Literature DB >> 26485282

Poreless eggshells.

Haifan Lin, Martin M Matzuk.   

Abstract

The oocyte is the sole source of the female genetic material that will be fertilized by sperm to form an embryo. Many extrinsic and intrinsic factors are critical for oocyte development and survival; however, these mediators are incompletely understood. In this issue of the JCI, Weinberg-Shukron et al. uncover a novel recessive missense mutation in the gene encoding nucleoporin-107 (NUP107) that results in abnormal ovarian development. Recapitulation of the human mutation in the Drosophila NUP107 ortholog resulted in poor follicular development and demonstrated an evolutionarily conserved and ovary-specific role of NUP107. While NUP107 is required for nuclear pore complex function in somatic cells of flies and women, this specific amino acid change appears only to be disruptive in the ovary. All together, these findings imply that missense mutations in other genes could be specifically disruptive of ovarian or testicular function, while leaving extragonadal function intact.

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Year:  2015        PMID: 26485282      PMCID: PMC4639988          DOI: 10.1172/JCI84692

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  13 in total

Review 1.  Asymmetric germ cell division and oocyte determination during Drosophila oogenesis.

Authors:  W Deng; H Lin
Journal:  Int Rev Cytol       Date:  2001

2.  The mammalian oocyte orchestrates the rate of ovarian follicular development.

Authors:  John J Eppig; Karen Wigglesworth; Frank L Pendola
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-26       Impact factor: 11.205

Review 3.  Intercellular communication in the mammalian ovary: oocytes carry the conversation.

Authors:  Martin M Matzuk; Kathleen H Burns; Maria M Viveiros; John J Eppig
Journal:  Science       Date:  2002-06-21       Impact factor: 47.728

Review 4.  The mammalian ovary from genesis to revelation.

Authors:  Mark A Edson; Ankur K Nagaraja; Martin M Matzuk
Journal:  Endocr Rev       Date:  2009-09-23       Impact factor: 19.871

5.  A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis.

Authors:  Ariella Weinberg-Shukron; Paul Renbaum; Rachel Kalifa; Sharon Zeligson; Ziva Ben-Neriah; Amatzia Dreifuss; Amal Abu-Rayyan; Noa Maatuk; Nilly Fardian; Dina Rekler; Moien Kanaan; Abraham O Samson; Ephrat Levy-Lahad; Offer Gerlitz; David Zangen
Journal:  J Clin Invest       Date:  2015-10-20       Impact factor: 14.808

Review 6.  Reproductive tract function and dysfunction in women.

Authors:  Angshumoy Roy; Martin M Matzuk
Journal:  Nat Rev Endocrinol       Date:  2011-05-24       Impact factor: 43.330

7.  Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.

Authors:  Lina Basel-Vanagaite; Liora Muncher; Rachel Straussberg; Metsada Pasmanik-Chor; Michal Yahav; Limor Rainshtein; Christopher A Walsh; Nurit Magal; Ellen Taub; Valerie Drasinover; Hanna Shalev; Revital Attia; Gideon Rechavi; Amos J Simon; Mordechai Shohat
Journal:  Ann Neurol       Date:  2006-08       Impact factor: 10.422

8.  The nucleoporin Seh1 forms a complex with Mio and serves an essential tissue-specific function in Drosophila oogenesis.

Authors:  Stefania Senger; John Csokmay; Tanveer Akbar; Akbar Tanveer; Takako Iida Jones; Prabuddha Sengupta; Mary A Lilly
Journal:  Development       Date:  2011-05       Impact factor: 6.868

9.  Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death.

Authors:  Xianqin Zhang; Shenghan Chen; Shin Yoo; Susmita Chakrabarti; Teng Zhang; Tie Ke; Carlos Oberti; Sandro L Yong; Fang Fang; Lin Li; Roberto de la Fuente; Lejin Wang; Qiuyun Chen; Qing Kenneth Wang
Journal:  Cell       Date:  2008-12-12       Impact factor: 41.582

10.  A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility.

Authors:  S Bione; C Sala; C Manzini; G Arrigo; O Zuffardi; S Banfi; G Borsani; P Jonveaux; C Philippe; M Zuccotti; A Ballabio; D Toniolo
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

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