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Calmodulin-dependent Signaling01:16

Calmodulin-dependent Signaling

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Calmodulin (CaM) is a calcium-binding protein in eukaryotes that controls various calcium-regulated cellular processes. It has four calcium-binding sites that bind calcium to form the calcium-calmodulin ( Ca2+-CaM) complex. GPCR stimulation increases the calcium levels in the cells that bind to CaM and induces a conformational change.
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Calcium is an essential signaling molecule required for various cellular functions. Calcium pumps and ion channels on cell and organellar membranes, such as those on the endoplasmic reticulum (ER), regulate calcium concentrations inside the cell. They remain closed, keeping the cytosolic calcium levels low at a resting state.
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Multicellular organisms contain a variety of structurally and functionally distinct cell types, but the DNA in all the cells originated from the same parent cells. The differences in the cells can be attributed to the differential gene expression. Liver cells, whose functions include detoxification of blood, production of bile to metabolize fats, and synthesis of proteins essential for metabolism, must express a specific set of genes to perform their functions. Gene expression also varies with...
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Wnt is a zygotic effect gene that is expressed during very early embryonic development. It regulates various processes in animals starting from early development through the adult stage, such as organogenesis in the embryo and maintenance of neuronal and blood stem cells. Wnt proteins can induce a wide variety of intracellular pathways depending upon the specific abilities of different Wnt ligands to form a complex with shared and cognate receptors in the presence of different co-receptors. The...
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Amplifying Signals via Second Messengers01:15

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Many receptor binding ligands are hydrophilic; they do not cross the cell membrane but bind to cell-surface receptors. Thus, their message must be relayed by second messengers present in the cell cytoplasm. There are several second messenger pathways, each with its own way of relaying information. For example, the G protein-coupled receptors can activate both phosphoinositol and cyclic AMP (cAMP) second messenger pathways. The phosphoinositol pathway is active when the receptor induces...
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Related Experiment Video

Updated: Jan 5, 2026

Fluorescent Calcium Imaging and Subsequent In Situ Hybridization for Neuronal Precursor Characterization in Xenopus laevis
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Calcium Signaling and Gene Expression.

Basant K Puri1

  • 1CAR, Cambridge, UK. bpuri@cantab.net.

Advances in Experimental Medicine and Biology
|October 25, 2019
PubMed
Summary
This summary is machine-generated.

Calcium signaling regulates gene expression at multiple levels, influencing neuronal plasticity and potentially offering therapeutic targets for cancer by reactivating tumor suppressor genes.

Keywords:
AMPA receptorsAlternative splicing patternsCalcium signalingEpigenetic regulationGene expressionGene reactivationL-type voltage-gated calcium channelsNMDA receptorsTranscriptionTranslation

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Area of Science:

  • Neuroscience
  • Molecular Biology
  • Cell Biology

Background:

  • Calcium signaling is a critical cellular process involved in gene expression.
  • It plays a key role in mammalian neuronal synaptic plasticity.
  • Dysregulation of calcium signaling is implicated in various diseases.

Purpose of the Study:

  • To elucidate the multifaceted roles of calcium signaling in gene expression.
  • To explore calcium signaling's impact on transcriptional, post-transcriptional, and translational regulation.
  • To investigate the potential of targeting calcium signaling for therapeutic interventions.

Main Methods:

  • Analysis of calcium influx pathways including NMDA receptors, AMPA receptors, and voltage-gated calcium channels.
  • Investigation of downstream signaling cascades such as Rac1, CaMKK, CaMKI, Ras, and MAPK/ERK.
  • Examination of post-transcriptional modifications like alternative splicing and translational regulation involving proteins like YB-1 and TG2.
  • Exploration of calcium's role in epigenetic modifications.

Main Results:

  • Calcium influx via NMDA and AMPA receptors activates distinct signaling pathways that modulate gene expression.
  • Signaling molecules translocate to the nucleus to alter genes involved in synaptic plasticity.
  • Calcium signaling influences alternative splicing, notably in the GRIN1 transcript.
  • Regulation of translation is mediated by proteins like TG2 and YB-1.
  • Calcium signaling impacts epigenetic regulation, including DNA methylation patterns.

Conclusions:

  • Calcium signaling is a crucial regulator of gene expression across transcriptional, post-transcriptional, and translational levels.
  • These regulatory mechanisms are fundamental to neuronal synaptic plasticity.
  • Targeting calcium signaling presents a promising therapeutic strategy, particularly for cancer treatment through epigenetic reactivation of tumor suppressor genes.