Literature DB >> 16575159

Complementation hypothesis: the necessity of a monoallelic gene expression mechanism in mammalian development.

T Kaneko-Ishino1, T Kohda, R Ono, F Ishino.   

Abstract

Gene expression from both parental alleles (biallelic expression) is beneficial in minimizing the occurrence of recessive genetic disorders in diploid organisms. However, imprinted genes in mammals display parent of origin-specific monoallelic expression. As some imprinted genes play essential roles in mammalian development, the reason why mammals adopted the genomic imprinting mechanism has been a mystery since its discovery. In this review, based on the recent studies on imprinted gene regulation we discuss several advantageous features of a monoallelic expression mechanism and the necessity of genomic imprinting in the current mammalian developmental system. We further speculate how the present genomic imprinting system has been established during mammalian evolution by the mechanism of complementation between paternal and maternal genomes under evolutionary pressure predicted by the genetic conflict hypothesis. 2006 S. Karger AG, Basel.

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Year:  2006        PMID: 16575159     DOI: 10.1159/000090811

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  14 in total

1.  Polymorphism of DLK1 and CLPG gene and their association with phenotypic traits in Chinese cattle.

Authors:  F Y Chen; H Niu; J Q Wang; C Z Lei; X Y Lan; C L Zhang; M J Li; L S Hua; J Wang; H Chen
Journal:  Mol Biol Rep       Date:  2010-03-30       Impact factor: 2.316

Review 2.  Mammalian genomic imprinting.

Authors:  Marisa S Bartolomei; Anne C Ferguson-Smith
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-07-01       Impact factor: 10.005

Review 3.  The origin and evolution of genomic imprinting and viviparity in mammals.

Authors:  Marilyn B Renfree; Shunsuke Suzuki; Tomoko Kaneko-Ishino
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2013-01-05       Impact factor: 6.237

4.  Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14.

Authors:  Melita D Irving; Karin Buiting; Deniz Kanber; Celia Donaghue; Reiner Schulz; Amaka Offiah; Shehla N Mohammed; Rebecca J Oakey
Journal:  Am J Med Genet A       Date:  2010-08       Impact factor: 2.802

Review 5.  Imprinting evolution and human health.

Authors:  Radhika Das; Daniel D Hampton; Randy L Jirtle
Journal:  Mamm Genome       Date:  2009-10-15       Impact factor: 2.957

Review 6.  Origin of Sex-Biased Mental Disorders: An Evolutionary Perspective.

Authors:  Rama S Singh; Karun K Singh; Shiva M Singh
Journal:  J Mol Evol       Date:  2021-02-25       Impact factor: 2.395

7.  Possible imprinting and microchimerism in chronic lymphocytic leukemia and related lymphoproliferative disorders.

Authors:  Viggo Jønsson; Geir E Tjønnfjord; Tom B Johannesen; Sven Ove Samuelsen; Bernt Ly
Journal:  Transl Oncogenomics       Date:  2008-02-10

8.  Retrotransposon silencing by DNA methylation can drive mammalian genomic imprinting.

Authors:  Shunsuke Suzuki; Ryuichi Ono; Takanori Narita; Andrew J Pask; Geoffrey Shaw; Changshan Wang; Takashi Kohda; Amber E Alsop; Jennifer A Marshall Graves; Yuji Kohara; Fumitoshi Ishino; Marilyn B Renfree; Tomoko Kaneko-Ishino
Journal:  PLoS Genet       Date:  2007-04-13       Impact factor: 5.917

9.  The role of genes domesticated from LTR retrotransposons and retroviruses in mammals.

Authors:  Tomoko Kaneko-Ishino; Fumitoshi Ishino
Journal:  Front Microbiol       Date:  2012-07-27       Impact factor: 5.640

10.  Expression and protein localisation of IGF2 in the marsupial placenta.

Authors:  Eleanor I Ager; Andrew J Pask; Geoff Shaw; Marilyn B Renfree
Journal:  BMC Dev Biol       Date:  2008-02-20       Impact factor: 1.978

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