523010. Unknown parameter |month= ignored (help)
  11. ↑ Trahan C, Dragon F (2009). "Dyskeratosis congenita mutations in the H/ACA domain of human telomerase RNA affect its assembly into a pre-RNP". RNA. 15 (2): 235–43. doi:10.1261/rna.1354009. PMC 2648702. PMID 19095616. Unknown parameter |month= ignored (help)
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