RECQL4

From Wikipedia, the free encyclopedia

RecQ protein-like 4

Identifiers

RECQL4; RTS; RECQ4

External IDs

OMIM: 603780 MGI: 1931028 HomoloGene: 3144

Gene ontology
Molecular Function:	• nucleotide binding • nucleic acid binding • DNA helicase activity • ATP binding • ATP-dependent helicase activity • zinc ion binding • hydrolase activity
Cellular Component:	• nucleus
Biological Process:	• DNA repair • DNA recombination • multicellular organismal development

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

Refseq

NM_004260 (mRNA)
NP_004251 (protein)

XM_903254 (mRNA)
XP_908347 (protein)

Location

Chr 8: 145.71 - 145.71 Mb

Chr 15: 76.53 - 76.54 Mb

Pubmed search

[1]

[2]

RecQ protein-like 4, also known as RECQL4, is a human gene.^[1]

Mutations in RECQL4 are associated with the autosomal recessive disease Rothmund-Thomson Syndrome. There are two types of Rothmund Thomson syndrome and it is Type 2 that is caused by patients carrying deleterious mutations in both copies of the RECQL4 gene. This condition is associated with a high risk of developing osteosarcoma (malignant tumor of the bone).^[2] RECQL4 gets it name from being homologous (sharing sequence) with other members of the RecQ helicase family. Two other genetic diseases are due to mutations in other RECQ helicases. Bloom syndrome is associated with mutations in the BLM gene and Werner syndrome is associated with mutations in the WRN gene.^[3]

[edit] References

^ Entrez Gene: RECQL4 RecQ protein-like 4.
^ Wang LL, Gannavarapu A, Kozinetz CA, et al. (2003). "Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome.". J. Natl. Cancer Inst. 95 (9): 669-74. PMID 12734318.
^ Kitao S, Lindor NM, Shiratori M, et al. (2000). "Rothmund-thomson syndrome responsible gene, RECQL4: genomic structure and products.". Genomics 61 (3): 268-76. doi:10.1006/geno.1999.5959. PMID 10552928.

[edit] Further reading

Kellermayer R (2006). "The versatile RECQL4.". Genet. Med. 8 (4): 213-6. doi:10.1097/01.gim.0000214457.58378.1a. PMID 16617241.
Soukup T (1976). "Intrafusal fibre types in rat limb muscle spindles: morphological and histochemical characteristics.". Histochemistry 47 (1): 43-57. PMID 133085.
Kitao S, Ohsugi I, Ichikawa K, et al. (1999). "Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes.". Genomics 54 (3): 443-52. doi:10.1006/geno.1998.5595. PMID 9878247.
Kitao S, Shimamoto A, Goto M, et al. (1999). "Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome.". Nat. Genet. 22 (1): 82-4. doi:10.1038/8788. PMID 10319867.
Yankiwski V, Marciniak RA, Guarente L, Neff NF (2000). "Nuclear structure in normal and Bloom syndrome cells.". Proc. Natl. Acad. Sci. U.S.A. 97 (10): 5214-9. doi:10.1073/pnas.090525897. PMID 10779560.
Kawabe T, Tsuyama N, Kitao S, et al. (2000). "Differential regulation of human RecQ family helicases in cell transformation and cell cycle.". Oncogene 19 (41): 4764-72. doi:10.1038/sj.onc.1203841. PMID 11032027.
Wang LL, Worley K, Gannavarapu A, et al. (2002). "Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome.". Am. J. Hum. Genet. 71 (1): 165-7. PMID 12016592.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932.
Roversi G, Beghini A, Zambruno G, et al. (2003). "Identification of two novel RECQL4exonic SNPs and genomic characterization of the IVS12 minisatellite.". J. Hum. Genet. 48 (2): 107-9. doi:10.1007/s100380300016. PMID 12601557.
Wang LL, Gannavarapu A, Clericuzio CL, et al. (2004). "Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patients.". Am. J. Med. Genet. A 118 (3): 299-301. doi:10.1002/ajmg.a.10057. PMID 12673665.
Beghini A, Castorina P, Roversi G, et al. (2004). "RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient.". Am. J. Med. Genet. A 120 (3): 395-9. doi:10.1002/ajmg.a.20154. PMID 12838562.
Siitonen HA, Kopra O, Kääriäinen H, et al. (2004). "Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases.". Hum. Mol. Genet. 12 (21): 2837-44. doi:10.1093/hmg/ddg306. PMID 12952869.
Brandenberger R, Wei H, Zhang S, et al. (2005). "Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation.". Nat. Biotechnol. 22 (6): 707-16. doi:10.1038/nbt971. PMID 15146197.
Nishijo K, Nakayama T, Aoyama T, et al. (2004). "Mutation analysis of the RECQL4 gene in sporadic osteosarcomas.". Int. J. Cancer 111 (3): 367-72. doi:10.1002/ijc.20269. PMID 15221963.
Yin J, Kwon YT, Varshavsky A, Wang W (2005). "RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway.". Hum. Mol. Genet. 13 (20): 2421-30. doi:10.1093/hmg/ddh269. PMID 15317757.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi:10.1101/gr.2596504. PMID 15489334.
Sengupta S, Shimamoto A, Koshiji M, et al. (2005). "Tumor suppressor p53 represses transcription of RECQ4 helicase.". Oncogene 24 (10): 1738-48. doi:10.1038/sj.onc.1208380. PMID 15674334.
Sangrithi MN, Bernal JA, Madine M, et al. (2005). "Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome.". Cell 121 (6): 887-98. doi:10.1016/j.cell.2005.05.015. PMID 15960976.