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. 2014 Nov 20;10(11):e1004777. doi: 10.1371/journal.pgen.1004777

Figure 5. SAS-1 is a stable centriolar component recruited very early after fertilization independently of other centriolar proteins.

Figure 5

(A, D, F, I) Schematics of experiments performed in the corresponding figures. (B, G) Embryos stained for GFP to reveal GFP-SAS-1 (yellow) and IFA (magenta). DNA is in cyan. Note that a GFP focus was not detected in some embryos, perhaps due to a very weak signal. However, some embryos exhibit just one very bright signal, supporting a bona fide asymmetry of SAS-1 distribution between the two sperm centrioles. Note that the embryo in B is in telophase of the one-cell stage. (E) Quantification of FRAP experiments performed with sas-1(t1476) GFP-SAS-1 embryos bleached at indicated time points. Centriolar signal intensity was quantified as depicted in (D). A schematic of an experiment performed at pronuclear meeting is shown in (D). (C, H) Quantification of experiments shown in B and G. Note that in C, embryos from the 1- until the 4-cell stage were scored. (J–N) Indicated components were inactivated using RNAi in GFP-SAS-1 hermaphrodites, which were mated with control males that contributed unlabeled paternal centrioles. Embryos were stained for SAS-1 (yellow) and GFP (magenta), except (N), where IFA was used instead of SAS-1 (yellow). DNA is in cyan. N = 10 for each condition.

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