Literature DB >> 14962666

Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q32.

Takahiro Yamada1, Kohzoh Mitsuya, Tomohiko Kayashima, Kentaro Yamasaki, Tohru Ohta, Koh-ichiro Yoshiura, Naomichi Matsumoto, Hideto Yamada, Hisanori Minakami, Mitsuo Oshimura, Norio Niikawa, Tatsuya Kishino.   

Abstract

MEST is one of the imprinted genes in human. With the assistance of our integration map and the complete sequence in the registry, we mapped a total of 16 genes/transcripts at the 1.5-Mb MEST-flanking region at 7q32. This region has been suggested to form an imprinted gene cluster, because MEST and its three flanking genes/transcripts (MESTIT1, CPA4, and COPG2IT1) were reported to be imprinted, although two (TSGA14 and COPG2) were shown to escape imprinting. In this study, 10 other genes/transcripts were examined for their imprinting status in human fetal tissues. The results indicated that 8 genes/transcripts (NRF1, UBE2H, HSPC216, KIAA0265, FLJ14803, CPA2, CPA1, and DKFZp667F0312) were expressed biallelically. The imprinting status of two (TSGA13 and CPA5) was not conclusive, because of their weak and/or tissue-specific expression and inconstant results. These findings provided evidence that only 4 of the 16 genes/transcripts located to the region show monoallelic expression, while others are not involved in imprinting. Therefore, it is less likely that the MEST-flanking 7q32 region forms a large imprinted domain.

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Year:  2004        PMID: 14962666     DOI: 10.1016/j.ygeno.2003.08.016

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  5 in total

1.  Dynamic expression patterns of imprinted genes in human embryonic stem cells following prolonged passaging and differentiation.

Authors:  Xiuyun Mai; Qingyun Mai; Tao Li; Canquan Zhou
Journal:  J Assist Reprod Genet       Date:  2010-12-16       Impact factor: 3.412

2.  Loss of inherited genomic imprints in mice leads to severe disruption in placental lipid metabolism.

Authors:  K P Himes; A Young; E Koppes; D Stolz; Y Barak; Y Sadovsky; J R Chaillet
Journal:  Placenta       Date:  2015-01-29       Impact factor: 3.481

3.  Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells.

Authors:  Masayuki Haruta; Makiko Meguro; Yu-Ki Sakamoto; Hidetoshi Hoshiya; Akiko Kashiwagi; Yasuhiko Kaneko; Kohzoh Mitsuya; Mitsuo Oshimura
Journal:  J Hum Genet       Date:  2005-03-03       Impact factor: 3.172

4.  Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

Authors:  J A Lamb; G Barnby; E Bonora; N Sykes; E Bacchelli; F Blasi; E Maestrini; J Broxholme; J Tzenova; D Weeks; A J Bailey; A P Monaco
Journal:  J Med Genet       Date:  2005-02       Impact factor: 6.318

5.  Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution.

Authors:  Layla Parker-Katiraee; Andrew R Carson; Takahiro Yamada; Philippe Arnaud; Robert Feil; Sayeda N Abu-Amero; Gudrun E Moore; Masahiro Kaneda; George H Perry; Anne C Stone; Charles Lee; Makiko Meguro-Horike; Hiroyuki Sasaki; Keiko Kobayashi; Kazuhiko Nakabayashi; Stephen W Scherer
Journal:  PLoS Genet       Date:  2007-03-12       Impact factor: 5.917

  5 in total

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