作者: V. L. van Santen , R. A. Spritz
关键词: Exonic splicing enhancer 、 Genetics 、 Precursor mRNA 、 Sequence (medicine) 、 Biology 、 RNA splicing 、 Cell biology 、 Splice site mutation 、 splice 、 Gene 、 Protein splicing
摘要: To define the extent of intervening sequence required for splicing higher eukaryotic mRNA precursors in vivo, we constructed deletions within second human G gamma-globin gene that progressively approach donor or acceptor splice sites. Most can be deleted with no effect on splicing. At site, 6 bases are sufficient accurate and efficient 20 splicing, 16 but at a reduced level. However, 15 insufficient significant The ending near site is independent whether an A-G dinucleotide introduced into region by deletion.