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

lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

10.1K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
10.1K
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

3.8K
3.8K
Insulin: Biosynthesis, Chemistry, and Preparation01:25

Insulin: Biosynthesis, Chemistry, and Preparation

1.9K
The endoplasmic reticulum (ER) of pancreatic β-cells synthesizes preproinsulin, which consists of a signal peptide, A and B chains, and a C-peptide. Preproinsulin is then cleaved and folded into proinsulin, which translocates to the Golgi apparatus for sorting and packaging into secretory granules. In these granules, enzymatic clipping generates insulin and C-peptide.
Damage or functional impairment of β-cells inhibits insulin production, leading to diabetes. Diabetes treatment...
1.9K
Insulin Secretory Vesicles01:05

Insulin Secretory Vesicles

7.3K
Insulin secretory vesicles release insulin to stimulate blood glucose uptake and regulate carbohydrate metabolism. When the blood glucose levels increase, glucose enters the pancreatic β-islet cells through glucose transporters. Once inside, glucose is metabolized through glycolysis, the citric acid cycle, and the electron transport chain, producing ATP. This increase in ATP concentration closes ATP-sensitive potassium channels, leading to depolarization of the membrane and the opening of...
7.3K
Cell Specific Gene Expression01:58

Cell Specific Gene Expression

16.9K
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...
16.9K
Insulin: The Receptor and Signaling Pathways01:28

Insulin: The Receptor and Signaling Pathways

5.9K
Insulin action is mediated through a receptor tyrosine kinase, akin to the IGF-1 receptor. The number of receptors per cell varies significantly, from 40 on erythrocytes to 300,000 on adipocytes and hepatocytes. The insulin receptor consists of linked α/β subunit dimers, forming a heterotetramer glycoprotein with two extracellular α subunits and two β subunits spanning the membrane. The α subunits inhibit the inherent tyrosine kinase activity of the β subunits, but...
5.9K

You might also read

Related Articles

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

Sort by
Same author

High-purity stem cell-derived β-cells recapitulate key transcriptional and functional features of human islets.

bioRxiv : the preprint server for biology·2026
Same author

CHD4 and NKX2.2 Cooperate to Regulate β-Cell Function by Repressing Non-β-Cell Gene Programs.

Diabetes·2026
Same author

Regulatory elements in the Sox9 locus license the initiation of pancreatic ductal adenocarcinoma.

Cell reports·2026
Same author

Optimizing Single-Cell Long-Read Sequencing for Enhanced Isoform Detection in Pancreatic Islets.

Diabetes·2026
Same author

Independent control of neurogenesis and dorsoventral patterning by NKX2-2.

Genes & development·2026
Same author

Human NKX2.2 influences islet endocrine cell fate choices through regulation of WNT pathway genes.

bioRxiv : the preprint server for biology·2025

Related Experiment Video

Updated: Mar 24, 2026

Surgical Injury to the Mouse Pancreas through Ligation of the Pancreatic Duct as a Model for Endocrine and Exocrine Reprogramming and Proliferation
07:44

Surgical Injury to the Mouse Pancreas through Ligation of the Pancreatic Duct as a Model for Endocrine and Exocrine Reprogramming and Proliferation

Published on: August 7, 2015

17.1K

βlinc1 encodes a long noncoding RNA that regulates islet β-cell formation and function.

Luis Arnes1, Ildem Akerman2, Dina A Balderes1

  • 1Department of Genetics and Development, Columbia University, New York, New York 10032, USA;

Genes & Development
|March 6, 2016
PubMed
Summary

A newly discovered long noncoding RNA, βlinc1, is essential for pancreatic beta cell development and function. Its absence disrupts insulin production and glucose homeostasis, leading to diabetes-like conditions in mice.

Keywords:
long noncoding RNApancreas developmentβ cell

More Related Videos

Single-cell RNA Sequencing and Analysis of Human Pancreatic Islets
11:34

Single-cell RNA Sequencing and Analysis of Human Pancreatic Islets

Published on: July 18, 2019

17.3K
RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level
11:04

RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level

Published on: May 19, 2019

10.6K

Related Experiment Videos

Last Updated: Mar 24, 2026

Surgical Injury to the Mouse Pancreas through Ligation of the Pancreatic Duct as a Model for Endocrine and Exocrine Reprogramming and Proliferation
07:44

Surgical Injury to the Mouse Pancreas through Ligation of the Pancreatic Duct as a Model for Endocrine and Exocrine Reprogramming and Proliferation

Published on: August 7, 2015

17.1K
Single-cell RNA Sequencing and Analysis of Human Pancreatic Islets
11:34

Single-cell RNA Sequencing and Analysis of Human Pancreatic Islets

Published on: July 18, 2019

17.3K
RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level
11:04

RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level

Published on: May 19, 2019

10.6K

Area of Science:

  • Endocrinology
  • Molecular Biology
  • Genetics

Background:

  • Pancreatic beta cells regulate glucose homeostasis; their dysfunction causes diabetes mellitus.
  • Long noncoding RNAs (lncRNAs) are implicated in development and disease, but their role in pancreas development is largely unexplored.
  • In vivo investigation of lncRNAs in pancreatic beta cell development is lacking.

Purpose of the Study:

  • To investigate the in vivo role of lncRNAs in pancreas development.
  • To identify specific lncRNAs crucial for pancreatic beta cell specification and function.
  • To elucidate the regulatory mechanisms of identified lncRNAs in beta cell development.

Main Methods:

  • In vivo studies in mouse models.
  • Genetic deletion of the βlinc1 gene.
  • Analysis of islet development and beta cell function.
  • Assessment of glucose homeostasis.
  • Investigation of gene regulation by βlinc1.

Main Results:

  • βlinc1 (beta-cell long intergenic noncoding RNA 1), a conserved lncRNA, is essential for pancreatic beta cell specification and function.
  • βlinc1 coordinates the regulation of multiple islet-specific transcription factors.
  • Deletion of βlinc1 leads to impaired islet development.
  • Loss of βlinc1 disrupts glucose homeostasis in adult mice.

Conclusions:

  • βlinc1 is a critical regulator of pancreatic beta cell development and function.
  • βlinc1 acts by coordinating the expression of key islet transcription factors.
  • Dysregulation of βlinc1 contributes to diabetes mellitus by impairing beta cell function and glucose homeostasis.