Literature DB >> 11163963

Genomic organization and alternative transcripts of the human PQBP-1 gene.

K Iwamoto1, Y Huang, S Ueda.   

Abstract

PQBP-1 has been identified as a protein that binds to huntingtin, androgen receptor and transcription factor Brain-2 through their homopolymeric glutamine repeats. We here report the genomic organization of the human PQBP-1 gene and its multiple alternative transcripts. The coding region of PQBP-1 comprises six exons and five introns, and four types of alternative transcript, designated PQBP-1a to PQBP-1d, were found in addition to the PQBP-1 transcript reported originally. All of the PQBP-1 transcripts retain the WW domain in the N-terminal region, a potent transactivator domain. On the other hand, there is a wide variation in their C-terminal regions. Importantly, PQBP-1a and PQBP-1d lack the domain responsible for the interaction with homopolymeric glutamine repeats and a nuclear localization signal.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11163963     DOI: 10.1016/s0378-1119(00)00437-6

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  2 in total

1.  The Renpenning syndrome-associated protein PQBP1 facilitates the nuclear import of splicing factor TXNL4A through the karyopherin β2 receptor.

Authors:  Xian Liu; Lin-Xia Dou; Junhai Han; Zi Chao Zhang
Journal:  J Biol Chem       Date:  2020-02-10       Impact factor: 5.157

Review 2.  Fatal Attraction: The Case of Toxic Soluble Dimers of Truncated PQBP-1 Mutants in X-Linked Intellectual Disability.

Authors:  Yu Wai Chen; Shah Kamranur Rahman
Journal:  Int J Mol Sci       Date:  2021-02-24       Impact factor: 5.923

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.