Jove
Visualize
Contáctanos
JoVE
x logofacebook logolinkedin logoyoutube logo
ACERCA DE JoVE
Visión GeneralLiderazgoBlogCentro de Ayuda JoVE
AUTORES
Proceso de PublicaciónConsejo EditorialAlcance y PolíticasRevisión por ParesPreguntas FrecuentesEnviar
BIBLIOTECARIOS
TestimoniosSuscripcionesAccesoRecursosConsejo Asesor de BibliotecasPreguntas Frecuentes
INVESTIGACIÓN
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchivo
EDUCACIÓN
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualCentro de Recursos para ProfesoresSitio de Profesores
Términos y Condiciones de Uso
Política de Privacidad
Políticas

Videos de Conceptos Relacionados

RNA Splicing01:32

RNA Splicing

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...
RNA Splicing01:32

RNA Splicing

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...
Alternative RNA Splicing02:18

Alternative RNA Splicing

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...
Pre-mRNA Processing: RNA Splicing01:32

Pre-mRNA Processing: RNA Splicing

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...
Alternative RNA Splicing02:18

Alternative RNA Splicing

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...
Transposons01:24

Transposons

Transposons, or "jumping genes," are small mobile genetic elements (MGEs) that range from 700 to 40,000 base pairs in length. They are found in all organisms and can move within the same chromosome or transfer to different chromosomes. In some cases, transposons can also jump between different host DNA molecules, such as plasmids or viruses, contributing to genetic variability.Barbara McClintock first discovered these mobile genetic elements in the 1940s while studying maize genetics, and she...

También podría leer

Artículos Relacionados

Artículos vinculados a este trabajo por autores compartidos, revista y gráfico de citas.

Ordenar por
Same author

Identification and characterization of HIV positive Ethiopian elite controllers in both Africa and Israel.

HIV medicine·2018
Same author

Assessing the function of homologous recombination DNA repair in malignant pleural effusion (MPE) samples.

British journal of cancer·2014
Same author

Transduction of CD34(+) and CD34(-)/lin(-) hemopoietic progenitors by lentivirus vectors.

Cytotherapy·2010
Same author

Toxoplasma co-opts host gene expression by injection of a polymorphic kinase homologue.

Nature·2006
Same author

Polymorphic secreted kinases are key virulence factors in toxoplasmosis.

Science (New York, N.Y.)·2006
Same author

Infection with Toxoplasma gondii bradyzoites has a diminished impact on host transcript levels relative to tachyzoite infection.

Infection and immunity·2006

Video Experimental Relacionado

Updated: Jul 13, 2026

Examination of the Telomere G-overhang Structure in Trypanosoma brucei
15:25

Examination of the Telomere G-overhang Structure in Trypanosoma brucei

Published on: January 26, 2011

Hay evidencia de trans splicing en los tripanosomas.

R E Sutton, J C Boothroyd

    Cell
    |November 21, 1986
    PubMed
    Resumen

    Los ARN mensajeros del tripanosoma (ARNm) se sintetizan mediante el empalme trans. Una pequeña molécula de ARN (medRNA) proporciona el mini-exón 5 ', que se empalma con los exones codificantes de proteínas, produciendo ARNm maduro y un producto de ARNm libre.

    Área de la Ciencia:

    • Biología Molecular Biología Molecular
    • Parasitología Parasitología.
    • ARN Biología Biología ARN

    Sus antecedentes:

    • Los ARNm del tripanosoma poseen una secuencia de miniexones de 5' conservada.
    • Este mini-exón se transcribe por separado del exón principal codificador de proteínas.

    Objetivo del estudio:

    • Para investigar el mecanismo de síntesis de ARNm en los tripanosomas.
    • Para probar la hipótesis del trans splicing para la maduración del ARNm.

    Principales métodos:

    • Análisis del ARN del tripanosoma para la presencia de minRNA.
    • Ensayos de desbranqueamiento in vitro con extractos de células HeLa.

    Principales resultados:

    • Se detectaron cantidades significativas de minARN libre en las preparaciones de ARN tripanosómico.

    Más Videos Relacionados

    High-throughput Gene Tagging in Trypanosoma brucei
    11:26

    High-throughput Gene Tagging in Trypanosoma brucei

    Published on: August 12, 2016

    Dissection of Drosophila melanogaster Flight Muscles for Omics Approaches
    08:33

    Dissection of Drosophila melanogaster Flight Muscles for Omics Approaches

    Published on: October 17, 2019

    Videos de Experimentos Relacionados

    Last Updated: Jul 13, 2026

    Examination of the Telomere G-overhang Structure in Trypanosoma brucei
    15:25

    Examination of the Telomere G-overhang Structure in Trypanosoma brucei

    Published on: January 26, 2011

    High-throughput Gene Tagging in Trypanosoma brucei
    11:26

    High-throughput Gene Tagging in Trypanosoma brucei

    Published on: August 12, 2016

    Dissection of Drosophila melanogaster Flight Muscles for Omics Approaches
    08:33

    Dissection of Drosophila melanogaster Flight Muscles for Omics Approaches

    Published on: October 17, 2019

  • minRNA podría ser liberado de las estructuras de ARN más grandes por una enzima de desbranqueamiento.
  • Conclusiones:

    • El transsplicing es el mecanismo fisiológico para generar ARNm maduro en los tripanosomas.
    • Este proceso implica la unión de un mini-exón de medRNA a los exones codificadores de proteínas.