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  2. Exon trapping - Wikipedia

    en.wikipedia.org/wiki/Exon_trapping

    The genomic fragment is inserted into the intron of a 'splicing vector' consisting of a known exon - intron - exon sequence of DNA, and the vector is then inserted into an eukaryotic cell. If the fragment does not contain exons (i.e., consists solely of intron DNA), it will be spliced out together with the vector's original intron.

  3. Intron - Wikipedia

    en.wikipedia.org/wiki/Intron

    An intron is any nucleotide sequence within a gene that is not expressed or operative in the final RNA product. The word intron is derived from the term intragenic region, i.e., a region inside a gene. [1] The term intron refers to both the DNA sequence within a gene and the corresponding RNA sequence in RNA transcripts. [2]

  4. Alternative splicing - Wikipedia

    en.wikipedia.org/wiki/Alternative_splicing

    Intron retention: A sequence may be spliced out as an intron or simply retained. This is distinguished from exon skipping because the retained sequence is not flanked by introns . If the retained intron is in the coding region, the intron must encode amino acids in frame with the neighboring exons, or a stop codon or a shift in the reading ...

  5. RNA splicing - Wikipedia

    en.wikipedia.org/wiki/RNA_splicing

    The word intron is derived from the terms intragenic region, [1] and intracistron, [2] that is, a segment of DNA that is located between two exons of a gene.The term intron refers to both the DNA sequence within a gene and the corresponding sequence in the unprocessed RNA transcript.

  6. Exon - Wikipedia

    en.wikipedia.org/wiki/Exon

    An exon is any part of a gene that will form a part of the final mature RNA produced by that gene after introns have been removed by RNA splicing. The term exon refers to both the DNA sequence within a gene and to the corresponding sequence in RNA transcripts.

  7. Exome sequencing - Wikipedia

    en.wikipedia.org/wiki/Exome_sequencing

    It consists of two steps: the first step is to select only the subset of DNA that encodes proteins. These regions are known as exons—humans have about 180,000 exons, constituting about 1% of the human genome, or approximately 30 million base pairs. The second step is to sequence the exonic DNA using any high-throughput DNA sequencing ...

  8. Exon shuffling - Wikipedia

    en.wikipedia.org/wiki/Exon_shuffling

    Exon shuffling is a molecular mechanism for the formation of new genes. It is a process through which two or more exons from different genes can be brought together ectopically , or the same exon can be duplicated , to create a new exon-intron structure. [ 1 ]

  9. Minigene - Wikipedia

    en.wikipedia.org/wiki/Minigene

    A minigene is a minimal gene fragment that includes an exon and the control regions necessary for the gene to express itself in the same way as a wild type gene fragment. This is a minigene in its most basic sense. More complex minigenes can be constructed containing multiple exons and intron(s).