Literature DB >> 11543638

The neuronatin gene resides in a "micro-imprinted" domain on human chromosome 20q11.2.

H K Evans1, A A Wylie, S K Murphy, R L Jirtle.   

Abstract

A small fraction of the genome contains genes that are imprinted and thus expressed exclusively from one parental allele. We report here that the human neuronatin gene (NNAT) on chromosome 20q11.2 is imprinted and transcribed specifically from the paternal allele. The region containing NNAT has multiple CpG islands, and methylation analysis showed that a 1.8-kb CpG island in its promoter region exhibits differential methylation in all tissues examined. This finding is consistent with the island acting as a component of the NNAT imprint control domain. NNAT lies within the singular 8.5-kb intron of the gene encoding bladder cancer-associated protein (BLCAP), which, as we demonstrate, is not imprinted. This study provides the first example, to our knowledge, in humans of an imprinted gene contained within the genomic structure of a nonimprinted gene. Thus, NNAT is in an imprinted "microdomain," making this locus uniquely suited for the investigation of mechanisms of localized imprint regulation.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11543638     DOI: 10.1006/geno.2001.6612

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


  32 in total

1.  Identification of novel imprinted genes in a genome-wide screen for maternal methylation.

Authors:  Rachel J Smith; Wendy Dean; Galia Konfortova; Gavin Kelsey
Journal:  Genome Res       Date:  2003-04       Impact factor: 9.043

2.  High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes.

Authors:  Elena Allen; Steve Horvath; Frances Tong; Peter Kraft; Elizabeth Spiteri; Arthur D Riggs; York Marahrens
Journal:  Proc Natl Acad Sci U S A       Date:  2003-08-08       Impact factor: 11.205

3.  Characterization of global loss of imprinting in fetal overgrowth syndrome induced by assisted reproduction.

Authors:  Zhiyuan Chen; Darren E Hagen; Christine G Elsik; Tieming Ji; Collin James Morris; Laura Emily Moon; Rocío Melissa Rivera
Journal:  Proc Natl Acad Sci U S A       Date:  2015-03-30       Impact factor: 11.205

Review 4.  The role of imprinted genes in fetal growth abnormalities.

Authors:  Jorge A Piedrahita
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2011-06-06

5.  Genome-wide prediction of imprinted murine genes.

Authors:  Philippe P Luedi; Alexander J Hartemink; Randy L Jirtle
Journal:  Genome Res       Date:  2005-06       Impact factor: 9.043

Review 6.  The human imprintome: regulatory mechanisms, methods of ascertainment, and roles in disease susceptibility.

Authors:  David A Skaar; Yue Li; Autumn J Bernal; Cathrine Hoyo; Susan K Murphy; Randy L Jirtle
Journal:  ILAR J       Date:  2012

7.  Clinical and genetic characterization of Portuguese patients with pseudohypoparathyroidism type Ib.

Authors:  Branca Maria Cavaco; Rute Alexandra Tomaz; Fernando Fonseca; Mário Rui Mascarenhas; Valeriano Leite; Luís Gonçalves Sobrinho
Journal:  Endocrine       Date:  2010-03-30       Impact factor: 3.633

8.  Altered neuronatin expression in the rat dorsal root ganglion after sciatic nerve transection.

Authors:  Kuan-Hung Chen; Chien-Hui Yang; Jiin-Tsuey Cheng; Chih-Hsien Wu; Wei-Dih Sy; Chung-Ren Lin
Journal:  J Biomed Sci       Date:  2010-05-28       Impact factor: 8.410

9.  Coexpression of neuronatin splice forms promotes medulloblastoma growth.

Authors:  I-Mei Siu; Renyuan Bai; Gary L Gallia; Jennifer B Edwards; Betty M Tyler; Charles G Eberhart; Gregory J Riggins
Journal:  Neuro Oncol       Date:  2008-08-13       Impact factor: 12.300

10.  Unwitting hosts fall victim to imprinting.

Authors:  Ruth B McCole; Rebecca J Oakey
Journal:  Epigenetics       Date:  2008-09-19       Impact factor: 4.528

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.