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NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma

*Corresponding author for this work
  • Cleveland Clinic Foundation
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Molecular cloning of the breakpoints of a t(1;10)(p22q21) constitutional translocation breakpoint in a patient with stage 4S neuroblastoma has identified two genes which are fused in-frame to generate a novel gene. The 1p22 gene, which we have called NB4S, encodes a 7.5 kb transcript with an 810 amino acid open reading frame and is expressed in a wide variety of tissues. NB4S has > 88% homology with the mouse EVI-5 gene within the coding region and shows strong homology over a 200 amino acid region with TBC1 box motif genes involved in cell growth and differentiation. The C-teminal end of the protein contains a number of coiled coil domains, indicating a possible protein-protein binding function. The chromosome 10 breakpoint interrupts a novel transcript (TRNG10) which could only be detected in tumor cells. This transcript has no exon/intron structure or significant open reading frame, suggesting that it is a structural RNA which is transcribed but not translated. The chromosome rearrangement creates a fusion gene product which combines the TBC1 motif of NB4S with a polyadenylation signal from TRNG10, potentially generating a truncated protein with oncogenic properties.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1169-1178 (10 pages)

Journal (Volume, Issue Number)

Human Molecular Genetics (Volume 7, Issue 7)

Publication milestones

  • Published - 07/1998

Publication status

Published - 07/1998

ISSN

0964-6906

Publication IDs

  • Scopus: 0031777019
  • PubMed: 9618176

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
0.97
SciVal
Author count
3
SciVal
citations
49
SciVal
Paper percentile
86
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Captures
15
Citation count
49
Mentions
2

Funding Details

We are grateful to the CCF core sequencing facility for their assistance. This work was supported by NIH grant RO1 NS35791 and the Rose-Ella Burkhardt Endowment Fund.
FundersFunding number
Rose-Ella Burkhardt Endowment Fund
-
NIH
-
NINDS
R01NS035791