STRUCTURE DETERMINATION AND EVOLUTION OF THE CHICKEN CDNA AND GENE ENCODING PREPROPANCREATIC POLYPEPTIDE

被引:13
|
作者
NATA, K [1 ]
SUGIMOTO, T [1 ]
KOHRI, K [1 ]
HIDAKA, H [1 ]
HATTORI, E [1 ]
YAMAMOTO, H [1 ]
YONEKURA, H [1 ]
OKAMOTO, H [1 ]
机构
[1] TOHOKU UNIV,SCH MED,DEPT BIOCHEM,2-1 SEIRYOU MACHI,AOBA KU,SENDAI,MIYAGI 980,JAPAN
关键词
MOSAIC EVOLUTION; NEUROPEPTIDE-Y; PEPTIDE-YY; NUCLEOTIDE SEQUENCE; CLONING; EXON; INTRON; RECOMBINANT DNA;
D O I
10.1016/0378-1119(93)90418-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have previously demonstrated that the C-terminal regions of the rat and human pancreatic polypeptide (PPP) precursors exhibit a high degree of divergence, whereas the N-terminal regions are highly conserved. This blend of structural conservation and divergence in the precursors appears to be caused by splice junction sliding and translational frameshift in the 3'-region of the PPP gene [Yonekura et al., J. Biol. Chem. 263 (1988) 2990-2997]. In the present study, we determined the nucleotide (nt) sequences of the chicken PPP (cPPP) cDNA and gene, and compared them with those of the mammals. In cPPP, the C-terminal region of the precursor is quite heterologous with respect to the rat (rPPP) and human (hPPP) precursors, and this heterogeneity is accentuated by the large deletion in exon 3 of cPPP. Furthermore, mutational accumulation during evolution caused the structural organization of the 3'-region of cPPP to change; cPPP is terminated in exon 3, whereas rPPP and hPPP are terminated in exon 4. Thus, our previous observation regarding the possibility of 'mosaic evolution' [Yamamoto et al., J. Biol. Chem. 261 (1986) 6156-6159] of PPP has been extended and confirmed by this study. Available evidence suggests that 'mosaic evolution' is a phenomenon unique to PPP, and not to the genes encoding the other members of the PPP family, neuropeptide-Y and peptide-YY.
引用
收藏
页码:183 / 189
页数:7
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