Sex chromosomes in plants Flashcards
(9 cards)
What are the main types of plant sexual systems?
Monomorphic Systems (one flower type per population):
- Monocliny (~85%): Hermaphroditic flowers (both male & female organs).
- Gynomonoecy: Female and bisexual flowers on the same plant.
- Andromonoecy: Male and bisexual flowers on the same plant.
- Monoecy (6–7%): Separate male and female flowers on the same plant.
Dimorphic Systems (two flower types per population):
- Distyly (<1%): Two morphs differing in stamen/style lengths.
- Gynodioecy (<1%): Coexistence of female plants & hermaphrodites.
- Dioecy (5–6%): Separate male & female plants.
- Androdioecy (<1%): Coexistence of male plants & hermaphrodites.
Evolution of dioecyfrom hermaphroditism?
Evolution often occurs through intermediate steps like gynodioecy or monoecy.
Step 1: A male-sterile mutation spreads if selfing causes inbreeding depression, making outcrossing more beneficial.
Step 2: A female-suppressing mutation spreads if it allows better resource allocation to pollen production, when tehre is enough female individuals.
Step 3: Recombination suppression ensures sex-determining genes remain linked on the Y/W chromosome. (Two-locus model)
What are the key genes involved in plant sex determination?
SOFF (Suppressor of Female Function): Found in Asparagus officinalis, essential for male development.
aspTDF1: A tapetum-specific gene required for male fertility in Asparagus. Taptum needed in Pollen development
In Asparagus two-locus model. SOFF and TDF1 are Y-linked Sex DetermInation Region (Y- SDR)
Shy Girl (SyGl): A female-suppressing factor on the Y chromosome in Kiwi, expressed in carpel primordia. Mutant makes nornal pollen but is female sterile. (repressor of cytokinin signaling)
Friendly Boy (FrBy): A male-fertility factor on the Y chromosome in Kiwi. In mutant the tapetum does not develop like in the control plants.
ARR17: A single-gene sex switch in Poplar (Populus)—its suppression leads to male development.
GPAT3, CYP703, LOG: Sex-determining genes in date palm, affecting male fertility and female organ development.
What processes contribute to the degeneration of a non-recombining, permanently heterozygous region.
1) The effective population size (Ne) of a Y-chromosome is only ¼ of that of a diploid autosomal region/chromosome. Therefore, the effect of drift relative to that of selection is increased.
2) Suppressed recombination leads to Hill-Robertson interference.
Why is dioecy relatively rare in plants?
Only 5–6% of angiosperms are dioecious.
- Trade-offs: Male-only plants do not produce seeds, reducing their reproductive success.
- Outcrossing vs. Reproductive Assurance:Hermaphrodites can self-fertilize if needed, whereas dioecious plants require a pollinator.
Resource allocation: Male and female plants might evolve different growth patterns due to differences in reproductive investment.
What are plant sex chromosomes?
- Chromosomes that determine male or female development.
- They evolve from autosomes and may have suppressed recombination.
- Found in dioecious species (e.g., asparagus, kiwi, poplar, persimmon)
What are the two main models of sex determination in plants?
Single-locus model: One dominant gene determines sex (e.g., poplar, persimmon).
Two-locus model: Two linked genes control male vs. female traits (e.g., kiwi, asparagus, date palm).
How does recombination suppression evolve on sex chromosomes?.
Ensures that sex-determining genes stay linked.
Possible mechanisms:
* Chromosomal inversions block recombination.
* Hemizygous regions (genes only on Y/W, missing on X/Z).
* Recombination cold spots or heterochiasmy (lower recombination rates in males).
* Over time, this creates evolutionary strata, expanding non-recombining regions
Why does the Y/W chromosome degenerate over time?
Lack of recombination prevents efficient selection.
Key processes:
* Muller’s Ratchet: Accumulation of slightly harmful mutations.
* Hill-Robertson interference: Reduced selection efficiency.
* Insertion of repetitive elements & transposable elements.
In some cases, dosage compensation evolves to counteract gene loss.