You are completely correct but some words lean themselves to misunderstandings or preconceptions, which in turn could disolve the purpose of meaningful discussion.
You are right, I agree. The terms were discussed in the OP, thus any misunderstandings can only come from those who did not take the time to read the OP.
Back to business:
Tool kits for multicellularity before the emergence of multicellularity.
It is only until a few years ago that it was thought protein families involved in multicellularity were only present within the multicellular lineages. This old view is consistent with the view that evolution works by the slow accumulation of genes through chance and selection. This view is now a bit outdated.
Take a look at cadherins. Multicellular organisms require protein systems and molecules with adhesive properties in order to build multicellular systems.
Cadherins is one such system. Another system for coordinating the multicellularity signaling system is
protein tyrosine kinases.
In both these cases, the diversity of the these tool kits are greater in unicellular organisms (e.g. Monosiga Brevicollis) that their multicellular counterparts. In the case of tyrosine signaling, tyrosine kinase
signaling machinery in choanoflagellates (e.g. Monosiga Brevicollis) are even more diverse than those in the human counterparts and contain domains in combinations never before observed in the proteins from the multicellular lineage. This means that these shared protein domains that signal and control for multicellularity were present in the last common ancestor between mutlicellilar and unicellular organisms. Divergence from this group resulted in the independent use of the signaling machinery for multicellularity. These tool kits were then used for different purposes. E.g., while the TK signaling machinery is important for multicellularity in multicellular organisms, they appear to be important for bacterial prey capture in unicellular organisms.
Another interesting example is
KNOX and
BELL hox genes families that regulate stem formation in plants. In unicelllar alga, Chlamydomonas, their function is associated with regulation of gamete differentiation.
This data only further demonstrates that the old view of slow accumulation of genetic diversity through chance and selection is outdated, and shows that the genetic material necessary for multicellular transitions were present way before multicellularity emerged.
And increase atmospheric oxygen pressure just unlocked the signaling capabilities of one of these tool kits.