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Molecular cloning and characterization of the mouse and human TUSP gene, a novel member of the tubby superfamily

  • Quan Zhen Li
    ,
  • Cong Yi Wang
    ,
  • Jin Da Shi
    ,
  • Qing Guo Ruan
    ,
  • Sarah Eckenrode
    ,
  • Abdoreza Davoodi-Semiromi
*Corresponding author for this work
  • University of Florida
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

We report here the cloning and characterization of a novel gene belonging to the tubby superfamily proteins (TUSP) in mouse and human. The mouse Tusp cDNA is 9120 bp in length and encodes a deduced protein of 1547 amino acids, while the human TUSP gene is 11,127 bp and encodes a deduced protein of 1544 amino acids. The human and mouse genes are 87% identical for their nucleotide sequences and 85% identical for their amino acid sequences. The protein sequences of these genes are 40-48% identical to other tubby family proteins at the C-terminal conserved 'tubby domain'. In addition, the TUSP proteins contain a tubby signature motif (FXGRVTQ), two bipartite nuclear localization signals (NLSs) at the C-terminal, two proline-rich regions, one WD40 repeat region and one suppressor of cytokines signaling domain. Transfection assay with green fluorescent protein-tagged TUSP expression constructs showed that the complete TUSP protein and the N-terminal portion of TUSP are localized in the cytoplasm but the C-terminal portion with the two NLSs produced distinct dots or spots localized in the cytoplasm. Northern blotting analysis showed that the major transcript with the complete coding sequence is expressed mainly in the brain, skeletal muscle, testis and kidney. Radiation hybrid mapping localized the mouse gene to chromosome 17q13 and the human TUSP gene to chromosome 6q25-q26 near the type 1 diabetes gene IDDM5. However, association analysis in diabetic families with a polymorphic microsatellite marker did not show any evidence for association between TUSP and type 1 diabetes. The precise biological function of the tubby superfamily genes is still unknown; the highly conserved tubby domain in different species, however, suggests that these proteins must have fundamental biological functions in a wide range of multi-cellular organisms.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 275-284 (10 pages)

Journal (Volume, Issue Number)

Gene (Volume 273, Issue 2)

Publication milestones

  • Published - 08/08/2001

Publication status

Published - 08/08/2001

ISSN

0378-1119

Publication IDs

  • Scopus: 0035827906
  • PubMed: 11595174

Publication metrics

Metrics

SciVal
citations
24
Fractional count
1
Fractional count
0.09
Fractional count
10
Fractional count
0.91
Fractional count
1
Fractional count
1
SciVal
FWCI
0.76
SciVal
Author count
11
SciVal
Paper percentile
73
Scopus
citations

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Citation count
25
Captures
23

Funding Details

The authors wish to thank Drs Predeep G. Kumar, Malini Laloraya and Richard McIndoe for helpful discussions. This research was supported by NIH grants P01 AI-42288 (J.-X.S.).
FundersFunding number
NIH
-
NIAID
P01AI042288