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RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

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Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific...
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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).
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DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
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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...
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Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
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Video Experimental Relacionado

Updated: May 1, 2026

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair
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gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair

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"La carrera" para clonar el BRCA1

Mary-Claire King1

  • 1Department of Medicine and Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA.

Science (New York, N.Y.)
|March 29, 2014
PubMed
Resumen
Este resumen es generado por máquina.

El descubrimiento del gen BRCA1 en 1990 revolucionó la investigación del cáncer de mama. Su posterior clonación en 1994 allanó el camino para avances en las estrategias de prevención y tratamiento.

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Área de la Ciencia:

  • Genética La genética.
  • Oncología Oncología.
  • Biología Molecular Biología Molecular

Sus antecedentes:

  • La existencia del gen del cáncer de mama humano 1 (BRCA1) se confirmó en 1990, localizando la susceptibilidad al cáncer de mama de inicio joven en el cromosoma 17q21.
  • Este descubrimiento dio inicio a una carrera científica de alto perfil para clonar y secuenciar el gen.

Objetivo del estudio:

  • Para conmemorar el 20 aniversario de la clonación posicional del gen BRCA1.
  • Para reflexionar sobre la "carrera" competitiva para identificar el gen BRCA1.
  • Para discutir las consecuencias a largo plazo del descubrimiento de BRCA1 en el cáncer de mama.

Principales métodos:

  • La clonación posicional del gen BRCA1.
  • Revisión de los acontecimientos históricos que rodean el descubrimiento del gen.
  • Análisis del impacto en la prevención y el tratamiento del cáncer de mama.

Principales resultados:

  • El gen BRCA1 fue clonado posicionalmente en septiembre de 1994.
  • El descubrimiento fue precedido por el mapeo de la predisposición al cáncer en el cromosoma 17q21.
  • Siguieron avances significativos en la investigación del cáncer de mama y en la práctica clínica.

Conclusiones:

  • La "carrera" para descubrir el BRCA1 aceleró el progreso científico.
  • La identificación de BRCA1 transformó la comprensión del cáncer de mama hereditario.
  • La investigación continua sobre BRCA1 es crucial para mejorar los resultados de los pacientes.