Cytoskeletal variations in an asymmetric cell division support diversity in nematode sperm size and sex ratios

Development. 2017 Sep 15;144(18):3253-3263. doi: 10.1242/dev.153841. Epub 2017 Aug 21.

Abstract

Asymmetric partitioning is an essential component of many developmental processes. As spermatogenesis concludes, sperm are streamlined by discarding unnecessary cellular components into cellular wastebags called residual bodies (RBs). During nematode spermatogenesis, this asymmetric partitioning event occurs shortly after anaphase II, and both microtubules and actin partition into a central RB. Here, we use fluorescence and transmission electron microscopy to elucidate and compare the intermediate steps of RB formation in Caenorhabditis elegans, Rhabditis sp. SB347 (recently named Auanema rhodensis) and related nematodes. In all cases, intact microtubules reorganize and move from centrosomal to non-centrosomal sites at the RB-sperm boundary whereas actin reorganizes through cortical ring expansion and clearance from the poles. However, in species with tiny spermatocytes, these cytoskeletal changes are restricted to one pole. Consequently, partitioning yields one functional sperm with the X-bearing chromosome complement and an RB with the other chromosome set. Unipolar partitioning may not require an unpaired X, as it also occurs in XX spermatocytes. Instead, constraints related to spermatocyte downsizing may have contributed to the evolution of a sperm cell equivalent to female polar bodies.

Keywords: Asymmetric partitioning; Caenorhabditis elegans; Cytoskeletal reorganization; Non-centrosomal microtubules; Spermatogenesis; Spermiogenesis; X chromosome segregation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Actins / metabolism
  • Animals
  • Asymmetric Cell Division*
  • Caenorhabditis elegans / cytology*
  • Cell Size*
  • Centrosome / metabolism
  • Cytoskeleton / metabolism*
  • Cytoskeleton / ultrastructure
  • Female
  • Hermaphroditic Organisms / cytology
  • Male
  • Meiosis
  • Microtubules / metabolism
  • Models, Biological
  • Sex Ratio*
  • Spermatocytes / cytology
  • Spermatocytes / ultrastructure
  • Spermatogenesis
  • Spermatozoa / cytology*
  • Spermatozoa / ultrastructure

Substances

  • Actins