Literature DB >> 11139280

Eggs to die for: cell death during Drosophila oogenesis.

M Buszczak1, L Cooley.   

Abstract

Extensive programmed cell death occurs in the female germline of many species ranging from C. elegans to humans. One purpose for germline apoptosis is to remove defective cells unable to develop into fertile eggs. In addition, recent work suggests that the death of specific germline cells may also play a vital role by providing essential nutrients to the surviving oocytes. In Drosophila, the genetic control of germline apoptosis and the proteins that carry out the death sentences are beginning to emerge from studies of female sterile mutations. These studies suggest that the morphological changes that occur during the late stages of Drosophila oogenesis may be initiated and driven by a modified form of programmed cell death.

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Year:  2000        PMID: 11139280     DOI: 10.1038/sj.cdd.4400755

Source DB:  PubMed          Journal:  Cell Death Differ        ISSN: 1350-9047            Impact factor:   15.828


  33 in total

Review 1.  Is the mitochondrial cloud the selection machinery for preferentially transmitting wild-type mtDNA between generations? Rewinding Müller's ratchet efficiently.

Authors:  Rong Rong Zhou; Bing Wang; Jing Wang; Heide Schatten; Yong Zhong Zhang
Journal:  Curr Genet       Date:  2010-02-24       Impact factor: 3.886

2.  Quantitative proteomics reveals the dynamics of protein changes during Drosophila oocyte maturation and the oocyte-to-embryo transition.

Authors:  Iva Kronja; Zachary J Whitfield; Bingbing Yuan; Kristina Dzeyk; Joanna Kirkpatrick; Jeroen Krijgsveld; Terry L Orr-Weaver
Journal:  Proc Natl Acad Sci U S A       Date:  2014-10-27       Impact factor: 11.205

Review 3.  Nuclear positioning by actin cables and perinuclear actin: Special and general?

Authors:  Sven Huelsmann; Nicholas H Brown
Journal:  Nucleus       Date:  2014-06-06       Impact factor: 4.197

4.  The temporally controlled expression of Drongo, the fruit fly homolog of AGFG1, is achieved in female germline cells via P-bodies and its localization requires functional Rab11.

Authors:  Irina E Catrina; Livia V Bayer; Giussepe Yanez; John M McLaughlin; Kornelia Malaczek; Ekaterina Bagaeva; Salvatore A E Marras; Diana P Bratu
Journal:  RNA Biol       Date:  2016-08-11       Impact factor: 4.652

5.  Role of the insulin/Tor signaling network in starvation-induced programmed cell death in Drosophila oogenesis.

Authors:  T L Pritchett; K McCall
Journal:  Cell Death Differ       Date:  2012-01-13       Impact factor: 15.828

6.  Hijacking Oogenesis Enables Massive Propagation of LINE and Retroviral Transposons.

Authors:  Lu Wang; Kun Dou; Sungjin Moon; Frederick J Tan; Zz Zhao Zhang
Journal:  Cell       Date:  2018-07-26       Impact factor: 41.582

Review 7.  Cracking the nodule worm code advances knowledge of parasite biology and biotechnology to tackle major diseases of livestock.

Authors:  Rahul Tyagi; Anja Joachim; Bärbel Ruttkowski; Bruce A Rosa; John C Martin; Kymberlie Hallsworth-Pepin; Xu Zhang; Philip Ozersky; Richard K Wilson; Shoba Ranganathan; Paul W Sternberg; Robin B Gasser; Makedonka Mitreva
Journal:  Biotechnol Adv       Date:  2015-05-27       Impact factor: 14.227

8.  Drosophila Inducer of MEiosis 4 (IME4) is required for Notch signaling during oogenesis.

Authors:  Cintia F Hongay; Terry L Orr-Weaver
Journal:  Proc Natl Acad Sci U S A       Date:  2011-08-22       Impact factor: 11.205

9.  Buffy, a Drosophila Bcl-2 protein, has anti-apoptotic and cell cycle inhibitory functions.

Authors:  Leonie Quinn; Michelle Coombe; Kathryn Mills; Tasman Daish; Paul Colussi; Sharad Kumar; Helena Richardson
Journal:  EMBO J       Date:  2003-07-15       Impact factor: 11.598

Review 10.  Diversity of cell death pathways: insight from the fly ovary.

Authors:  Victoria K Jenkins; Allison K Timmons; Kimberly McCall
Journal:  Trends Cell Biol       Date:  2013-08-19       Impact factor: 20.808

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