Literature DB >> 10775177

Identification of a novel testis-specific leucine-rich protein in humans and mice.

J C Xue1, E Goldberg.   

Abstract

A novel testis-specific protein, termed LRTP, was identified by screening both human and mouse testis and mouse pachytene spermatocyte cDNA libraries. Sequence analyses (GenBank accession number: AF092208) revealed that LRTP contains an amino terminus leucine-rich repeat domain. There are several acidic regions rich in glutamic acid in the C-terminus. The sequence, by GenBank search, shows similarities to LANP and SDS22+, leucine-rich repeat proteins localized to the nucleus and involved in the regulation of protein phosphatases. In mouse, the mRNA is first detected at about Day 14 postpartum, presumably when mid-pachytene spermatocytes are first seen. In situ hybridization confirmed the expression of the LRTP mRNA at this stage of spermatogenesis. Immunohistochemical analysis revealed that the protein is most abundant in the cytoplasm of pachytene and diplotene cells, corresponding to late prophase of meiosis I. Immunohistochemical localization is markedly reduced in secondary spermatocytes, suggesting a functional association of LRTP with meiosis. An LRTP cDNA probe did not bind to mouse ovary RNA in a dot blot assay.

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Year:  2000        PMID: 10775177     DOI: 10.1095/biolreprod62.5.1278

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  12 in total

1.  Identification of a novel leucine-rich repeat protein as a component of flagellar radial spoke in the Ascidian Ciona intestinalis.

Authors:  Potturi Padma; Yuhkoh Satouh; Ken-Ichi Wakabayashi; Akiko Hozumi; Yuji Ushimaru; Ritsu Kamiya; Kazuo Inaba
Journal:  Mol Biol Cell       Date:  2003-02       Impact factor: 4.138

2.  An evolutionarily conserved coiled-coil protein implicated in polycystic kidney disease is involved in basal body duplication and flagellar biogenesis in Trypanosoma brucei.

Authors:  Gareth W Morgan; Paul W Denny; Sue Vaughan; David Goulding; Tim R Jeffries; Deborah F Smith; Keith Gull; Mark C Field
Journal:  Mol Cell Biol       Date:  2005-05       Impact factor: 4.272

3.  Hearing in Drosophila requires TilB, a conserved protein associated with ciliary motility.

Authors:  Ryan G Kavlie; Maurice J Kernan; Daniel F Eberl
Journal:  Genetics       Date:  2010-03-09       Impact factor: 4.562

4.  Molecular determinants of NOTCH4 transcription in vascular endothelium.

Authors:  Jing Wu; Fumiko Iwata; Jeffrey A Grass; Cameron S Osborne; Laura Elnitski; Peter Fraser; Osamu Ohneda; Masayuki Yamamoto; Emery H Bresnick
Journal:  Mol Cell Biol       Date:  2005-02       Impact factor: 4.272

5.  Mutations in zebrafish leucine-rich repeat-containing six-like affect cilia motility and result in pronephric cysts, but have variable effects on left-right patterning.

Authors:  Fabrizio C Serluca; Bo Xu; Noriko Okabe; Kari Baker; Shin-Yi Lin; Jessica Sullivan-Brown; David J Konieczkowski; Kimberly M Jaffe; Joshua M Bradner; Mark C Fishman; Rebecca D Burdine
Journal:  Development       Date:  2009-05       Impact factor: 6.868

6.  Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia.

Authors:  Esther Kott; Philippe Duquesnoy; Bruno Copin; Marie Legendre; Florence Dastot-Le Moal; Guy Montantin; Ludovic Jeanson; Aline Tamalet; Jean-François Papon; Jean-Pierre Siffroi; Nathalie Rives; Valérie Mitchell; Jacques de Blic; André Coste; Annick Clement; Denise Escalier; Aminata Touré; Estelle Escudier; Serge Amselem
Journal:  Am J Hum Genet       Date:  2012-11-02       Impact factor: 11.025

Review 7.  Genetic factors contributing to human primary ciliary dyskinesia and male infertility.

Authors:  Zhi-Yong Ji; Yan-Wei Sha; Lu Ding; Ping Li
Journal:  Asian J Androl       Date:  2017 Sep-Oct       Impact factor: 3.285

8.  Whole-Exome Sequencing Identified a Novel Compound Heterozygous Mutation of LRRC6 in a Chinese Primary Ciliary Dyskinesia Patient.

Authors:  Lv Liu; Hong Luo
Journal:  Biomed Res Int       Date:  2018-01-08       Impact factor: 3.411

9.  Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility.

Authors:  Isabella Aprea; Johanna Raidt; Inga Marlena Höben; Niki Tomas Loges; Tabea Nöthe-Menchen; Petra Pennekamp; Heike Olbrich; Thomas Kaiser; Luisa Biebach; Frank Tüttelmann; Judit Horvath; Maria Schubert; Claudia Krallmann; Sabine Kliesch; Heymut Omran
Journal:  PLoS Genet       Date:  2021-02-26       Impact factor: 5.917

10.  LRRC6 mutation causes primary ciliary dyskinesia with dynein arm defects.

Authors:  Amjad Horani; Thomas W Ferkol; David Shoseyov; Mollie G Wasserman; Yifat S Oren; Batsheva Kerem; Israel Amirav; Malena Cohen-Cymberknoh; Susan K Dutcher; Steven L Brody; Orly Elpeleg; Eitan Kerem
Journal:  PLoS One       Date:  2013-03-19       Impact factor: 3.240

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