Literature DB >> 7961137

Centriole development and formation of the flagellum during spermiogenesis in the ostrich (Struthio camelus).

J T Soley1.   

Abstract

The formation and development of the ostrich sperm tail follows the general pattern described for vertebrate sperm but differs in a number of important aspects when compared with other nonpasserine birds. Midpiece formation is characterised by the development of a long (3 microns) distal centriole which determines the length of the midpiece. The distal centriole surrounds a pair of microtubules embedded in a core of dense material. A prominent annulus, which remains stationary during spermiogenesis, demarcates the midpiece/principal piece junction. Ostrich spermatids display similar cytoplasmic densities (chromatoid body, annulus, granulated bodies, reticulated bodies and mitochondria-associated material) to those observed in mammalian spermatids. In the ostrich, however, the chromatoid body is not observed to contribute towards the formation of the annulus while the granulated bodies develop within radial bodies and not in their vicinity as in mammals. Whereas in mammals granulated bodies have been linked to coarse fibre formation they appear to perform a limited function in ostrich spermatids as only rudimentary outer dense fibres are formed. No specific role is attributed to the reticulated bodies but the mitochondria associated material is implicated in the formation of intermitochondrial cement. The formation of the principal piece and end piece of the flagellum is modelled on that of the mammalian spermatid. The axoneme emerges from the free end of the distal centriole and the ribs and longitudinal columns are progressively formed from a layer of amorphous material situated between the axoneme and the plasmalemma. The end piece is formed by an extension of the principal piece consisting of axonemal microtubules closely surrounded by the plasmalemma. The formation of a long distal centriole containing a central pair of microtubules, the stationary nature of the annulus and the presence of a ribbed fibrous sheath around the principal piece distinguishes spermiogenesis in the ostrich and rhea from that of other nonpasserine birds. These features appear to be characteristic of more primitive avian families.

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Year:  1994        PMID: 7961137      PMCID: PMC1166760     

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  31 in total

1.  The head, neck and midpiece of cock spermatozoa examined with the transmission electron microscope.

Authors:  M R Bakst; B Howarth
Journal:  Biol Reprod       Date:  1975-06       Impact factor: 4.285

2.  The early development of the tail and the transformation of the shape of the nucleus of the spermatid of the domestic fowl, Gallus gallus.

Authors:  F Okamura; H Nishiyama
Journal:  Cell Tissue Res       Date:  1976-06-28       Impact factor: 5.249

3.  The distal centriole in guinea pig spermiogenesis.

Authors:  M Gordon
Journal:  J Ultrastruct Res       Date:  1972-05

4.  The chromatoid body in mouse spermatogenesis: evidence that it may be formed by the extrusion of nucleolar components.

Authors:  D E Comings; T A Okada
Journal:  J Ultrastruct Res       Date:  1972-04

5.  Observations on the fine structure and relationships of the chromatoid body in mammalian spermatogenesis.

Authors:  D W Fawcett; E M Eddy; D M Phillips
Journal:  Biol Reprod       Date:  1970-02       Impact factor: 4.285

6.  Observations on the fine structure of spermatozoa in the testis and excurrent ducts of the male fowl, Gallus domesticus.

Authors:  M D Tingari
Journal:  J Reprod Fertil       Date:  1973-08

7.  The behaviour of centrioles and the formation of the flagellum in rooster and drake spermatids.

Authors:  M Maretta
Journal:  Cell Tissue Res       Date:  1977-01-12       Impact factor: 5.249

8.  The mammalian spermatozoon.

Authors:  D W Fawcett
Journal:  Dev Biol       Date:  1975-06       Impact factor: 3.582

9.  Fine structural modifications of the rat chromatoid body during spermiogenesis.

Authors:  F R Susi; Y Clermont
Journal:  Am J Anat       Date:  1970-10

10.  Ultrastructural studies on the differentiation of spermatids in the domestic fowl.

Authors:  V K Gunawardana; M G Scott
Journal:  J Anat       Date:  1977-12       Impact factor: 2.610

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  6 in total

1.  Nuclear morphogenesis and the role of the manchette during spermiogenesis in the ostrich (Struthio camelus).

Authors:  J T Soley
Journal:  J Anat       Date:  1997-05       Impact factor: 2.610

Review 2.  Transition Zone Migration: A Mechanism for Cytoplasmic Ciliogenesis and Postaxonemal Centriole Elongation.

Authors:  Tomer Avidor-Reiss; Andrew Ha; Marcus L Basiri
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-08-01       Impact factor: 10.005

Review 3.  Spermiogenesis in birds.

Authors:  Tom A Aire
Journal:  Spermatogenesis       Date:  2014-10-30

Review 4.  Rapid Evolution of Sperm Produces Diverse Centriole Structures that Reveal the Most Rudimentary Structure Needed for Function.

Authors:  Tomer Avidor-Reiss
Journal:  Cells       Date:  2018-06-26       Impact factor: 6.600

5.  A novel transient structure with phylogenetic implications found in ratite spermatids.

Authors:  Lizette du Plessis; John T Soley
Journal:  BMC Evol Biol       Date:  2013-05-26       Impact factor: 3.260

6.  Ultrastructural differentiation of spermiogenesis in Scincus scincus (Scincidae, Reptilia).

Authors:  Mukhtar Ahmed; O A Aldokhi; E S Alenezy
Journal:  Saudi J Biol Sci       Date:  2016-11-02       Impact factor: 4.219

  6 in total

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