TY - JOUR
T1 - Exon structure and flanking intronic sequences of the human RET proto-oncogene
AU - Ceccherini, Isabella
AU - Bocciardi, Renata
AU - Luo, Yin
AU - Pasini, Barbara
AU - Hofstra, Robert
AU - Takahashi, Masahide
AU - Romeo, Giovanni
PY - 1993/11/15
Y1 - 1993/11/15
N2 - Using a PCR strategy based on an initial set of 15 couples of primers designed from the known cDNA sequence, we identified 18 introns in the human RET proto-oncogene and sequenced the corresponding 5' and 3' exon-intron junctions. This approach was successful in locating all the introns contained in fragments short enough to be amplified by PCR. Thus 19 exons were identified which, together with the previously reported exon subjected to alternative splicing, brings the total number of RET exons to 20. This information is relevant for the screening of recently reported missense mutations of RET which cause Multiple Endocrine Neoplasia 2A (MEN2A) and for the search of additional point mutations of the same gene which might cause two other neural crest disorders, MEN2B and Hirschsprung disease, mapping in the same region as MEN2A.
AB - Using a PCR strategy based on an initial set of 15 couples of primers designed from the known cDNA sequence, we identified 18 introns in the human RET proto-oncogene and sequenced the corresponding 5' and 3' exon-intron junctions. This approach was successful in locating all the introns contained in fragments short enough to be amplified by PCR. Thus 19 exons were identified which, together with the previously reported exon subjected to alternative splicing, brings the total number of RET exons to 20. This information is relevant for the screening of recently reported missense mutations of RET which cause Multiple Endocrine Neoplasia 2A (MEN2A) and for the search of additional point mutations of the same gene which might cause two other neural crest disorders, MEN2B and Hirschsprung disease, mapping in the same region as MEN2A.
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U2 - 10.1006/bbrc.1993.2392
DO - 10.1006/bbrc.1993.2392
M3 - Article
C2 - 7902707
AN - SCOPUS:0027371670
SN - 0006-291X
VL - 196
SP - 1288
EP - 1295
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -