Presently-Department of Biological Sciences, University of Delaware, Newark, Delaware 19701
SPE-11 is a sperm protein required to initiate embryonic development. Mutations of the spe-11 gene result in a strict paternal-effect lethal phenotype. Wild-type oocytes fertilized by sperm from homozygous spe-11 males leads to abnormal development, but the reciprocal interaction, spe-11 mutant oocytes fertilized by wild-type male sperm, results in normal development (Hill et al. 1989). Sperm from homozygous spe-11 males are morphologically normal and do not display motility defects (L’Hernault et al. 1988). However, the absence of functional SPE-11 results in embryonic failure at early stages. Embryonic defects include failure to complete oocyte meiosis (an event that takes place upon fertilization), formation of a weak eggshell, and improper orientation of the first mitotic spindle (Hill et al. 1989). In addition, Spe-11 embryos fail to complete cytokinesis during the first division resulting in multinucleated one-cell embryos that eventually die (Hill et al. 1989). The embryonic lethality phenotype conferred by spe-11 mutant sperm is rescued when SPE-11 is ectopically expressed in oocytes demonstrating that SPE-11 functions during early embryogenesis and is not required during sperm development (Browning and Strome 1996). Furthermore, SPE-11 expression in oocytes did not disrupt oocyte activation because these oocytes were still capable of fertilization and did not precociously form an eggshell (i.e. prior to fertilization, Browning and Strome 1996).
SPE-11 is a 299 amino acid protein with no significant similarity to other proteins. SPE-11 is first detected in spermatocytes in the gonad of males as foci that eventually unite to form a ring around the condensed DNA of mature sperm (Browning and Strome 1996). It is predicted to be a very highly hydrophilic protein with five potential nuclear localization sequences (NLS) (Browning and Strome 1996). SPE-11 has no obvious protein domains (Browning and Strome 1996). To define functional units of the SPE-11 protein, we generated a series of GFP::SPE-11 mutant constructs along with a GFP::SPE-11 rescuing construct (Figure 1A) and created transgenic worm lines in the null spe-11(ok2143) background (deletion of exons two through six out of seven total exons) through microparticle bombardment. To determine functionality of each SPE-11 mutant construct we assayed the transgenic lines for SPE-11 localization in late meiotic prophase and in post-meiotic sperm and for rescue of the embryonic lethality phenotype. Similar to previous reports of SPE-11 localization, the wild-type GFP-SPE-11 construct forms foci around diplotene nuclei that eventually coalesce into a perinuclear ring in spermatids (Browning and Strome 1996) and rescues embryonic lethality (Avg. number of viable progeny=175.3, Figure 1B and 1C).
We started our mutant analysis by creating a single integrated, transgenic line carrying a mutant version of the first putative NLS (GFP::SPE-11NLS1). GFP::SPE-11NLS1 both rescues the embryonic lethality of the spe-11(ok2143) mutant and localizes correctly in the male germ line (Figure 1B and 1C). We have also generated a single integrated line with the fifth putative NLS mutated (GFP::SPE-11NLS5). This line localizes correctly during the diplotene substage of meiotic prophase, however it fails to encircle the nuclei of post-meiotic sperm and fails to rescue the embryonic lethality of the spe-11(ok2143) mutant (Figure 1B and 1C). This failed rescue along with the localization defect suggests that the amino acids mutated in GFP::SPE-11NLS5 are important for SPE-11 function and localization. We also generated a SPE-11 construct in which three basic amino acids in the last ten amino acids of the C-terminus are changed to Ala (GFP::SPE-11AAAmut). Note that the GFP::SPE-11NLS5 mutant has two additional basic residues changed to Ala (see Reagents section). Interestingly, the GFP::SPE-11AAAmut mutant had a wild-type localization pattern, yet it completely fails to rescue the embryonic lethality of the spe-11(ok2143) mutant (Avg. number of viable progeny=4.6, Figure 1B and 1C).
The majority of existing spe-11 mutant alleles truncate the SPE-11 protein suggesting that the C-terminus is very important for function. To test the importance of the C-terminus on SPE-11 function we generated an additional transgenic line, one in which only the last five amino acids are removed (GFP::SPE-11∆295-299). This line has a significantly lower number of viable progeny than the GFP::SPE-11 rescuing construct (p<0.05, Figure 1B). GFP::SPE-11∆295-299 localization was similar to GFP::SPE-11 in diplotene stage nuclei, however, it fails to localize correctly in post-meiotic sperm (Figure 1C) suggesting that even the most C-terminal end of the protein (i.e. the last five amino acids) is essential for localization. Interestingly, while embryonic viability was severely reduced in the GFP::SPE-11∆295-299 line (Avg. number of viable progeny=31.9, Figure 1B and 1C), several progeny survived to adulthood.
In summary, we have identified several critical amino acids required for proper SPE-11 localization and function. The putative NLS5 and the extreme C-terminus are required for both localization and function. While not required for localization, analysis of the GFP::SPE-11AAA mutant has identified three critical amino acids in the C-terminus that are required for SPE-11 function. Recreation of these alleles in the endogenous spe-11gene, using CRISPR/Cas9 genome editing, would be interesting to pursue.
MethodsRequest a detailed protocol
All strains were cultured using standard conditions (Brenner 1973). For the creation of transgenic spe-11 animals, the promoter region, open reading frame, and 3’UTR of spe-11 were cloned into separate entry vectors using Gateway technology (Invitrogen). These three entry clones plus an entry clone carrying GFP were recombined into a destination vector with a wild-type unc-119 gene. Mutant unc-119(ed3) animals were transformed by biolistic transformation (or bombardment) with the destination clone (Wilm et al. 1999). Postbombardment, non-Unc animals were picked to determine which lines were integrated and which were extrachromosomal lines. At least two lines were generated for each spe-11 construct and only integrated lines were used for analysis in this study. Lines carrying the spe-11 transgenes were crossed into the spe-11(ok2143) background balanced over hT2. To visualize chromosomes, itIs37 [mCherry::H2B] was crossed into each spe-11(ok2143)/hT2 transgenic line. All analysis was performed on animals homozygous for spe-11(ok2143), itIs37 [mCherry::H2B], and the spe-11 transgene. The average number of live progeny for each strain was determined by picking single L4 hermaphrodites and transferring the animal to fresh plates every 24 h until no additional embryos were produced. The number of hatched larvae were counted after each 24-hour period. SPE-11 localization was determined through live image analysis of adult males. Adult males 24 h post L4 were anesthetized with 2 mM levamisole (Sigma), mounted on an agarose pad, and covered with a coverslip. Image collection was performed using a Nikon Eclipse E800 spinning disk confocal microscope and MetaMorph imaging software. Images were processed and analyzed using Fiji (Schindelin et al. 2012).
AG583: spe-11(ok2143)/hT2 I; itIs37 [pie-1p::mCherry::his-58 + unc-119(+)]
AG584: spe-11(ok2143)/hT2 I; avIs146 [pUNC-119(+) + spe-11p::GFP::spe-11::spe-11 3’UTR]; itIs37
AG585: spe-11(ok2143)/hT2 I; avIs149 [SPE-11NLS1 mutant: PKKKS (amino acids 18-22) to PAAAS]; itIs37
AG586: spe-11(ok2143)/hT2 I; avIs152 [SPE-11∆295-299]; itIs37
AG587: spe-11(ok2143)/hT2 I; avIs159 [SPE-11AAA mutant: Sequence change: KFYRK (amino acids 289-293) to AFYAA]; itIs37
AG588: spe-11(ok2143)/hT2 I; avIs161 [SPE-11NLS5 mutant: Sequence change: KKSLKSVVRNVQKFYRK(amino acids 277-293) to KKSLASVVANVQAFYAA]; itIs37
We would like to thank the members of the Golden, O’Connell, and Cohen-Fix Labs for their helpful discussions.
This work was supported by the Intramural Research Program of the National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases
Reviewed BySusan Strome
HistoryReceived: May 12, 2020
Revision received: May 19, 2020
Accepted: May 19, 2020
Published: May 21, 2020