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An ultrastructural study of germ plasm in spermatogenesis of Xenopus lœvis
J. B. Kerr, K. E. Dixon
Development 1974 32: 573-592;
J. B. Kerr
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K. E. Dixon
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Summary

Spermatogonia and primary diplotene and zygotene spermatocytes contain an electrondense, finely granular substance which is usually closely associated with mitochondria; small patches of this substance also occur close to the nuclear membrane, often in the nuclear pores, and within the nucleus of primary spermatogonia. The fine structure of this substance is very similar to the fine structure of germ plasm in other stages of development, and since an ontogenetic continuity with germ plasm can be demonstrated, it was concluded that this substance is also germ plasm. The substance disappears about pachytene, earlier than in oogenesis where it persists until mid-diplotene, a difference which may be due to the fact that the oocyte stores large quantities of germ plasm in its cortex for the next generation of primordial germ cells. If the presence of the substance in the nuclear pores and within the nucleus is an indicator of synthesis of germ plasm, then synthesis stops in the secondary spermatogonium, which correlates with the subsequent absence of germ plasm from the pachytene spermatocyte stages. It is suggested that the function of the germ plasm in specifying germ line cells is carried out between the gastrula stage and the beginning of meiosis. The three events which take place during this period are (i) the migration of the presumptive primordial germ cells from the endoderm to the genital ridges, (ii) mitosis of the primordial germ cells and subsequently of the oogonia and spermatogonia in the developing gonads and (iii) preparations for meiosis. It is suggested that the mechanism of action of the germ plasm may be in the control of one or more of these processes. Other types of granular cytoplasmic deposits are also described, and their possible relationship to germ plasm discussed.

Footnotes

    • Received December 3, 1973.
    • Revision received February 2, 1974.
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An ultrastructural study of germ plasm in spermatogenesis of Xenopus lœvis
J. B. Kerr, K. E. Dixon
Development 1974 32: 573-592;
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An ultrastructural study of germ plasm in spermatogenesis of Xenopus lœvis
J. B. Kerr, K. E. Dixon
Development 1974 32: 573-592;

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An interview with Swathi Arur

Swathi Arur joined the team at Development as an Academic Editor in 2020. Her lab uses multidisciplinary approaches to understand female germline development and fertility. We met with her over Zoom to hear more about her life, her career and her love for C. elegans.


Jim Wells and Hanna Mikkola join our team of Editors

We are pleased to welcome James (Jim) Wells and Hanna Mikkola to our team of Editors. Jim joins us a new Academic Editor, taking over from Gordan Keller, and Hanna joins our team of Associate Editors. Find out more about their research interests and areas of expertise.


New funding scheme supports sustainable events

As part of our Sustainable Conferencing Initiative, we are pleased to announce funding for organisers that seek to reduce the environmental footprint of their event. The next deadline to apply for a Scientific Meeting grant is 26 March 2021.


Read & Publish participation continues to grow

“I’d heard of Read & Publish deals and knew that many universities, including mine, had signed up to them but I had not previously understood the benefits that these deals bring to authors who work at those universities.”

Professor Sally Lowell (University of Edinburgh) shares her experience of publishing Open Access as part of our growing Read & Publish initiative. We now have over 150 institutions in 15 countries and four library consortia taking part – find out more and view our full list of participating institutions.


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Development presents...

Our successful webinar series continues into 2021, with early-career researchers presenting their papers and a chance to virtually network with the developmental biology community afterwards. Here, Michèle Romanos talks about her new preprint, which mixes experimentation in quail embryos and computational modelling to understand how heterogeneity in a tissue influences cell rate.

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