TY - JOUR
T1 - Nested introns in an intron
T2 - Evidence of multi-step splicing in a large intron of the human dystrophin pre-mRNA
AU - Suzuki, Hitoshi
AU - Kameyama, Toshiki
AU - Ohe, Kenji
AU - Tsukahara, Toshifumi
AU - Mayeda, Akila
N1 - Funding Information:
We would like to thank Dr. A. Malhotra for providing purified recombinant RNase R; Drs. G.R. Screaton, J. Wang and M.Q. Zhang for their helps in the initial stages of this study; Drs. M.P. Deutscher, K.E. Rudd and A.R. Krainer for their valuable suggestions and encouragement; and T. Venkataraman for technical assistance. A.M. was supported by a Developmental Grant from the Muscular Dystrophy Association and a Grant-in-Aid for Challenging Exploratory Research from Japan Society for the Promotion of Science (JSPS) . H.S. was supported in part by a Grant-in-Aid for Young Scientists (B) from the JSPS , and in part by an Intramural Research Grant (22–5) for Neurological and Psychiatric Disorders of NCNP.
PY - 2013/3/18
Y1 - 2013/3/18
N2 - The mechanisms by which huge human introns are spliced out precisely are poorly understood. We analyzed large intron 7 (110 199 nucleotides) generated from the human dystrophin (DMD) pre-mRNA by RT-PCR. We identified branching between the authentic 5′ splice site and the branch point; however, the sequences far from the branch site were not detectable. This RT-PCR product was resistant to exoribonuclease (RNase R) digestion, suggesting that the detected lariat intron has a closed loop structure but contains gaps in its sequence. Transient and concomitant generation of at least two branched fragments from nested introns within large intron 7 suggests internal nested splicing events before the ultimate splicing at the authentic 5′ and 3′ splice sites. Nested splicing events, which bring the authentic 5′ and 3′ splice sites into close proximity, could be one of the splicing mechanisms for the extremely large introns.
AB - The mechanisms by which huge human introns are spliced out precisely are poorly understood. We analyzed large intron 7 (110 199 nucleotides) generated from the human dystrophin (DMD) pre-mRNA by RT-PCR. We identified branching between the authentic 5′ splice site and the branch point; however, the sequences far from the branch site were not detectable. This RT-PCR product was resistant to exoribonuclease (RNase R) digestion, suggesting that the detected lariat intron has a closed loop structure but contains gaps in its sequence. Transient and concomitant generation of at least two branched fragments from nested introns within large intron 7 suggests internal nested splicing events before the ultimate splicing at the authentic 5′ and 3′ splice sites. Nested splicing events, which bring the authentic 5′ and 3′ splice sites into close proximity, could be one of the splicing mechanisms for the extremely large introns.
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U2 - 10.1016/j.febslet.2013.01.057
DO - 10.1016/j.febslet.2013.01.057
M3 - Article
C2 - 23395799
AN - SCOPUS:84875230031
SN - 0014-5793
VL - 587
SP - 555
EP - 561
JO - FEBS Letters
JF - FEBS Letters
IS - 6
ER -