The biological effects of simple tandem repeats: Lessons from the repeat expansion diseases: Table 1.
Author(s) -
Karen Usdin
Publication year - 2008
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.070409.107
Subject(s) - biology , tandem repeat , genetics , intergenic region , direct repeat , genome , gene , computational biology , trinucleotide repeat expansion , alternative splicing , rna splicing , human genome , exon , rna , allele
Tandem repeats are common features of both prokaryote and eukaryote genomes, where they can be found not only in intergenic regions but also in both the noncoding and coding regions of a variety of different genes. The repeat expansion diseases are a group of human genetic disorders caused by long and highly polymorphic tandem repeats. These disorders provide many examples of the effects that such repeats can have on many biological processes. While repeats in the coding sequence can result in the generation of toxic or malfunctioning proteins, noncoding repeats can also have significant effects including the generation of chromosome fragility, the silencing of the genes in which they are located, the modulation of transcription and translation, and the sequestering of proteins involved in processes such as splicing and cell architecture.
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