Genome complexity: how plants avoid inbreeding II (Introduction)

by David Turell , Thursday, July 26, 2018, 04:57 (2312 days ago) @ David Turell

Another view of the poor Darwin approach:

https://evolutionnews.org/2018/07/three-ways-that-plants-defy-darwins-mechanism/

"People know better than to marry their relatives, but how can a blind flower, with no brain or eyes, recognize “self” so as to prevent fertilizing itself? It’s a trick that both gametes have to cooperate on. A mutation in the pollen that enables it to recognize self won’t help if the ovum doesn’t get a corresponding mutation. The Austrian IST researchers were curious about this and decided to take a look.

"In plants such as snapdragons and Petunia, when the pollen lands on the stigma, it germinates and starts growing. The stigma, however, contains a toxin (an SRNase) that stops pollen growth. Pollen in turn has a team of genes (F-box genes) that produce antidotes to all toxins except for the toxin produced by the “self” stigma. Therefore, pollen can fertlize [sic] when it lands on stigma that does not belong to the same plant, but not when it lands on the plant’s own stigma. It may seem like a harsh system, but plants can use this toxin-antidote system to ensure that they only mate with a genetically different plant. This is important as self-fertilization leads to inbreeding, which is detrimental for the offspring.

"Do you see a problem for neo-Darwinism? The stigma basically has a lock that the “self” pollen cannot unlock. The pollen, though, has a key that only works on other flowers’ locks. How could such lock-and-key systems arise in a single plant that will work on unrelated plants? They not only have to evolve the toxin and the antidote, but ensure that the key doesn’t work locally — only with unrelated plants. And that’s not the only conundrum. NSR systems use a different trick. The authors puzzle over how this one evolved:

"In non-self recognition systems, the male (pollen) and female (stigma) genes work together as a team to determine recognition, so that a particular variation of the male- and female-genes forms a mating type. Non-self recognition systems are found all around us in nature and have an astonishing diversity of mating types, so the big question in their evolution is: how do you evolve a new mating type when doing so requires a mutation in both sides? For example, when there is a change in the female side (stigma), it produces a new toxin for which no other pollen has an antidote – so mating can’t occur. Does this means [sic] that there needs to be a change in the male side (pollen) first, so that the antidote appears and then waits for a corresponding change in the stigma (female side)? But how does this co-evolution work when evolution is a random process? Is there a particular order of mutations that is more likely to create a new mating type?

***

"Through theoretical analysis and simulation, the researchers investigated how new mating types can evolve in a non-self recognition system. They found that there are different pathways by which new types can evolve. In some cases this happens through an intermediate stage of being able to self-fertilize; but in other cases it happens by staying self-incompatible. They also found that new mating types only evolved when the cost of self-fertilization (through inbreeding) was high. Being incomplete – i.e., having missing F-box genes that produce antidotes to female toxins — was found to be important for the evolution of new mating types: complete mating types (with a full set of F-Box genes) stayed around for the longest time, as they have the highest number of mating partners. New mating types evolved more readily when there was [sic] less mating types in the population. Also, the demographics in a population affect the evolution of non-self recognition systems: population size and mutation rates all influence how this system evolves.

"The analytical model worked in the committee, but does it work in the real world? In a model, you can assume that beneficial mutations will arise on cue. Nature, however, doesn’t work that way. Their model didn’t compare very well with real flowers:

"So although it seems like having a full team of F-box pollen genes (and therefore antidotes) is the best way for new mating types to evolve, this system is complex and can change via a number of different pathways. Interestingly, while the researchers found that new mating types could evolve, the diversity of genes in their theoretical simulations were fewer compared to what is seen in nature. For Melinda Pickup, this observation is intriguing: “We have provided some understanding of the system, but there are still many more questions and the mystery of the high diversity in nature still exists.'”

Comment: Obviously Darwinists have no idea how the diversity mechanism happened.