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  2. Exon - Wikipedia

    en.wikipedia.org/wiki/Exon

    Across all eukaryotic genes in GenBank, there were (in 2002), on average, 5.48 exons per protein coding gene. The average exon encoded 30-36 amino acids. [7] While the longest exon in the human genome is 11555 bp long, several exons have been found to be only 2 bp long. [8] A single-nucleotide exon has been reported from the Arabidopsis genome. [9]

  3. 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 ...

  4. RNA splicing - Wikipedia

    en.wikipedia.org/wiki/RNA_splicing

    This results in a mature messenger RNA with a missing section of an exon. In this way, a point mutation, which might otherwise affect only a single amino acid, can manifest as a deletion or truncation in the final protein. [citation needed] Intron Exon Boundary in pre-mRNA 1 - 3' Splice site 2 - Poly pyrimidine Tract 3 - Branch site 4 - 5 ...

  5. 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 ]

  6. Intron - Wikipedia

    en.wikipedia.org/wiki/Intron

    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] The non-intron sequences that become joined by this RNA processing to form the mature RNA are called exons. [3]

  7. Splice site mutation - Wikipedia

    en.wikipedia.org/wiki/Splice_site_mutation

    The mutation must occur at the specific site at which intron splicing occurs: within non-coding sites in a gene, directly next to the location of the exon. The mutation can be an insertion, deletion, frameshift, etc. The splicing process itself is controlled by the given sequences, known as splice-donor and splice-acceptor sequences, which ...

  8. Gene expression - Wikipedia

    en.wikipedia.org/wiki/Gene_expression

    During the process of splicing, an RNA-protein catalytical complex known as spliceosome catalyzes two transesterification reactions, which remove an intron and release it in form of lariat structure, and then splice neighbouring exons together. [11] In certain cases, some introns or exons can be either removed or retained in mature mRNA. [12]

  9. Exon skipping - Wikipedia

    en.wikipedia.org/wiki/Exon_skipping

    Exon skipping is used to restore the reading frame within a gene. Genes are the genetic instructions for creating a protein, and are composed of introns and exons.Exons are the sections of DNA that contain the instruction set for generating a protein; they are interspersed with non-coding regions called introns.