Ancient divergence of insulin and insulin-like growth factor

被引:67
作者
McRory, JE [1 ]
Sherwood, NM [1 ]
机构
[1] UNIV VICTORIA,DEPT BIOL,VICTORIA,BC V8W 2Y2,CANADA
关键词
D O I
10.1089/dna.1997.16.939
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Studies on the evolutionary pathway of the insulin gene family suggest that insulin and insulin-like growth factor (IGF) became distinct molecules only after the vertebrates arose. A single molecule with identity to both insulin and IGF was reported in amphioxus, To study the origin of insulin, we selected tunicates because their ancestors are thought to be a nodal point in the evolution of vertebrates, This is the first report of separate insulin and IGF molecules from invertebrates, Two cDNAs were isolated from the tunicate Chelyosoma productum: One cDNA encodes a distinct preproinsulin with B, C, and A domains, whereas the other encodes tunicate preproIGF, including all five domains in their proper sequence. Both mRNAs are expressed in the nervous system, digestive tract, heart, and possibly the gonad but not in branchial basket or tunic, Hence, insulin and igf genes have similar expression patterns. In situ, methods confirm the polymerase chain reaction evidence that tunicate insulin and igf mRNAs are expressed in cortical cells of the neural ganglion, We conclude that insulin and IGF have maintained separate gene lineages in both vertebrate and protochordate evolution and, thus, a distinct evolutionary history of more than 600 million years.
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收藏
页码:939 / 949
页数:11
相关论文
共 39 条
  • [1] ADACHI T, 1989, J BIOL CHEM, V264, P7681
  • [2] ADHAM IM, 1993, J BIOL CHEM, V268, P26668
  • [3] INSULIN IN THE BRAIN
    BASKIN, DG
    FIGLEWICZ, DP
    WOODS, SC
    PORTE, D
    DORSA, DM
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 1987, 49 : 335 - 347
  • [4] SEQUENCE OF A CDNA CLONE ENCODING HUMAN PREPROINSULIN-LIKE GROWTH FACTOR-II
    BELL, GI
    MERRYWEATHER, JP
    SANCHEZPESCADOR, R
    STEMPIEN, MM
    PRIESTLEY, L
    SCOTT, J
    RALL, LB
    [J]. NATURE, 1984, 310 (5980) : 775 - 777
  • [5] BEVIS PJR, 1978, CELL TISSUE RES, V187, P153
  • [6] BIRNBOIM HC, 1983, METHOD ENZYMOL, V100, P243
  • [7] MUTANTS OF HUMAN INSULIN-LIKE GROWTH FACTOR-I WITH REDUCED AFFINITY FOR THE TYPE-1 INSULIN-LIKE GROWTH-FACTOR RECEPTOR
    CASCIERI, MA
    CHICCHI, GG
    APPLEBAUM, J
    HAYES, NS
    GREEN, BG
    BAYNE, ML
    [J]. BIOCHEMISTRY, 1988, 27 (09) : 3229 - 3233
  • [8] EVOLUTION OF THE INSULIN SUPERFAMILY - CLONING OF A HYBRID INSULIN INSULIN-LIKE GROWTH-FACTOR CDNA FROM AMPHIOXUS
    CHAN, SJ
    CAO, QP
    STEINER, DF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (23) : 9319 - 9323
  • [9] CONSTRUCTION AND SELECTION OF RECOMBINANT PLASMIDS CONTAINING FULL-LENGTH COMPLEMENTARY DNAS CORRESPONDING TO RAT INSULIN-I AND INSULIN-II
    CHAN, SJ
    NOYES, BE
    AGARWAL, KL
    STEINER, DF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (10) : 5036 - 5040
  • [10] SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION
    CHOMCZYNSKI, P
    SACCHI, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) : 156 - 159