MCM4

MCM4

A gene on chromosome 8q12-q13 that encodes one of the highly conserved mini-chromosome maintenance (MCM) proteins that are involved in initiating eukaryotic genome replication. The hexameric protein complex formed by MCM2-7 is a key component of the pre-replication complex, and may be involved in forming replication forks and in recruiting other DNA replication related proteins; it is required for the entry in S phase and for cell division. The sub-complex formed by MCM2, MCM4, MCM6 and MCM7 regulates the complex’s helicase activity. MCM4 phosphorylation by CDC2 kinase reduces the helicase activity and chromatin binding of the MCM complex.
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Request for quotations : side projection control unit component mcm4 stand, cat.
Side Projection Control Unit Component Mcm4 Stand, Cat. No. 10046869 Complete With Prefilter, Cat No. 05892380 For The Angiographic Complex Manufactured By Siemens Ag Medical Solution Groups, Axiom Artis Dbc, Serial No. 44146, Manufactured By Sieme
qRT-PCR analysis confirmed that the mRNA levels of cyclin family members ( ccna1 , ccnb1 , ccnd1 , and cdk1 ), minichromosome maintenance proteins ( cdc45 , mcm2 , mcm3 , mcm4 , mcm5 , mcm6 , and mcm7 ), and proliferation cell nuclear antigen ( PCNA ) were significantly upregulated in ATF3-overexpressing CFs [Figure 3]a.
Cardiac Fibroblast-Specific Activating Transcription Factor 3 Promotes Myocardial Repair after Myocardial Infarction
Comparison between G2 versus G3, which evaluated the influence of T2D with good glycemic control, showed that the HLA-DQA1 (p =<0.0001) and HLA-DQB1 (p = <0.0001) genes were upregulated and the MCM4 and SEC13 genes were downregulated DEGs in G2 subjects (p = 00006 and p = 0008, resp., Figure 1(c)).
When comparing the well-controlled T2D (G2) patients versus normoglycemics (G3), besides the aforementioned HLA-DQB1 gene, we found that SEC13 and MCM4 genes presented downregulation in both microarray and RTqPCR.
Expression Profile of Genes Potentially Associated with Adequate Glycemic Control in Patients with Type 2 Diabetes Mellitus
Ki-67 expression is superior to mitotic count and novel proliferation markers PHH3, MCM4 and mitosin as a prognostic factor in thick cutaneous melanoma.
Immunohistochemistry in Dermatopathology
Samples were collected at 6 m (MCM1 and MCM7) and 9 m (MCM2 and MCM8) in Lake Fryxell and 13 m (MCM3 and MCM5) and 18 m (MCM4 and MCM6) in Lake WLB to capture the microbiology of distinct vertical physicochemical and biogeochemical layers within the trophogenic zone (region where adequate light exists to support phytoplankton photosynthesis) of the two lakes.
For example, in MCM4 and MCM6 samples (i.e., 18-m Lake WLB) where the salinity was higher than 80 PSU (~2X seawater) and oxygen was low (Table 1), Chao2 estimated and observed richness were both similar to or slightly higher than the less extreme samples (Fig.
Ciliate diversity, community structure, and novel taxa in lakes of the McMurdo Dry Valleys, Antarctica
Supporting the above findings, a recent in vivo licensing assay has proved that the concentration of chromatin bound MCM2 and MCM4 changes with progression of G1 phase and they fail to colocalize with other replication machinery [49].
MCM paradox: abundance of eukaryotic replicative helicases and genomic integrity
One example is the increased expression of the stem cell gene MCM4, which is involved in the control of DNA replication.
Gene signature helps predict melanoma outcome
(MCM4) should be given to all children at the 11-12 year old visit as
Recommended childhood and adolescent immunization schedule: United States * 2006
Minichromosome maintenance protein 2 (MCM2), which is in the same functional family as two other genes (MCM4 and MCM6) identified in the study of Chen et al.
Panel of genes transcriptionally up-regulated in squamous cell carcinoma of the cervix identified by representational difference analysis, confirmed by macroarray, and validated by real-time quantitative reverse transcription-PCR
We found that genes required for the replication of chromosomal DNA (PCNA, FEN1, CDC6, MCM2, MCM3, MCM4, MCM5, ORC1, ORC6, RRM1, RRM2) and genes required for postreplicative phases of the cell division cycle (e.g., CCNB1, PLK1) are coordinately induced and reach maximal expression levels between 8 and 24 hr (Figure 6B), consistent with the timing of the histologic changes observed in Figure 6A.
Phenotypic anchoring of gene expression changes during estrogen-induced uterine growth

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