Human Molecular Genetics, Vol 8, 683-690, Copyright © 1999 by Oxford University Press
MP Lee, S Brandenburg, GM Landes, M Adams, G Miller and AP Feinberg
We previously reported the isolation of a 2.5 Mb tumor-suppressing
subchromosomal transferable fragment (STF) from human chromosome 11p15 and
the identification of nine known genes and four novel genes within this
STF. We now report the isolation of two novel cDNAs, designated here as
TSSC4 and TSSC6 (tumor-suppressing STF cDNA 4 and 6), located within the
STF. TSSC4 and TSSC6 encode predicted proteins of 329 and 290 amino acids,
respectively, with no close similarity to previously reported proteins.
TSSC4 and TSSC6 are both located in the center of a 1 Mb imprinted domain,
which contains the imprinted genes TSSC3, TSSC5, p57(KIP2), KVLQT1, ASCL2,
IGF2 and H19. However, we found that neither TSSC4 nor TSSC6 was
significantly imprinted in any of the fetal or extra-embryonic tissues
examined. Based on this result, the imprinted gene domain of 11p15 appears
to contain at least two imprinted subdomains, between which TSSC4 and TSSC6
substantially escape imprinting, due either to lack of initial silencing or
to an early developmental relaxation of imprinting.
ARTICLES
Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting
Department of Medicine, Johns Hopkins University School of Medicine, 1064 Ross, 720 Rutland Avenue, Baltimore, MD 21205, USA.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
I. Zaitoun and H. Khatib Comparative genomic imprinting and expression analysis of six cattle genes J Anim Sci, January 1, 2008; 86(1): 25 - 32. [Abstract] [Full Text] [PDF] |
||||
![]() |
A.P. FEINBERG A Genetic Approach to Cancer Epigenetics Cold Spring Harb Symp Quant Biol, January 1, 2005; 70(0): 335 - 341. [Abstract] [PDF] |
||||
![]() |
M. Paulsen, T. Khare, C. Burgard, S. Tierling, and J. Walter Evolution of the Beckwith-Wiedemann syndrome region in vertebrates Genome Res., January 1, 2005; 15(1): 146 - 153. [Abstract] [Full Text] [PDF] |
||||
![]() |
B Kerr, M L Mucchielli, S Sigaudy, M Fabre, P Saunier, M A Voelckel, E Howard, R Elles, T O B Eden, G C Black, et al. Is the locus for Costello syndrome on 11p? J. Med. Genet., June 1, 2003; 40(6): 469 - 471. [Full Text] [PDF] |
||||
![]() |
N. L. Mahy, P. E. Perry, and W. A. Bickmore Gene density and transcription influence the localization of chromatin outside of chromosome territories detectable by FISH J. Cell Biol., December 9, 2002; 159(5): 753 - 763. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Tarrant, J. Groom, D. Metcalf, R. Li, B. Borobokas, M. D. Wright, D. Tarlinton, and L. Robb The Absence of Tssc6, a Member of the Tetraspanin Superfamily, Does Not Affect Lymphoid Development but Enhances In Vitro T-Cell Proliferative Responses Mol. Cell. Biol., July 15, 2002; 22(14): 5006 - 5018. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Weksberg, J. Nishikawa, O. Caluseriu, Y.-L. Fei, C. Shuman, C. Wei, L. Steele, J. Cameron, A. Smith, I. Ambus, et al. Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1 Hum. Mol. Genet., December 1, 2001; 10(26): 2989 - 3000. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. M. John, J. F. -X. Ainscough, S. C. Barton, and M. A. Surani Distant cis-elements regulate imprinted expression of the mouse p57 Kip2 (Cdkn1c) gene: implications for the human disorder, Beckwith-Wiedemann syndrome Hum. Mol. Genet., July 1, 2001; 10(15): 1601 - 1609. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Engemann, M. Strodicke, M. Paulsen, O. Franck, R. Reinhardt, N. Lane, W. Reik, and J. Walter Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting Hum. Mol. Genet., November 1, 2000; 9(18): 2691 - 2706. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Onyango, W. Miller, J. Lehoczky, C. T. Leung, B. Birren, S. Wheelan, K. Dewar, and A. P. Feinberg Sequence and Comparative Analysis of the Mouse 1-Megabase Region Orthologous to the Human 11p15 Imprinted Domain Genome Res., November 1, 2000; 10(11): 1697 - 1710. [Abstract] [Full Text] |
||||
![]() |
W. Hartmann, A. Waha, A. Koch, C. G. Goodyer, S. Albrecht, D. von Schweinitz, and T. Pietsch p57KIP2 Is Not Mutated in Hepatoblastoma but Shows Increased Transcriptional Activity in a Comparative Analysis of the Three Imprinted Genes p57KIP2, IGF2, and H19 Am. J. Pathol., October 1, 2000; 157(4): 1393 - 1403. [Abstract] [Full Text] [PDF] |
||||
![]() |
S.-i. Horike, K. Mitsuya, M. Meguro, N. Kotobuki, A. Kashiwagi, T. Notsu, T. C. Schulz, Y. Shirayoshi, and M. Oshimura Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome Hum. Mol. Genet., September 1, 2000; 9(14): 2075 - 2083. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Paulsen, O. El-Maarri, S. Engemann, M. Strodicke, O. Franck, K. Davies, R. Reinhardt, W. Reik, and J. Walter Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse Hum. Mol. Genet., July 22, 2000; 9(12): 1829 - 1841. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Prawitt, T. Enklaar, G. Klemm, B. Gartner, C. Spangenberg, A. Winterpacht, M. Higgins, J. Pelletier, and B. Zabel Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression Hum. Mol. Genet., January 22, 2000; 9(2): 203 - 216. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Mitsuya, M. Meguro, M. P. Lee, M. Katoh, T. C. Schulz, H. Kugoh, M. A. Yoshida, N. Niikawa, A. P. Feinberg, and M. Oshimura LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids Hum. Mol. Genet., July 1, 1999; 8(7): 1209 - 1217. [Abstract] [Full Text] [PDF] |
||||







