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Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols
Published on: June 6, 2017
Transcriptional profiling of the cell cycle checkpoint gene krüppel-like factor 4 reveals a global inhibitory
Erika M Whitney1, Amr M Ghaleb, Xinming Chen
1Division of Digestive Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA.
Abstract:
Krüppel-like factor 4 (KLF4; also known as gut-enriched Krüppel-like factor or GKLF) is known to exhibit checkpoint function during the G1/S and G2/M transitions of the cell cycle. The mechanism by which KLF4 exerts these effects is not fully established. Here we investigated the expression profile of KLF4 in an inducible system over a time course of 24 h. Using oligonucleotide microarrays, we determined that the fold changes relative to control in expression levels of KLF4 exhibited a time-dependent increase from 3- to 20-fold between 4 and 24 h following KLF4 induction. During this period and among a group of 473 cell cycle regulatory genes examined, 96 were positively correlated and 86 were negatively correlated to KLF4's expression profile. Examples of upregulated cell cycle genes include those encoding tumor suppressors such as MCC and FHIT, and cell cycle inhibitors such as CHES1 and CHEK1. Examples of downregulated genes include those that promote the cell cycle including several cyclins and those required for DNA replication. Unexpectedly, several groups of genes involved in macromolecular synthesis, including protein biosynthesis, transcription, and cholesterol biosynthesis, were also significantly inhibited by KLF4. Thus, KLF4 exerts a global inhibitory effect on macromolecular biosynthesis that is beyond its established role as a cell cycle inhibitor.
Insights
Krüppel-like factor 4 (KLF4) inhibits cell cycle progression and unexpectedly suppresses macromolecular biosynthesis. This study reveals KLF4’s broader role beyond cell cycle regulation, impacting gene expression and cellular processes.
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Background:
- Krüppel-like factor 4 (KLF4) is recognized for its role in cell cycle checkpoint control.
- The precise mechanisms underlying KLF4's regulatory functions remain incompletely understood.
Purpose of the Study:
- To investigate the temporal expression profile of KLF4.
- To identify genes regulated by KLF4 during cell cycle transitions.
- To elucidate the broader impact of KLF4 on cellular biosynthesis.
Main Methods:
- Utilized an inducible system to study KLF4 expression over a 24-hour time course.
- Employed oligonucleotide microarrays to analyze gene expression changes.
- Correlated KLF4 expression levels with a panel of 473 cell cycle regulatory genes.
Main Results:
- KLF4 expression increased 3- to 20-fold between 4 and 24 hours post-induction.
- KLF4 positively and negatively correlated with 96 and 86 cell cycle genes, respectively.
- KLF4 significantly inhibited genes involved in macromolecular synthesis, including protein and cholesterol biosynthesis.
Conclusions:
- KLF4 demonstrates a time-dependent increase in expression, correlating with significant alterations in cell cycle gene expression.
- KLF4 exerts a global inhibitory effect on macromolecular biosynthesis, extending beyond its known cell cycle inhibitory functions.
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