Allelic expression of IGF2 in marsupials and birds

被引:158
作者
O'Neill, MJ
Ingram, RS
Vrana, PB
Tilghman, SM [1 ]
机构
[1] Princeton Univ, Howard Hughes Med Inst, Princeton, NJ 08544 USA
[2] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
关键词
D O I
10.1007/PL00008182
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Genomic imprinting, the parent-of-origin-specific expression of genes, has been observed in a variety of eutherian mammals. One gene that has been shown to be imprinted in all eutherians examined is the IGF2 gene. This gene encodes a potent fetal-specific growth factor that is expressed almost exclusively from the paternal chromosome. Several other imprinted genes in the IGF2 pathway are imprinted as well, suggesting that IGF2 is a focal point for the selective pressure leading to imprinted gene expression. This observation is in keeping with a proposal that imprinting arose as the result of a genetic conflict between parents over the allocation of maternal resources to the embryo. One prediction of this model is that imprinting exists in species in which there is at least some contribution of maternal resources to the embryo, and in which polyandry is observed. To test this prediction the allelic expression of the IGF2 gene was examined in two noneutherian species. The IGF2 gene was shown to be expressed in a paternal-specific manner identical to that in eutherians in Monodelphis domestica, a placental South American opossum. In contrast, the IGF2 gene is biallelic in expression in chickens, which are oviparous, and make no postfertilization contribution of maternal resources to the offspring.
引用
收藏
页码:18 / 20
页数:3
相关论文
共 16 条
  • [1] THE MOUSE INSULIN-LIKE GROWTH-FACTOR TYPE-2 RECEPTOR IS IMPRINTED AND CLOSELY LINKED TO THE TME LOCUS
    BARLOW, DP
    STOGER, R
    HERRMANN, BG
    SAITO, K
    SCHWEIFER, N
    [J]. NATURE, 1991, 349 (6304) : 84 - 87
  • [2] Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
    Brown, KW
    Villar, AJ
    Bickmore, W
    ClaytonSmith, J
    Catchpoole, D
    Maher, ER
    Reik, W
    [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (12) : 2027 - 2032
  • [3] PHOSPHOGLYCERATE KINASE POLYMORPHISM IN KANGAROOS PROVIDES FURTHER EVIDENCE FOR PATERNAL-X INACTIVATION
    COOPER, DW
    VANDEBER.JL
    SHARMAN, GB
    POOLE, WE
    [J]. NATURE-NEW BIOLOGY, 1971, 230 (13): : 155 - &
  • [4] Nucleotide sequence and genomic structure of the chicken insulin-like growth factor-II (IGF-II) coding region
    Darling, DC
    Brickell, PM
    [J]. GENERAL AND COMPARATIVE ENDOCRINOLOGY, 1996, 102 (03) : 283 - 287
  • [5] A GROWTH-DEFICIENCY PHENOTYPE IN HETEROZYGOUS MICE CARRYING AN INSULIN-LIKE GROWTH FACTOR-II GENE DISRUPTED BY TARGETING
    DECHIARA, TM
    EFSTRATIADIS, A
    ROBERTSON, EJ
    [J]. NATURE, 1990, 345 (6270) : 78 - 80
  • [6] PARENTAL IMPRINTING OF THE MOUSE INSULIN-LIKE GROWTH FACTOR-II GENE
    DECHIARA, TM
    ROBERTSON, EJ
    EFSTRATIADIS, A
    [J]. CELL, 1991, 64 (04) : 849 - 859
  • [7] Genomic imprinting in ruminants: allele-specific gene expression in parthenogenetic sheep
    Feil, R
    Khosla, S
    Cappai, P
    Loi, P
    [J]. MAMMALIAN GENOME, 1998, 9 (10) : 831 - 834
  • [8] PARENTAL GENOMIC IMPRINTING OF THE HUMAN IGF2 GENE
    GIANNOUKAKIS, N
    DEAL, C
    PAQUETTE, J
    GOODYER, CG
    POLYCHRONAKOS, C
    [J]. NATURE GENETICS, 1993, 4 (01) : 98 - 101
  • [9] PARENT-SPECIFIC GENE-EXPRESSION AND THE TRIPLOID ENDOSPERM
    HAIG, D
    WESTOBY, M
    [J]. AMERICAN NATURALIST, 1989, 134 (01) : 147 - 155
  • [10] Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene
    Miyoshi, N
    Kuroiwa, Y
    Kohda, T
    Shitara, H
    Yonekawa, H
    Kawabe, T
    Hasegawa, H
    Barton, SC
    Surani, MA
    Kaneko-Ishino, T
    Ishino, F
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (03) : 1102 - 1107