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+[[!meta title="Evolution of CDK1 Paralog Specializations in a Lineage With Fast Developing Planktonic Embryos."]]
+[[!tag Oikopleura cell_cycle H3S28p]]
+
+Ma X, Øvrebø JI, Thompson EM. 
+
+Front Cell Dev Biol. 2022 Jan 28;9:770939. doi:10.3389/fcell.2021.770939
+
+Evolution of CDK1 Paralog Specializations in a Lineage With Fast Developing Planktonic Embryos.
+
+[[!pmid desc="The last common ancestors of all oiks probably had only one CDK1
+as _Fritillaria borealis_ also has only 1.  Oiks in general have 3 paralogs
+(_a_, _b_, _c_), and _O. dioica_ has 5 (_a_, _b_, _c_, plus _d_ and _e_ which
+appear to originate from _c_).  They are found on chr1 (_c_, _e_), chr2, (_a_,
+_b_) and the XSR of chr3 (_d_).  CycBa is also found on the XSR, and interacts
+with CDK1d for functions essential to meiosis of oocytes.  In contrary to the
+ancestral CDK1 in other animals, the levels of CDK1d oscillate."]]

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@@ -40,6 +40,9 @@ punctate centromere staining at ”late prophase“, a stronger signal (but hard
 to resolve) at metaphase, a weaker signal at anaphase and a weaker or no signal
 at telophase.  Table S1, listing the antibodies used, is missing.
 
+In [[Ma, Øvrebø, and Thompson, 2022|biblio/35155443]] Figure S6, the Abcam
+ab10543 antibody makes broad dots from interphase to meta/anaphase in tadpoles.
+
 The rat monoclonal antibody (Abcam ab10543) stains the centromere-attracting
 body in _O. dioica_, Osaka lab. strain. ([[Nishida and coll.,
 2021|biblio/34755656]]), probably by cross-reactivity.