Abstract

The katanin microtubule-severing proteins are essential regulators of microtubule dynamics in a diverse range of species. Here we have defined critical roles for the poorly characterised katanin protein KATNAL2 in multiple aspects of spermatogenesis: the initiation of sperm tail growth from the basal body, sperm head shaping via the manchette, acrosome attachment, and ultimately sperm release. We present data suggesting that depending on context, KATNAL2 can partner with the regulatory protein KATNB1 or act autonomously. Moreover, our data indicate KATNAL2 may regulate δ- and ε-tubulin rather than classical α-β-tubulin microtubule polymers, suggesting the katanin family has a greater diversity of function than previously realised. Together with our previous research, showing the essential requirement of katanin proteins KATNAL1 and KATNB1 during spermatogenesis, our data supports the concept that in higher order species the presence of multiple katanins has allowed for subspecialisation of function within complex cellular settings such as the seminiferous epithelium.

Highlights

  • IntroductionThe katanins are members of the ATPases Associated with diverse cellular Activities (AAA) superfamily, and were first identified via the microtubule severing activity of the catalytic KATNA1 (p60) and its regulatory protein, KATNB1 (p80) [1], and their pivotal roles in defining meiotic spindle structure in Caenorhabditis elegans [2,3]

  • We have used spermatogenesis to define the function of the putative microtubule-severing protein kataninlike 2 (KATNAL2)

  • We show that mice with compromised KATNAL2 function are male

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Summary

Introduction

The katanins are members of the ATPases Associated with diverse cellular Activities (AAA) superfamily, and were first identified via the microtubule severing activity of the catalytic KATNA1 (p60) and its regulatory protein, KATNB1 (p80) [1], and their pivotal roles in defining meiotic spindle structure in Caenorhabditis elegans [2,3]. Microtubule severing is used to remodel existing structures, release microtubules from nucleation sites and to generate short stable microtubule fragments that can ‘seed’ new growth and/or be transported around the cell [11,12,13,14]. Reflective of their integral role in microtubule dynamics, Katna and Katnb are highly conserved across the genomes of animals, higher order plants and protozoa.

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