Literature DB >> 11054573

Characterization of the human tubulin tyrosine ligase-like 1 gene (TTLL1) mapping to 22q13.1.

V Trichet1, M Ruault, G Roizès, A De Sario.   

Abstract

This paper reports the characterization of the human tubulin tyrosine ligase-like 1 gene (TTLL1), which maps to the chromosome region 22q13.1 and has been partially duplicated on three other acrocentric chromosomes: 13, 15 and 21. We describe the complete cDNA, TTLL1a, coding for the putative 423 amino acid long TTLL1 and alternative transcripts coding for truncated TTLL1. Likely TTLL1a corresponds to the 1.8 kb transcript that was detected in a wide range of tissues and has a stronger expression in heart, brain and testis. A 4.8 kb transcript was found only in brain tissues. We present an interspecies sequence comparison, revealing three conserved domains, named TTLD1, TTLD2 and TTLD3, that are specific to the TTLs and TTL-like proteins.

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Year:  2000        PMID: 11054573     DOI: 10.1016/s0378-1119(00)00383-8

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


  4 in total

1.  Disruption of Ttll5/stamp gene (tubulin tyrosine ligase-like protein 5/SRC-1 and TIF2-associated modulatory protein gene) in male mice causes sperm malformation and infertility.

Authors:  Geun-Shik Lee; Yuanzheng He; Edward J Dougherty; Maria Jimenez-Movilla; Matteo Avella; Sean Grullon; David S Sharlin; Chunhua Guo; John A Blackford; Smita Awasthi; Zhenhuan Zhang; Stephen P Armstrong; Edra C London; Weiping Chen; Jurrien Dean; S Stoney Simons
Journal:  J Biol Chem       Date:  2013-04-04       Impact factor: 5.157

2.  TTLL12 expression in ovarian cancer correlates with a poor outcome.

Authors:  Shangjie Yang; Yanping Liang; Haihong Qian; Qiuhong Li
Journal:  Int J Clin Exp Pathol       Date:  2020-02-01

3.  Deep RNA sequencing reveals novel cardiac transcriptomic signatures for physiological and pathological hypertrophy.

Authors:  Hong Ki Song; Seong-Eui Hong; Taeyong Kim; Do Han Kim
Journal:  PLoS One       Date:  2012-04-16       Impact factor: 3.240

4.  Novel splice-site mutation in TTLL5 causes cone dystrophy in a consanguineous family.

Authors:  Miguel de Sousa Dias; Christian P Hamel; Isabelle Meunier; Juliette Varin; Steven Blanchard; Fiona Boyard; José-Alain Sahel; Christina Zeitz
Journal:  Mol Vis       Date:  2017-03-18       Impact factor: 2.367

  4 in total

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