Distinct versus redundant properties among members of the INK4 family of cyclin-dependent kinase inhibitors
(2000) In FEBS Letters 470(2). p.161-166- Abstract
- p16(INK4a), p15(INK4b), p18(INK4c) and p19(INK4d) comprise a family of cyclin-dependent kinase inhibitors and tumor suppressors. We report that the INK4 proteins share the ability to arrest cells in G1, and interact with CDK4 or CDK6 with similar avidity. In contrast, only p18 and particularly p19 are phosphorylated in vivo, and each of the human INK4 proteins shows unique expression patterns dependent on cell and tissue type, and differentiation stage. Thus, the INK4 proteins harbor redundant as well as non-overlapping properties, suggesting distinct regulatory modes, and diverse roles for the individual INK4 family members in cell cycle control, cellular differentiation, and multistep oncogenesis.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1782575
- author
- Thullberg, M ; Bartkova, J ; Khan, S ; Hansen, Klaus ; Rönnstrand, Lars LU ; Lukas, Jiri ; Strauss, M and Bartek, Jiri
- publishing date
- 2000
- type
- Contribution to journal
- publication status
- published
- subject
- in
- FEBS Letters
- volume
- 470
- issue
- 2
- pages
- 161 - 166
- publisher
- Wiley-Blackwell
- external identifiers
-
- scopus:0034708554
- ISSN
- 1873-3468
- language
- English
- LU publication?
- no
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Experimental Clinical Chemistry (013016010)
- id
- b2a67523-154b-4110-b87d-d4d2c3cbaf13 (old id 1782575)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/10734227
- http://www.sciencedirect.com/science/article/pii/S0014579300013077
- date added to LUP
- 2016-04-04 09:39:26
- date last changed
- 2022-01-29 18:54:14
@article{b2a67523-154b-4110-b87d-d4d2c3cbaf13, abstract = {{p16(INK4a), p15(INK4b), p18(INK4c) and p19(INK4d) comprise a family of cyclin-dependent kinase inhibitors and tumor suppressors. We report that the INK4 proteins share the ability to arrest cells in G1, and interact with CDK4 or CDK6 with similar avidity. In contrast, only p18 and particularly p19 are phosphorylated in vivo, and each of the human INK4 proteins shows unique expression patterns dependent on cell and tissue type, and differentiation stage. Thus, the INK4 proteins harbor redundant as well as non-overlapping properties, suggesting distinct regulatory modes, and diverse roles for the individual INK4 family members in cell cycle control, cellular differentiation, and multistep oncogenesis.}}, author = {{Thullberg, M and Bartkova, J and Khan, S and Hansen, Klaus and Rönnstrand, Lars and Lukas, Jiri and Strauss, M and Bartek, Jiri}}, issn = {{1873-3468}}, language = {{eng}}, number = {{2}}, pages = {{161--166}}, publisher = {{Wiley-Blackwell}}, series = {{FEBS Letters}}, title = {{Distinct versus redundant properties among members of the INK4 family of cyclin-dependent kinase inhibitors}}, url = {{http://www.ncbi.nlm.nih.gov/pubmed/10734227}}, volume = {{470}}, year = {{2000}}, }