cDNA sequence and genomic structure of the rat RET proto-oncogene

被引:9
|
作者
Matera, I
Miguel-Rodríguez, MD
Fernández-Santos, JM
Santamaria, G
Puliti, A
Ravazzolo, R
Romeo, G
Galera-Davidson, H
Ceccherini, I
机构
[1] Ist Giannina Gaslini, Genet Mol Lab, I-16148 Genoa, Italy
[2] Univ Seville, Fac Med, Dept Anat Patol, E-41009 Seville, Spain
[3] Univ Pisa, Dipartimento Sci Uomo & Ambiente, I-56100 Pisa, Italy
[4] Univ Genoa, Dipartimento Oncol Biol & Genet, I-16100 Genoa, Italy
[5] Int Agcy Res Canc, Genet Canc Susceptibil Unit, F-69372 Lyon, France
来源
DNA SEQUENCE | 2000年 / 11卷 / 05期
关键词
RET proto-oncogene; rat; RT-PCR; DNA sequence; genomic structure;
D O I
10.3109/10425170009033991
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The RET proto-oncogene, a member of the Receptor Tyrosine Kinase family, plays a crucial role during the development of the excretory system and the enteric nervous system, as demonstrated by in vivo animal studies and by its involvement in the pathogenesis of several human neurocristopathies like Hirschsprung disease and Multiple Endocrine Neoplasia type 2. Using a multistep RT-PCR approach we have isolated and sequenced the cDNA of the whole rat RET proto-oncogene, reporting the deduced amino acid sequence in comparison with the human and mouse counterparts. Moreover, two different isoforms (RET9 and RET51) have been confirmed in the rat, while a third RET isoform demonstrated in human (RET43) has not resulted to be conserved in this species. Finally, we have determined the genomic structure of the rat RET proto-oncogene comparing the exon-intron boundaries and intron sizes with the known structure of the human homologous gene. Our findings will facilitate the molecular study of appropriate rat models of RET related human diseases.
引用
收藏
页码:405 / 417
页数:13
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