Редактирование: PI4KB

Phosphatidylinositol 4-kinase beta (EC 2.7.1.67) (PI4K-beta) (PI4Kbeta) (PtdIns 4-kinase beta) (NPIK) (PI4K92) (PI4KIII) [PIK4CB]

==Publications==

{{medline-entry
|title=Differential DNA Methylation in Relation to Age and Health Risks of Obesity.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26213922
|abstract=The aim of this study was to evaluate whether genome-wide levels of DNA methylation are associated with age and the health risks of obesity (HRO); defined according to BMI categories as "Low HRO" (overweight and class 1 obesity) versus "High HRO" (class 2 and class 3 obesity). Anthropometric measurements were assessed in a subsample of 48 volunteers from the Metabolic Syndrome Reduction in Navarra (RESMENA) study and 24 women from another independent study, Effects of Lipoic Acid and Eicosapentaenoic Acid in Human Obesity (OBEPALIP study). In the pooled population; the methylation levels of 55 CpG sites were significantly associated with age after Benjamini-Hochberg correction. In addition, DNA methylation of three CpG sites located in ELOVL2; [[HOXC4]] and [[PI4KB]] were further negatively associated with their mRNA levels. Although no differentially methylated CpG sites were identified in relation to HRO after multiple testing correction; several nominally significant CpG sites were identified in genes related to insulin signaling; energy and lipid metabolism. Moreover, statistically significant associations between BMI or mRNA levels and two HRO-related CpG sites located in GPR133 and [[ITGB5]] are reported. As a conclusion, these findings from two Spanish cohorts add knowledge about the important role of DNA methylation in the age-related regulation of gene expression. In addition; a relevant influence of age on DNA methylation in white blood cells was found, as well as, on a trend level, novel associations between DNA methylation and obesity. 
|mesh-terms=* Adult
* Aging
* CpG Islands
* DNA Methylation
* Female
* Gene Expression Regulation
* Health
* Humans
* Leukocytes
* Male
* Middle Aged
* Obesity
* Risk Factors
|keywords=* BMI
* ELOVL2
* GPR133
* ITGB5
* PI4KB
* PRKCZ
* epigenetics
* gene expression
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581172
}}
{{medline-entry
|title=Coordinated Expression of Phosphoinositide Metabolic Genes during Development and Aging of Human Dorsolateral Prefrontal Cortex.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26168237
|abstract=Phosphoinositides, lipid-signaling molecules, participate in diverse brain processes within a wide metabolic cascade. Gene transcriptional networks coordinately regulate the phosphoinositide cascade during human brain Development and Aging. We used the public BrainCloud database for human dorsolateral prefrontal cortex to examine age-related expression levels of 49 phosphoinositide metabolic genes during Development (0 to 20  years) and Aging (21  years). We identified three groups of partially overlapping genes in each of the two intervals, with similar intergroup correlations despite marked phenotypic differences between Aging and Development. In each interval, [[ITPKB]], [[PLCD1]], [[PIK3R3]], [[ISYNA1]], [[IMPA2]], [[INPPL1]], [[PI4KB]], and [[AKT1]] are in Group 1, [[PIK3CB]], [[PTEN]], [[PIK3CA]], and [[IMPA1]] in Group 2, and [[SACM1L]], PI3KR4, [[INPP5A]], [[SYNJ1]], and [[PLCB1]] in Group 3. Ten of the genes change expression nonlinearly during Development, suggesting involvement in rapidly changing neuronal, glial and myelination events. Correlated transcription for some gene pairs likely is facilitated by colocalization on the same chromosome band. Stable coordinated gene transcriptional networks regulate brain phosphoinositide metabolic pathways during human Development and Aging.
|mesh-terms=* Adolescent
* Adult
* Aging
* Child
* Child, Preschool
* Gene Expression
* Humans
* Infant
* Infant, Newborn
* Phosphatidylinositols
* Prefrontal Cortex
* Young Adult

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500567
}}