1736
245474
ENSG00000130826
ENSMUSG00000031403
O60832
Q9ESX5
NM_001142463NM_001288747NM_001363
NM_001030307NM_001359411NM_001359412NM_001359413
NP_001135935NP_001275676NP_001354
NP_001025478NP_001346340NP_001346341NP_001346342
H/ACA ribonucleoprotein complex subunit 4 is a protein that in humans is encoded by the gene DKC1.[5][6][7]
Dyskerin is a pseudouridine synthase enzyme which is part of the TruB family of enzymes.[8] Dyskerin is an L-shaped protein of 514 residues and a molecular weight of about 58 kilo-daltons.[8] Dyskerin is essential for the activity of telomerase by accumulating telomerase RNA component (TERC).[8]
This gene is a member of the H/ACA snoRNPs (small nucleolar ribonucleoproteins) gene family. snoRNPs are involved in various aspects of rRNA processing and modification and have been classified into two families: C/D and H/ACA. The H/ACA snoRNPs also include the NOLA1, 2 and 3 proteins. The protein encoded by this gene and the three NOLA proteins localize to the dense fibrillar components of nucleoli and to coiled (Cajal) bodies in the nucleus. Both 18S rRNA production and rRNA pseudouridylation are impaired if any one of the four proteins is depleted. The protein encoded by this gene is related to the Saccharomyces cerevisiae Cbf5p and Drosophila melanogaster Nop60B proteins. The gene lies in a tail-to-tail orientation with the palmitoylated erythrocyte membrane protein (MPP1) gene and is transcribed in a telomere to centromere direction. Both nucleotide substitutions and single trinucleotide repeat polymorphisms have been found in this gene. Mutations in this gene cause X-linked dyskeratosis congenita.[7]
Mutations in DKC1 are associated to Hoyeraal-Hreidarsson syndrome.[9]
This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by expanding it.
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