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Novel processing in a mammalian nuclear 28S pre‐rRNA: tissue‐specific elimination of an ‘intron’ bearing a hidden break site
Author(s) -
Melen Gustavo J.,
Pesce C.Gustavo,
Rossi María Susana,
Kornblihtt Alberto R.
Publication year - 1999
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/18.11.3107
Subject(s) - biology , intron , bearing (navigation) , genetics , ribosomal rna , computational biology , microbiology and biotechnology , gene , cartography , geography
Splitting and apparent splicing of ribosomal RNA, both previously unknown in vertebrates, were found in rodents of the genus Ctenomys . Instead of being formed by a single molecule of 4.4 kb, 28S rRNA is split in two molecules of 2.6 and 1.8 kb. A hidden break, mapping within a 106 bp ‘intron’ located in the D6 divergent region, is expressed in mature ribosomes of liver, lung, heart and spleen, as well as in primary fibroblast cultures. Testis‐specific processing eliminates the intron and concomitantly the break site, producing non‐split 28S rRNA molecules exclusively in this organ. The intron is flanked by two 9 bp direct repeats, revealing the acquisition by insertion of a novel rRNA processing strategy in the evolution of higher organisms.