Literature DB >> 15305064

A reassessment of imprinting regions and phenotypes on mouse chromosome 6: Nap1l5 locates within the currently defined sub-proximal imprinting region.

C V Beechey1.   

Abstract

Previous studies (Beechey, 2000) have shown that mouse proximal chromosome (Chr) 6 has two imprinting regions. An early embryonic lethality is associated with two maternal copies of the more proximal imprinting region, while mice with two maternal copies of the sub-proximal imprinting region are growth retarded at birth, the weight reduction remaining similar to adulthood. No detectable postnatal imprinting phenotype was seen in these earlier studies with two paternal copies of either region. The sub-proximal imprinting region locates distal to the T77H reciprocal translocation breakpoint in G-band 6A3.2 and results reported here show that it does not extend beyond the breakpoint of the more distal T6Ad translocation in 6C2. It has been confirmed that the postnatal growth retardation observed with two maternal copies of the sub-proximal region is established in utero, although placental size was normal. A new finding is that 16.5-18.5-dpc embryos, with two paternal copies of the sub-proximal imprinting region, were larger than their normal sibs, although placental size was normal. As no postnatal growth differences have been observed in these mice, the fetal overgrowth must normalize by birth. The imprinted genes Peg1/Mest, Copg2, Copg2as and Mit1/Lb9 map to the sub-proximal imprinting region and are thus candidates for the observed imprinting phenotypes. Another candidate is the recently reported imprinted gene Nap1l5. Expression studies of Nap1l5 in mice with two maternal or two paternal copies of different regions of Chr 6 have demonstrated that the gene locates within the sub-proximal imprinting region. FISH has mapped Nap1l5 to G-band 6C1, within the sub-proximal imprinting region but several G-bands distal to the Peg1/Mest cluster. This location, and the 30-Mb separation of these loci on the sequence map, makes it probable that Nap1l5 defines a new imprinting domain within the currently defined sub-proximal imprinting region. Copyright 2004 S. Karger AG, Basel

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Year:  2004        PMID: 15305064     DOI: 10.1159/000079579

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


  4 in total

1.  Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia.

Authors:  Saori Aoki; Ken Higashimoto; Hidenori Hidaka; Yasufumi Ohtsuka; Shigehisa Aoki; Hiroyuki Mishima; Koh-Ichiro Yoshiura; Kazuhiko Nakabayashi; Kenichiro Hata; Hitomi Yatsuki; Satoshi Hara; Takashi Ohba; Hidetaka Katabuchi; Hidenobu Soejima
Journal:  Clin Epigenetics       Date:  2022-05-17       Impact factor: 7.259

2.  Large copy-number variations are enriched in cases with moderate to extreme obesity.

Authors:  Kai Wang; Wei-Dong Li; Joseph T Glessner; Struan F A Grant; Hakon Hakonarson; R Arlen Price
Journal:  Diabetes       Date:  2010-07-09       Impact factor: 9.461

3.  Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2.

Authors:  Julia L MacIsaac; Aaron B Bogutz; A Sorana Morrissy; Louis Lefebvre
Journal:  Nucleic Acids Res       Date:  2011-11-03       Impact factor: 16.971

4.  Genetic architecture of early pre-inflammatory stage transcription signatures of autoimmune diabetes in the pancreatic lymph nodes of the NOD mouse reveals significant gene enrichment on chromosomes 6 and 7.

Authors:  Beatrice Regnault; Evie Melanitou
Journal:  Meta Gene       Date:  2015-10-22
  4 in total

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