Mammalian Genetics Unit, MRC Harwell, Harwell Science and Innovation Campus, Oxfordshire, OX11 0RD, UK.
Mamm Genome. 2013 Aug;24(7-8):276-85. doi: 10.1007/s00335-013-9462-2. Epub 2013 Jul 10.
Genes subjected to genomic imprinting are often associated with prenatal and postnatal growth. Furthermore, it has been observed that maternally silenced/paternally expressed genes tend to favour offspring growth, whilst paternally silenced/maternally expressed genes will restrict growth. One imprinted cluster in which this has been shown to hold true is the Gnas cluster; of the three proteins expressed from this cluster, two, Gsα and XLαs, have been found to affect postnatal growth in a number of different mouse models. The remaining protein in this cluster, NESP55, has not yet been shown to be involved in growth. We previously described a new mutation, Ex1A-T, which upon paternal transmission resulted in postnatal growth retardation due to loss of imprinting of Gsα and loss of expression of the paternally expressed XLαs. Here we describe maternal inheritance of Ex1A-T which gives rise to a small but highly significant overgrowth phenotype which we attribute to reduction of maternally expressed NESP55.
受基因组印记调控的基因通常与产前和产后生长有关。此外,人们观察到,母源沉默/父源表达的基因往往有利于后代的生长,而父源沉默/母源表达的基因则会限制生长。在一个被证明符合这一规律的印记簇中,Gnas 簇就是其中之一;在这个簇中表达的三种蛋白质中,已经发现有两种,Gsα 和 XLαs,在许多不同的小鼠模型中影响产后生长。这个簇中的剩余蛋白 NESP55 尚未被证明参与生长。我们之前描述了一种新的突变 Ex1A-T,当它通过父系传递时,由于 Gsα 的印记丢失和父系表达的 XLαs 的表达丢失,导致产后生长迟缓。在这里,我们描述了 Ex1A-T 的母系遗传,它导致了一个小但非常显著的过度生长表型,我们将其归因于母系表达的 NESP55 的减少。