Literature DB >> 6420420

Are annulate lamellae in the Drosophila embryo the result of overproduction of nuclear pore components?

J P Stafstrom, L A Staehelin.   

Abstract

Annulate lamellae are cytoplasmic organelles composed of stacked sheets of membrane containing pores that are structurally indistinguishable from nuclear pores. The functions of annulate lamellae are not well understood. Although they may be found in virtually any eucaryotic cell, they occur most commonly in transformed and embryonic tissues. In Drosophila, annulate lamellae are found in the syncytial blastoderm embryo as it is cleaved to form the cellular blastoderm. The cytological events of the cellularization process are well documented, and may be used as temporal landmarks when studying changes in annulate lamellae. By using morphometric techniques to analyze electron micrographs of embryos, we are able to calculate the number of pores per nucleus in nuclear envelopes and annulate lamellae during progressive stages of cellularization. We find that annulate lamellae pores remain at a low level while nuclear envelopes are expanding and acquiring pores in early interphase. Once nuclear envelopes are saturated with pores, however, the number of annulate lamellae pores increases more than 10-fold in 9 min. Over the next 30 min it gradually declines to the initial low level. On the basis of these results, we propose (a) that pore synthesis and assembly continues after nuclear envelopes have been saturated with pores; (b) that these supernumerary pores accumulate transiently in cytoplasmic annulate lamellae; and (c) that because these pores are not needed by the embryo they are subsequently degraded.

Entities:  

Mesh:

Year:  1984        PMID: 6420420      PMCID: PMC2113103          DOI: 10.1083/jcb.98.2.699

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  30 in total

Review 1.  The nuclear and the cytoplasmic pore complex: structure, dynamics, distribution, and evolution.

Authors:  G G Maul
Journal:  Int Rev Cytol Suppl       Date:  1977

Review 2.  The structure and function of annulate lamellae: porous cytoplasmic and intranuclear membranes.

Authors:  R G Kessel
Journal:  Int Rev Cytol       Date:  1983

3.  Origin, differentiation, distribution and possible functional role of annulate lamellae during spermatogenesis in Drosophila melanogaster.

Authors:  R G Kessel
Journal:  J Ultrastruct Res       Date:  1981-04

4.  Immunological localization of the major architectural protein associated with the nuclear envelope of the Xenopus laevis oocyte.

Authors:  R Stick; G Krohne
Journal:  Exp Cell Res       Date:  1982-04       Impact factor: 3.905

5.  Formation and possible function of annulate lamellae in a planktic foraminifer.

Authors:  M Spindler; C Hemleben
Journal:  J Ultrastruct Res       Date:  1982-12

6.  Studies of nuclear and cytoplasmic behaviour during the five mitotic cycles that precede gastrulation in Drosophila embryogenesis.

Authors:  V E Foe; B M Alberts
Journal:  J Cell Sci       Date:  1983-05       Impact factor: 5.285

7.  A large particle associated with the perimeter of the nuclear pore complex.

Authors:  P N Unwin; R A Milligan
Journal:  J Cell Biol       Date:  1982-04       Impact factor: 10.539

Review 8.  Mechanisms for the incorporation of proteins in membranes and organelles.

Authors:  D D Sabatini; G Kreibich; T Morimoto; M Adesnik
Journal:  J Cell Biol       Date:  1982-01       Impact factor: 10.539

9.  Identification of a major polypeptide of the nuclear pore complex.

Authors:  L Gerace; Y Ottaviano; C Kondor-Koch
Journal:  J Cell Biol       Date:  1982-12       Impact factor: 10.539

10.  Isolation and characterization of a proteinaceous subnuclear fraction composed of nuclear matrix, peripheral lamina, and nuclear pore complexes from embryos of Drosophila melanogaster.

Authors:  P A Fisher; M Berrios; G Blobel
Journal:  J Cell Biol       Date:  1982-03       Impact factor: 10.539

View more
  8 in total

1.  Postmitotic annulate lamellae assembly contributes to nuclear envelope reconstitution in daughter cells.

Authors:  He Ren; Guangwei Xin; Mingkang Jia; Shicong Zhu; Qiaoyu Lin; Xiangyang Wang; Qing Jiang; Chuanmao Zhang
Journal:  J Biol Chem       Date:  2019-05-31       Impact factor: 5.157

2.  Freeze-fracture analysis of structural reorganization during meiotic maturation in oocytes of Xenopus laevis.

Authors:  C A Larabell; D E Chandler
Journal:  Cell Tissue Res       Date:  1988-01       Impact factor: 5.249

3.  Nuclear pore complex assembly studied with a biochemical assay for annulate lamellae formation.

Authors:  E Meier; B R Miller; D J Forbes
Journal:  J Cell Biol       Date:  1995-06       Impact factor: 10.539

4.  Insertional mutation of the Drosophila nuclear lamin Dm0 gene results in defective nuclear envelopes, clustering of nuclear pore complexes, and accumulation of annulate lamellae.

Authors:  B Lenz-Böhme; J Wismar; S Fuchs; R Reifegerste; E Buchner; H Betz; B Schmitt
Journal:  J Cell Biol       Date:  1997-06-02       Impact factor: 10.539

5.  Spontaneous assembly of pore complex-containing membranes ("annulate lamellae") in Xenopus egg extract in the absence of chromatin.

Authors:  M C Dabauvalle; K Loos; H Merkert; U Scheer
Journal:  J Cell Biol       Date:  1991-03       Impact factor: 10.539

6.  Nuclear pore complexes form immobile networks and have a very low turnover in live mammalian cells.

Authors:  N Daigle; J Beaudouin; L Hartnell; G Imreh; E Hallberg; J Lippincott-Schwartz; J Ellenberg
Journal:  J Cell Biol       Date:  2001-07-09       Impact factor: 10.539

7.  A trypsin-sensitive receptor on membrane vesicles is required for nuclear envelope formation in vitro.

Authors:  K L Wilson; J Newport
Journal:  J Cell Biol       Date:  1988-07       Impact factor: 10.539

8.  Pre-assembled Nuclear Pores Insert into the Nuclear Envelope during Early Development.

Authors:  Bernhard Hampoelz; Marie-Therese Mackmull; Pedro Machado; Paolo Ronchi; Khanh Huy Bui; Nicole Schieber; Rachel Santarella-Mellwig; Aleksandar Necakov; Amparo Andrés-Pons; Jean Marc Philippe; Thomas Lecuit; Yannick Schwab; Martin Beck
Journal:  Cell       Date:  2016-07-07       Impact factor: 41.582

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.