Literature DB >> 15383328

Human DDX3Y, the Y-encoded isoform of RNA helicase DDX3, rescues a hamster temperature-sensitive ET24 mutant cell line with a DDX3X mutation.

Takeshi Sekiguchi1, Hiroshi Iida, Junko Fukumura, Takeharu Nishimoto.   

Abstract

We investigated the function of DDX3Y, the Y chromosome AZFa region encoding a putative DEAD-box RNA helicase protein, the loss of which results in oligozoospermia or azoospermia in humans. The human DDX3Y amino acid sequence is similar to that of the X chromosome gene DDX3X (91.7% homology). Here we report that human Y- and X-encoded DEAD box RNA helicase proteins DDX3Y and DDX3X are interchangeable and have an essential function: both proteins rescued a temperature-sensitive mutant hamster cell line (tsET24) that was otherwise incapable of growth at a nonpermissive temperature. Mouse homologues Ddx3y and D1Pas1-PL10 also rescued the mutant cell line at a nonpermissive temperature. In situ hybridization revealed that Ddx3x mRNA was expressed in almost every cell in mouse testis, suggesting that Ddx3x is involved in spermatogenesis. A comparative study of DDX3X and DDX3Y was performed to determine the significance of DDX3Y for cell growth and spermatogenesis. Both DDX3X and DDX3Y promoter DNAs produced a similar degree of transcription in vivo, whereas deletion studies of the promoter DNAs indicated that these genes are differentially regulated. DDX3Y, similar to DDX3X, shuttles between the nucleus and cytoplasm in a crm1-dependent manner.

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Year:  2004        PMID: 15383328     DOI: 10.1016/j.yexcr.2004.07.005

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  33 in total

1.  Strong purifying selection at genes escaping X chromosome inactivation.

Authors:  Chungoo Park; Laura Carrel; Kateryna D Makova
Journal:  Mol Biol Evol       Date:  2010-06-09       Impact factor: 16.240

2.  Identification and characterization of essential genes in the human genome.

Authors:  Tim Wang; Kıvanç Birsoy; Nicholas W Hughes; Kevin M Krupczak; Yorick Post; Jenny J Wei; Eric S Lander; David M Sabatini
Journal:  Science       Date:  2015-10-15       Impact factor: 47.728

3.  Proteomic analysis of human hepatoma cells expressing methionine adenosyltransferase I/III: Characterization of DDX3X as a target of S-adenosylmethionine.

Authors:  Paul C Schröder; Joaquín Fernández-Irigoyen; Emilie Bigaud; Antonio Serna; Rubén Renández-Alcoceba; Shelly C Lu; José M Mato; Jesús Prieto; Fernando J Corrales
Journal:  J Proteomics       Date:  2012-01-16       Impact factor: 4.044

4.  The ATP-Dependent RNA Helicase DDX3X Modulates Herpes Simplex Virus 1 Gene Expression.

Authors:  Bita Khadivjam; Camille Stegen; Marc-Aurèle Hogue-Racine; Nabil El Bilali; Katinka Döhner; Beate Sodeik; Roger Lippé
Journal:  J Virol       Date:  2017-03-29       Impact factor: 5.103

5.  Translational regulation of HIV-1 replication by HIV-1 Rev cellular cofactors Sam68, eIF5A, hRIP, and DDX3.

Authors:  Jinfeng Liu; Jorge Henao-Mejia; Hao Liu; Yingren Zhao; Johnny J He
Journal:  J Neuroimmune Pharmacol       Date:  2011-03-01       Impact factor: 4.147

6.  The role of DDX3 in regulating Snail.

Authors:  Mianen Sun; Ling Song; Tong Zhou; G Yancey Gillespie; Richard S Jope
Journal:  Biochim Biophys Acta       Date:  2011-01-12

7.  Molecular analysis of TBL1Y, a Y-linked homologue of TBL1X related with X-linked late-onset sensorineural deafness.

Authors:  Hong-Tao Yan; Toshikatsu Shinka; Keigo Kinoshita; Youichi Sato; Mayumi Umeno; Gang Chen; Keiko Tsuji; Yukiko Unemi; Xin-Jun Yang; Teruaki Iwamoto; Yutaka Nakahori
Journal:  J Hum Genet       Date:  2005-04-15       Impact factor: 3.172

8.  DDX3 regulates DNA damage-induced apoptosis and p53 stabilization.

Authors:  Mianen Sun; Tong Zhou; Eric Jonasch; Richard S Jope
Journal:  Biochim Biophys Acta       Date:  2013-03-05

9.  The DEAD-box RNA helicase DDX3 associates with export messenger ribonucleoproteins as well as tip-associated protein and participates in translational control.

Authors:  Ming-Chih Lai; Yan-Hwa Wu Lee; Woan-Yuh Tarn
Journal:  Mol Biol Cell       Date:  2008-07-02       Impact factor: 4.138

10.  Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Authors:  Lot Snijders Blok; Erik Madsen; Jane Juusola; Christian Gilissen; Diana Baralle; Margot R F Reijnders; Hanka Venselaar; Céline Helsmoortel; Megan T Cho; Alexander Hoischen; Lisenka E L M Vissers; Tom S Koemans; Willemijn Wissink-Lindhout; Evan E Eichler; Corrado Romano; Hilde Van Esch; Connie Stumpel; Maaike Vreeburg; Eric Smeets; Karin Oberndorff; Bregje W M van Bon; Marie Shaw; Jozef Gecz; Eric Haan; Melanie Bienek; Corinna Jensen; Bart L Loeys; Anke Van Dijck; A Micheil Innes; Hilary Racher; Sascha Vermeer; Nataliya Di Donato; Andreas Rump; Katrina Tatton-Brown; Michael J Parker; Alex Henderson; Sally A Lynch; Alan Fryer; Alison Ross; Pradeep Vasudevan; Usha Kini; Ruth Newbury-Ecob; Kate Chandler; Alison Male; Sybe Dijkstra; Jolanda Schieving; Jacques Giltay; Koen L I van Gassen; Janneke Schuurs-Hoeijmakers; Perciliz L Tan; Igor Pediaditakis; Stefan A Haas; Kyle Retterer; Patrick Reed; Kristin G Monaghan; Eden Haverfield; Marvin Natowicz; Angela Myers; Michael C Kruer; Quinn Stein; Kevin A Strauss; Karlla W Brigatti; Katherine Keating; Barbara K Burton; Katherine H Kim; Joel Charrow; Jennifer Norman; Audrey Foster-Barber; Antonie D Kline; Amy Kimball; Elaine Zackai; Margaret Harr; Joyce Fox; Julie McLaughlin; Kristin Lindstrom; Katrina M Haude; Kees van Roozendaal; Han Brunner; Wendy K Chung; R Frank Kooy; Rolph Pfundt; Vera Kalscheuer; Sarju G Mehta; Nicholas Katsanis; Tjitske Kleefstra
Journal:  Am J Hum Genet       Date:  2015-07-30       Impact factor: 11.025

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