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

Reproductive Cloning01:27

Reproductive Cloning

Reproductive cloning is the process of producing a genetically identical copy—a clone—of an entire organism. While clones can be produced by splitting an early embryo—similar to what happens naturally with identical twins—cloning of adult animals is usually done by a process called somatic cell nuclear transfer (SCNT).
Somatic Cell Nuclear Transfer
In SCNT, an egg cell is taken from an animal and its nucleus is removed, creating an enucleated egg. Then a somatic cell—any cell that is not a sex...
Cell Specific Gene Expression01:58

Cell Specific Gene Expression

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...
Reproductive Cloning01:27

Reproductive Cloning

Reproductive cloning is the process of producing a genetically identical copy—a clone—of an entire organism. While clones can be produced by splitting an early embryo—similar to what happens naturally with identical twins—cloning of adult animals is usually done by a process called somatic cell nuclear transfer (SCNT).
Somatic Cell Nuclear Transfer
In SCNT, an egg cell is taken from an animal and its nucleus is removed, creating an enucleated egg. Then a somatic cell—any cell that is not a sex...
Cell Specific Gene Expression01:58

Cell Specific Gene Expression

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...
Introduction to Nuclear Reprogramming01:14

Introduction to Nuclear Reprogramming

Nuclear reprogramming is the process of switching gene expression of one cell type to that of another cell type, usually from a differentiated cell state to an undifferentiated cell state. Differentiation occurs during processes such as development and morphogenesis, tissue regeneration, and malignancy. Cells can also be artificially induced to reprogram their gene expression by techniques such as nuclear transfer, induced pluripotency, and cell fusion. Such techniques have many applications in...
Cloning of Dolly the Sheep01:08

Cloning of Dolly the Sheep

The first successfully cloned mammal was Dolly, a sheep, born on 5th July 1996 at Roslin Institute, Scotland. The cloned sheep was named after the American singer Dolly Parton. Dolly lived for seven years and died of respiratory complications, which is speculated to be due to the actual age of her DNA. Because the DNA in cloned cells belongs to an older individual,  the cloned individual’s life expectancy may be affected. Indeed, analysis of Dolly’s DNA revealed shorter telomeres than other...

You might also read

Related Articles

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

Sort by
Same author

In-hospital Outcome of Pharmaco-Invasive (Tenecteplase) versus Primary PCI Strategy in Patients with ST-Elevated Myocardial Infarction in a Tertiary Care Hospital.

Mymensingh medical journal : MMJ·2026
Same author

Diabetes distress and depression are independently associated with gastrointestinal symptoms in type 2 diabetes in Bangladesh.

Diabetic medicine : a journal of the British Diabetic Association·2024
Same author

Knowledge, Attitude and Practice of Undergraduate Medical Students of Bangladesh Regarding COVID-19 and its Vaccination.

Mymensingh medical journal : MMJ·2023
Same author

First Direct Measurement Constraining the ^{34}Ar(α,p)^{37}K Reaction Cross Section for Mixed Hydrogen and Helium Burning in Accreting Neutron Stars.

Physical review letters·2023
Same author

The study of healthcare professionals' perspective towards the quality of diabetic care services in Abha.

European review for medical and pharmacological sciences·2023
Same author

Mutations in the bone morphogenetic protein 15 gene causing defective protein secretion in Cholistani infertile sheep.

Brazilian journal of biology = Revista brasleira de biologia·2022

Related Experiment Video

Updated: Jun 30, 2026

In vivo Reprogramming of Adult Somatic Cells to Pluripotency by Overexpression of Yamanaka Factors
12:12

In vivo Reprogramming of Adult Somatic Cells to Pluripotency by Overexpression of Yamanaka Factors

Published on: December 17, 2013

Gene expression in cloned bovine fetal liver.

A D Schrader1, M J Iqbal, K L Jones

  • 1Department of Animal Science, Food and Nutrition, Southern Illinois University, Carbondale, Illinois, USA.

Cloning and Stem Cells
|April 26, 2003
PubMed
Summary

Nuclear transfer (NT) in cattle is inefficient, causing developmental issues. This study investigated differential gene expression in NT fetuses but found no significant gene expression differences in liver tissues.

Area of Science:

  • Animal Reproduction
  • Developmental Biology
  • Genetics

Background:

  • Nuclear transfer (NT) bypasses fertilization for gene propagation but suffers from low efficiency.
  • Common NT issues include large birth weights and physical abnormalities in organs like the liver, heart, and brain.
  • The underlying causes of these anomalies, potentially linked to nuclear reprogramming, remain largely unknown.

Purpose of the Study:

  • To detect and identify differential gene expression in the livers of nuclear transfer (NT) fetuses compared to embryo transfer (ET) derived fetuses.
  • To investigate the role of precise nuclear reprogramming in NT success rates.
  • To identify specific genes affected by the NT process in cattle.

Main Methods:

  • Established a non-clonal cell line from an Angus fetus for NT donor cells.

More Related Videos

Functional Cloning Using a Xenopus Oocyte Expression System
09:40

Functional Cloning Using a Xenopus Oocyte Expression System

Published on: January 30, 2016

Transcriptome Profiling of In-Vivo Produced Bovine Pre-implantation Embryos Using Two-color Microarray Platform
09:04

Transcriptome Profiling of In-Vivo Produced Bovine Pre-implantation Embryos Using Two-color Microarray Platform

Published on: January 30, 2017

Related Experiment Videos

Last Updated: Jun 30, 2026

In vivo Reprogramming of Adult Somatic Cells to Pluripotency by Overexpression of Yamanaka Factors
12:12

In vivo Reprogramming of Adult Somatic Cells to Pluripotency by Overexpression of Yamanaka Factors

Published on: December 17, 2013

Functional Cloning Using a Xenopus Oocyte Expression System
09:40

Functional Cloning Using a Xenopus Oocyte Expression System

Published on: January 30, 2016

Transcriptome Profiling of In-Vivo Produced Bovine Pre-implantation Embryos Using Two-color Microarray Platform
09:04

Transcriptome Profiling of In-Vivo Produced Bovine Pre-implantation Embryos Using Two-color Microarray Platform

Published on: January 30, 2017

  • Utilized Differential Display Reverse Transcription Polymerase Chain Reaction (ddRT-PCR) to screen for differentially expressed genes.
  • Sequenced identified Expressed Sequence Tags (ESTs) and verified gene expression via semi-quantitative RT-PCR.
  • Main Results:

    • Identified 39 potential differentially expressed genes/ESTs using ddRT-PCR.
    • Sequenced 23 Bos taurus ESTs and submitted them to GenBank.
    • Semi-quantitative RT-PCR analysis of 15 genes did not reveal significant expression differences between NT and ET fetuses.

    Conclusions:

    • While ddRT-PCR suggested potential differential gene expression, subsequent verification failed to confirm significant differences in liver tissues.
    • The study did not identify specific genes responsible for NT-associated anomalies in the analyzed liver samples.
    • Further research is needed to elucidate the genetic factors influencing nuclear reprogramming and developmental outcomes in nuclear transfer.