The novel gene, γ2-COP (COPG2), in the 7q32 imprinted domain escapes genomic imprinting

被引:30
作者
Yamasaki, K
Hayashida, S
Miura, K
Masuzaki, H
Ishimaru, T
Niikawa, N
Kishino, T
机构
[1] Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
[2] Nagasaki Univ, Sch Med, Dept Obstet & Gynecol, Nagasaki 8528523, Japan
关键词
D O I
10.1006/geno.2000.6265
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The gene MEST (or PEG1) on chromosome 7q32 is paternally expressed in human fetal tissues as a result of genomic imprinting. Since some imprinted genes are clustered, we speculated that an imprinted gene cluster might exist at 7q32. We have sought to isolate additional human genes close to MEST and to characterize their allelic expression patterns. Here, we report the biallelic expression of the gene, gamma 2-COP (coatomer protein complex, subunit gamma 2, HUGO-approved symbol COPG2), and monoallelic expression of the transcript, CIT1, which is located in intron 20 of gamma 2-COP. Recently, gamma 2-COP was reported to be a novel imprinted gene that overlaps the 3'-untranslated region (3'-UTR) of MEST in a tail-to-tail orientation. However, our results revealed biallelic expression in all fetal tissues and adult blood lymphocytes. On the other hand, CIT1 was an antisense transcript of gamma 2-COP intron 20 and was expressed from the paternal allele in all fetal tissues examined. Adult blood lymphocytes showed biallelic expression. We identified additional MEST 3'-UTR sequence, which overlaps the last four exons and introns of gamma 2-COP. This additional MEST 3'-UTR may complicate analysis of gamma 2-COP imprinting. Our data indicate that the region containing MEST at 7q32 is an imprinted domain, but gamma 2-COP adjacent to MEST escapes genomic imprinting. (C) 2000 Academic Press.
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页码:330 / 335
页数:6
相关论文
共 20 条
[11]   Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene [J].
Miyoshi, N ;
Kuroiwa, Y ;
Kohda, T ;
Shitara, H ;
Yonekawa, H ;
Kawabe, T ;
Hasegawa, H ;
Barton, SC ;
Surani, MA ;
Kaneko-Ishino, T ;
Ishino, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (03) :1102-1107
[12]   GENOMIC IMPRINTING IN MAMMALIAN DEVELOPMENT - A PARENTAL TUG-OF-WAR [J].
MOORE, T ;
HAIG, D .
TRENDS IN GENETICS, 1991, 7 (02) :45-49
[13]   A catalogue of imprinted genes and parent-of-origin effects in humans and animals [J].
Morison, IM ;
Reeve, AE .
HUMAN MOLECULAR GENETICS, 1998, 7 (10) :1599-1609
[14]   RELAXATION OF IMPRINTED GENES IN HUMAN CANCER [J].
RAINIER, S ;
JOHNSON, LA ;
DOBRY, CJ ;
PING, AJ ;
GRUNDY, PE ;
FEINBERG, AP .
NATURE, 1993, 362 (6422) :747-749
[15]   Imprinting in clusters: Lessons from Beckwith-Wiedemann syndrome [J].
Reik, W ;
Maher, ER .
TRENDS IN GENETICS, 1997, 13 (08) :330-334
[16]   Evidence against a major role of PEG1/MEST in Silver-Russell syndrome [J].
Riesewijk, AM ;
Blagitko, N ;
Schinzel, AA ;
Hu, LD ;
Schulz, U ;
Hamel, BCJ ;
Ropers, HH ;
Kalscheuer, VM .
EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 (02) :114-120
[17]   DELETIONS OF A DIFFERENTIALLY METHYLATED CPG ISLAND AT THE SNRPN GENE DEFINE A PUTATIVE IMPRINTING CONTROL REGION [J].
SUTCLIFFE, JS ;
NAKAO, M ;
CHRISTIAN, S ;
ORSTAVIK, KH ;
TOMMERUP, N ;
LEDBETTER, DH ;
BEAUDET, AL .
NATURE GENETICS, 1994, 8 (01) :52-58
[18]   The sins of the fathers and mothers: Genomic imprinting in mammalian development [J].
Tilghman, SM .
CELL, 1999, 96 (02) :185-193
[19]   Imprinted expression of the Igf2r gene depends on an intronic CpG island [J].
Wutz, A ;
Smrzka, OW ;
Schweifer, N ;
Schellander, K ;
Wagner, EF ;
Barlow, DP .
NATURE, 1997, 389 (6652) :745-749
[20]   Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome [J].
Yoshihashi, H ;
Maeyama, K ;
Kosaki, R ;
Ogata, T ;
Tsukahara, M ;
Goto, Y ;
Hata, J ;
Matsuo, N ;
Smith, RJ ;
Kosaki, K .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (02) :476-482