Literature DB >> 16201410

Transgene transmission to progeny by oMt1a-oGH transgenic mice.

A D Thomas1, J D Murray, A M Oberbauer.   

Abstract

Most studies utilizing transgenic technology focus on the impact to traits of interest, rather than propagation of the transgene to offspring. In animals containing growth hormone constructs, transgene transmission to progeny follows a Mendelian pattern of inheritance in the first few generations following generation of a founder animal, but decreases in subsequent generations. In the present study, the ovine metallothionein 1a-ovine growth hormone (oMt1a-oGH) transgenic mouse was used to determine whether transgene transmission rate to progeny was affected by overexpression of ovine growth hormone in the transgenic parent. The oMt1a-oGH mouse is a useful model for assessing transgene transmission, as the construct is easily regulatable and transgene inactivation results in a return of plasma GH to basal levels. Male and female hemizygous oMt1a-oGH mice were assigned to 1 of 3 treatment groups: (1) mice never actively expressing the transgene, (2) mice actively expressing the transgene from 3 weeks of age, and (3) mice actively expressing the transgene from 3 to 11 (males) or 3 to 8 (females) weeks of age. Transgenic mice were mated to wild type animals and the resulting progeny were genotyped. Males never actively expressing the transgene passed on the transgene to progeny in a Mendelian fashion, while males actively expressing the transgene transmitted the transgene to a smaller than expected number of progeny. However, following inactivation of the oMt1a-oGH construct in transgenic males, subsequent offspring demonstrated Mendelian inheritance of the transgene. In contrast, females expressing the transgene from 3 to 8 weeks of age were able to pass on the oMt1a-oGH construct in a Mendelian fashion, but females from other treatment groups were not. In oMt1a-oGH males, reduced transgene transmission appears to be due to selection against transgenic gametes. In females, however, selection against the transgenic genotype likely occurs at the embryonic level.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16201410     DOI: 10.1007/s11248-005-4349-y

Source DB:  PubMed          Journal:  Transgenic Res        ISSN: 0962-8819            Impact factor:   2.788


  33 in total

1.  Regulation of expression of a sheep metallothionein 1a-sheep growth hormone fusion gene in transgenic mice.

Authors:  C M Shanahan; N W Rigby; J D Murray; J T Marshall; C A Townrow; C D Nancarrow; K A Ward
Journal:  Mol Cell Biol       Date:  1989-12       Impact factor: 4.272

2.  Behavior of transgenic mouse spermatozoa with galline protamine.

Authors:  M Maleszewski; S Kuretake; D Evenson; H Yanagimachi; J Bjordahl; R Yanagimachi
Journal:  Biol Reprod       Date:  1998-01       Impact factor: 4.285

3.  Correlated responses to selection for large body size in oMt1a-oGH transgenic mice: reproductive traits.

Authors:  K R Parks; E J Eisen; I J Parker; L G Hester; J D Murray
Journal:  Genet Res       Date:  2000-04       Impact factor: 1.588

4.  Sperm chromatin integrity of bucks transgenic for the WAP bGH gene.

Authors:  P Gogol; M Bochenek; Z Smorag
Journal:  Anim Reprod Sci       Date:  2000-12-01       Impact factor: 2.145

5.  Effects of expression of human or bovine growth hormone genes on sperm production and male reproductive performance in four lines of transgenic mice.

Authors:  A Bartke; E M Naar; L Johnson; M R May; M Cecim; J S Yun; T E Wagner
Journal:  J Reprod Fertil       Date:  1992-05

6.  The acromegaly syndrome. Relation between clinical features, growth hormone values and radiological characteristics of the pituitary tumours.

Authors:  A Jadresic; L M Banks; D F Child; L Diamant; F H Doyle; T R Fraser; G F Joplin
Journal:  Q J Med       Date:  1982

7.  Effect of genetic background on growth of mice hemizygous for wild-type or dwarf mutated bovine growth hormone transgenes.

Authors:  E J Eisen; M Fortman; W Y Chen; J J Kopchick
Journal:  Theor Appl Genet       Date:  1993-10       Impact factor: 5.699

8.  Development of obesity following inactivation of a growth hormone transgene in mice.

Authors:  D Pomp; A M Oberbauer; J D Murray
Journal:  Transgenic Res       Date:  1996-01       Impact factor: 2.788

9.  Regulation of insulin-like growth factor-I and binding protein-3 expression in oMtla-oGH transgenic mice.

Authors:  J C Chow; J D Murray; D Pomp; R L Baldwin; C C Calvert; A M Oberbauer
Journal:  Transgenic Res       Date:  1994-03       Impact factor: 2.788

10.  Sperm from mice carrying one or two t haplotypes are deficient in investment and oocyte penetration.

Authors:  L R Johnson; S H Pilder; J L Bailey; P Olds-Clarke
Journal:  Dev Biol       Date:  1995-03       Impact factor: 3.582

View more
  2 in total

1.  Mendel: a simple excel workbook to compare the observed and expected distributions of genotypes/phenotypes in transgenic and knockout mouse crosses involving up to three unlinked loci by means of a χ2 test.

Authors:  Lluís Montoliu
Journal:  Transgenic Res       Date:  2011-08-19       Impact factor: 2.788

2.  Abnormal motor function and dopamine neurotransmission in DYT1 DeltaGAG transgenic mice.

Authors:  Yu Zhao; Michael DeCuypere; Mark S LeDoux
Journal:  Exp Neurol       Date:  2008-01-19       Impact factor: 5.330

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.