Inositol pyrophosphates modulate cell cycle independently of alteration in telomere length. (January 2016)
- Record Type:
- Journal Article
- Title:
- Inositol pyrophosphates modulate cell cycle independently of alteration in telomere length. (January 2016)
- Main Title:
- Inositol pyrophosphates modulate cell cycle independently of alteration in telomere length
- Authors:
- Banfic, Hrvoje
Crljen, Vladiana
Lukinovic-Skudar, Vesna
Dembitz, Vilma
Lalic, Hrvoje
Bedalov, Antonio
Visnjic, Dora - Abstract:
- Abstract: Synthesis of inositol pyrophosphates through activation of Kcs1 plays an important role in the signalling response required for cell cycle progression after mating pheromone arrest. Overexpression of Kcs1 doubled the level of inositol pyrophosphates when compared to wild type cells and 30 min following the release from α-factor block further increase in inositol pyrophosphates was observed, which resulted that cells overexpressing Kcs1 reached G2 /M phase earlier than wild type cells. Similar effect was observed in ipk1Δ cells, which are unable to synthesize IP6 -derived inositol pyrophosphates (IP7 and IP8 ) but will synthesize IP5 -derived inositol pyrophosphates (PP-IP4 and (PP)2 -IP3 ). Although ipk1Δ cells have shorter telomeres than wild type cells, overexpression of Kcs1 in both strains have similar effect on cell cycle progression. As it is known that PP-IP4 regulates telomere length through Tel1, inositol polyphosphates, cell cycle and telomere length were determined in tel1Δ cells. The release of the cells from α-factor block and overexpression of Kcs1 in tel1Δ cells produced similar effects on inositol pyrophosphates level and cell cycle progression when compared to wild type cells, although tel1Δ cells possesses shorter telomeres than wild type cells. It can be concluded that telomere length does not affect cell cycle progression, since cells with short telomeres ( ipk1Δ and tel1Δ ) progress through cell cycle in a similar manner as wild type cells andAbstract: Synthesis of inositol pyrophosphates through activation of Kcs1 plays an important role in the signalling response required for cell cycle progression after mating pheromone arrest. Overexpression of Kcs1 doubled the level of inositol pyrophosphates when compared to wild type cells and 30 min following the release from α-factor block further increase in inositol pyrophosphates was observed, which resulted that cells overexpressing Kcs1 reached G2 /M phase earlier than wild type cells. Similar effect was observed in ipk1Δ cells, which are unable to synthesize IP6 -derived inositol pyrophosphates (IP7 and IP8 ) but will synthesize IP5 -derived inositol pyrophosphates (PP-IP4 and (PP)2 -IP3 ). Although ipk1Δ cells have shorter telomeres than wild type cells, overexpression of Kcs1 in both strains have similar effect on cell cycle progression. As it is known that PP-IP4 regulates telomere length through Tel1, inositol polyphosphates, cell cycle and telomere length were determined in tel1Δ cells. The release of the cells from α-factor block and overexpression of Kcs1 in tel1Δ cells produced similar effects on inositol pyrophosphates level and cell cycle progression when compared to wild type cells, although tel1Δ cells possesses shorter telomeres than wild type cells. It can be concluded that telomere length does not affect cell cycle progression, since cells with short telomeres ( ipk1Δ and tel1Δ ) progress through cell cycle in a similar manner as wild type cells and that overexpression of Kcs1 in cells with either short or normal telomeres will increase S phase progression without affecting telomere length. Furthermore, IP5 -derived inositol pyrophosphates can compensate for the loss of IP6 -derived inositol pyrophosphates, in modulating S phase progression of the cell cycle. … (more)
- Is Part Of:
- Advances in biological regulation. Volume 60(2016)
- Journal:
- Advances in biological regulation
- Issue:
- Volume 60(2016)
- Issue Display:
- Volume 60, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 60
- Issue:
- 2016
- Issue Sort Value:
- 2016-0060-2016-0000
- Page Start:
- 22
- Page End:
- 28
- Publication Date:
- 2016-01
- Subjects:
- Inositol pyrophosphates -- Kcs1 -- Ipk1 -- Tel1 -- Telomere length -- Cell cycle
Plc phospholipase C -- IP3 inositol trisphosphate -- IP4 inositol tetrakisphosphate -- IP5 inositol pentakisphosphate -- IP6 inositol hexakisphosphate -- IP7 (also referred as PP-IP5) diphosphoinositol pentakisphosphate -- IP8 [also referred as (PP)2-IP4] bisdiphosphoinositol tetrakisphosphate -- PP-IP4 diphosphoinositol tetrakisphosphate -- (PP)2-IP3 bisdiphosphoinositol trisphosphate -- HPLC high performance liquid chromatography
Cellular control mechanisms -- Periodicals
Biological control systems -- Periodicals
Molecular biology -- Periodicals
Periodicals
571.74 - Journal URLs:
- http://www.sciencedirect.com/science/journal/22124926 ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.jbior.2015.09.003 ↗
- Languages:
- English
- ISSNs:
- 2212-4926
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8031.xml