Werner syndrome ATP-dependent helicase

Werner syndrome ATP-dependent helicase

WRN (Werner syndrome) is a human gene that provides instructions for producing Werner protein, which is a type of enzyme called a helicase. Helicase enzymes generally unwind and separate double-stranded DNA. These activities are necessary before DNA can be copied in preparation for cell division (DNA replication). Helicase enzymes are also critical for making a blueprint of a gene for protein production, a process called transcription. Further evidence suggests that Werner protein plays a critical role in repairing DNA. Overall, this protein helps maintain the structure and integrity of a person's DNA.

The WRN gene is located on the short (p) arm of chromosome 8 between positions 12 and 11.2, from base pair 31,010,319 to base pair 31,150,818.

Related conditions

Werner syndrome is caused by mutations in the WRN gene. More than 20 mutations in the WRN gene are known to cause Werner syndrome. Many of these mutations result in an abnormally shortened Werner protein. Evidence suggests that the altered protein is not transported into the cell nucleus, where it normally interacts with DNA. This shortened protein may also be broken down too quickly, leading to a loss of Werner protein in the cell. Without normal Werner protein in the nucleus, cells cannot perform the tasks of DNA replication, repair, and transcription. Researchers are still determining how these mutations cause the appearance of premature aging seen in Werner syndrome.

References

*
*
*
*
*PBB_Further_reading
citations =
*cite journal | author=Moser MJ, Oshima J, Monnat RJ |title=WRN mutations in Werner syndrome. |journal=Hum. Mutat. |volume=13 |issue= 4 |pages= 271–9 |year= 1999 |pmid= 10220139 |doi=10.1002/(SICI)1098-1004(1999)13:4<271::AID-HUMU2>3.0.CO;2-Q |doilabel=10.1002/(SICI)1098-1004(1999)13:4271::AID-HUMU23.0.CO;2-Q
*cite journal | author=Kastan MB, Lim DS |title=The many substrates and functions of ATM. |journal=Nat. Rev. Mol. Cell Biol. |volume=1 |issue= 3 |pages= 179–86 |year= 2001 |pmid= 11252893 |doi= 10.1038/35043058

External links

* [http://www.genecards.org/cgi-bin/carddisp?WRN GeneCard]
* [http://www.wernersyndrome.org/ws_wrn.html Werner Syndrome Mutational Database]

PBB_Controls
update_page = yes
require_manual_inspection = no
update_protein_box = yes
update_summary = no
update_citations = no


Wikimedia Foundation. 2010.

Игры ⚽ Поможем решить контрольную работу

Look at other dictionaries:

  • Helicase — Structure of E. coli helicase RuvA Helicases are a class of enzymes vital to all living organisms. They are motor proteins that move directionally along a nucleic acid phosphodiester backbone, separating two annealed nucleic acid strands (i.e.,… …   Wikipedia

  • p53 — For the band and album of the same name, see P53 (band) and P53 (album). Tumor protein p53 PDB rendering based on 1TUP …   Wikipedia

  • Proliferating cell nuclear antigen — The assembled human DNA clamp, a trimer of the protein PCNA …   Wikipedia

  • Bloom syndrome protein — Bloom syndrome, also known as BLM, is a human gene. PBB Summary section title = summary text = The Bloom syndrome gene product is related to the RecQ subset of DExH box containing DNA helicases and has both DNA stimulated ATPase and ATP dependent …   Wikipedia

  • DNA-PKcs — Protein kinase, DNA activated, catalytic polypeptide Identifiers Symbols PRKDC; DNA PKcs; DNAPK; DNPK1; HYRC; HYRC1; XRCC7; p350 External IDs …   Wikipedia

  • Homologous recombination — Figure 1. During meiosis, homologous recombination can produce new combinations of genes as shown here between similar but not identical copies of human chromosome 1. Homologous recombination is a type of genetic recombination in which nucleotide …   Wikipedia

  • WRN — Helicasa dependiente de ATP del síndrome de Werner Estructura tridimensional de la proteína WRN. HUGO …   Wikipedia Español

  • Ku70 — Estructura tridimensional de la proteína Ku70. HUGO 4055 …   Wikipedia Español

  • Ku80 — Estructura tridimensional de la proteína Ku80. HUGO 12833 …   Wikipedia Español

  • DNA repair — For the journal, see DNA Repair (journal). DNA damage resulting in multiple broken chromosomes DNA repair refers to a collection of processes by which a cell identifies and corrects damage to the DNA molecules that encode its genome. In human… …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”