Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

RNA Splicing01:32

RNA Splicing

56.6K
Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
56.6K
Alternative RNA Splicing02:18

Alternative RNA Splicing

21.5K
Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
21.5K
What is Gene Expression?01:36

What is Gene Expression?

8.8K
A gene is a stretch of DNA that serves as the blueprint for functional RNAs and proteins. Since DNA is comprised  of nucleotides and proteins are comprised of amino acids, a mediator is required to convert the information encoded in DNA into proteins. This mediator is the messenger RNA (mRNA). mRNA copies the blueprint from DNA by a process called transcription. In eukaryotes, transcription occurs in the nucleus by complementary base-pairing with the DNA template. The mRNA is then...
8.8K
Transducer Mechanism: Nuclear Receptors01:31

Transducer Mechanism: Nuclear Receptors

1.4K
Nuclear receptors, or NRs, are unique transcription factors that regulate gene transcription and affect the cellular pathways involved in reproduction, development, or metabolism. Their ability to be stimulated by small lipophilic ligands and control vital cellular processes makes them ideal drug targets. Nearly 10-15% of currently prescribed drugs target these receptors.
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
1.4K
Chromatin Structure Regulates pre-mRNA Processing02:41

Chromatin Structure Regulates pre-mRNA Processing

7.1K
In eukaryotic cells, nascent mRNA transcripts need to undergo many post-transcriptional modifications to reach the cell cytoplasm and translate into functional proteins. For a long time, transcription and pre-mRNA processing were considered two independent events that occur sequentially in the cell. However, it has now been well established that transcription and pre-mRNA processing are two simultaneous processes that are precisely regulated inside the cell.
The chromatin structure, especially...
7.1K
Intracellular Hormone Receptors01:08

Intracellular Hormone Receptors

55.7K
Lipid-soluble hormones diffuse across the plasma and nuclear membrane of target cells to bind to their specific intracellular receptors. These receptors act as transcription factors that regulate gene expression and protein synthesis in the target cell
55.7K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Adrenergic modulation of melanocortin pathway by hunger signals.

Nature communications·2023
Same author

Hypomorphism of a Novel Long ERα Isoform Causes Severe Reproductive Dysfunctions in Female Mice.

Endocrinology·2022
Same author

Melanocortin MC<sub>4</sub>R receptor is required for energy expenditure but not blood pressure effects of angiotensin II within the mouse brain.

Physiological genomics·2022
Same author

An estrogen-sensitive hypothalamus-midbrain neural circuit controls thermogenesis and physical activity.

Science advances·2022
Same author

Activation of hypothalamic AgRP and POMC neurons evokes disparate sympathetic and cardiovascular responses.

American journal of physiology. Heart and circulatory physiology·2020
Same author

Celastrol Reduces Obesity in MC4R Deficiency and Stimulates Sympathetic Nerve Activity Affecting Metabolic and Cardiovascular Functions.

Diabetes·2019

Related Experiment Video

Updated: Aug 5, 2025

Detecting the Ligand-binding Domain Dimerization Activity of Estrogen Receptor Alpha Using the Mammalian Two-Hybrid Assay
09:07

Detecting the Ligand-binding Domain Dimerization Activity of Estrogen Receptor Alpha Using the Mammalian Two-Hybrid Assay

Published on: December 19, 2018

6.4K

Estrogen Receptor Alpha Splice Variants, Post-Translational Modifications, and Their Physiological Functions.

Kenji Saito1, Huxing Cui1,2,3

  • 1Department of Neuroscience and Pharmacology, Carver College of Medicine, The University of Iowa, Iowa City, IA 52241, USA.

Cells
|March 29, 2023
PubMed
Summary

Estrogen receptor alpha (ERα) has complex gene regulation, including splicing and post-translational modifications (PTMs). These variants impact ERα signaling in various tissues and physiological processes.

Keywords:
estrogen receptor alphamutant mouse modelspost-translational modificationssplicing isoforms

More Related Videos

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition
11:48

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition

Published on: October 9, 2014

13.0K
Systems Biology of Metabolic Regulation by Estrogen Receptor Signaling in Breast Cancer
10:36

Systems Biology of Metabolic Regulation by Estrogen Receptor Signaling in Breast Cancer

Published on: March 17, 2016

10.5K

Related Experiment Videos

Last Updated: Aug 5, 2025

Detecting the Ligand-binding Domain Dimerization Activity of Estrogen Receptor Alpha Using the Mammalian Two-Hybrid Assay
09:07

Detecting the Ligand-binding Domain Dimerization Activity of Estrogen Receptor Alpha Using the Mammalian Two-Hybrid Assay

Published on: December 19, 2018

6.4K
Detection of Alternative Splicing During Epithelial-Mesenchymal Transition
11:48

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition

Published on: October 9, 2014

13.0K
Systems Biology of Metabolic Regulation by Estrogen Receptor Signaling in Breast Cancer
10:36

Systems Biology of Metabolic Regulation by Estrogen Receptor Signaling in Breast Cancer

Published on: March 17, 2016

10.5K

Area of Science:

  • Endocrinology
  • Molecular Biology
  • Genetics

Background:

  • Estrogenic signaling is crucial for reproduction, metabolism, and cognitive functions.
  • Estrogen receptor alpha (ERα) mediates key cellular estrogenic effects.
  • ERα gene regulation involves complex transcription, splicing, and expression patterns.

Purpose of the Study:

  • To review the functional diversity of ERα splicing isoforms and post-translational modifications (PTMs).
  • To explore the role of these ERα variants in normal physiological processes.
  • To highlight findings from transgenic mouse models.

Main Methods:

  • Literature review focusing on ERα gene regulation.
  • Analysis of studies on ERα splicing variants and PTMs.
  • Examination of data from transgenic mouse models.

Main Results:

  • Differential splicing of ERα generates isoforms with varying molecular weights and functions.
  • PTMs further modulate ERα localization, ligand affinity, and activity.
  • Tissue-specific expression of ERα variants suggests distinct physiological roles.

Conclusions:

  • Understanding ERα splicing isoforms and PTMs is essential for comprehending normal physiology.
  • ERα variants can mediate specific signaling pathways, potentially antagonizing full-length ERα.
  • Further research is needed to elucidate the associations between ERα splicing, PTMs, and physiological functions.