Chapter 40 Flashcards
Reproductive Development
Angiosperms represent an evolutionary innovation with their production of flowers and fruits
Plants go through developmental changes leading to reproductive maturity by adding structures to existing ones with meristems
Initiation of Flowering
Once plants are competent to reproduce, a combination of factors – including light, temperature, and both promotive and inhibitory internal signals – determines when a flower is produced
Undergo phase change – subtle or obvious
Phase Change
Internal developmental changes allow plants to obtain competence to respond to external or internal signals that trigger flower formation
May be morphologically obvious or very subtle
Examples of Phase Changes
The lower branches in the oak tree retain their leaves in the winter, because these lower branches were initiated by juvenile meristems and have not made a phase change. Juvenile ivy makes adventitious roots that can cling to walls, but after a phase change mature ivy lacks the ability to produce adventitious roots.
Delay of Flowering
In Arabidopsis, the gene embryonic flower (emf) prevents early flowering
emf mutants flower immediately.
Flowering is the default state
Many mechanisms have evolved to delay flowering
Inducing Flowering
The juvenile-to-adult transition can be induced by overexpressing a flowering gene called LEAFY
LEAFY (L F Y) was cloned in Arabidopsis and replaced with a viral promoter that results in constant, high levels of L F Y transcription
Overexpression of L F Y in aspen causes flowering to occur in weeks instead of years
Accelerated Phase Change
Normally aspen trees grow for several years before producing flowers. Overexpression of the Arabidopsis flowering gene LFY causes rapid flowering in transgeneic aspen.
Four genetically regulated pathways to flowering have been identified
-The light-dependent pathway
-The temperature-dependent pathway
-The gibberellin-dependent pathway
-The autonomous pathway
Plants can rely primarily on one pathway, but all four pathways can be present
Light-Dependent Pathway
Also termed the photoperiodic pathway
Keyed to changes in the proportion of light to dark in the daily 24-hr cycle (day length)
Short-day plants flower when daylight becomes shorter than a critical length
Long-day plants flower when daylight becomes longer than a critical length
Day-neutral plants flower when mature regardless of day length
Obligate and Facultative Plants
In obligate long- or short-day plants there is a sharp distinction between short and long nights, respectively
In facultative long- or short-day plants, the photoperiodic requirement is not absolute
Flowering occurs more rapidly or slowly depending on the length of day.
Manipulation of Photoperiod
Using light as a cue allows plants to flower when abiotic conditions are optimal
Manipulation of photoperiod in greenhouses ensures that short-day poinsettias flower in time for the winter holidays
Phytochrome and Cryptochrome
Conformational change in a phytochrome (red-light sensitive) or cryptochrome (blue-light sensitive) light-receptor molecule triggers a cascade of events that leads to the production of a flower
In Arabidopsis, regulate via the gene CONSTANS (C O) which encodes a transcription factor that turns on genes that are needed for flowering
This signaling cascade leads to expression of L F Y
Phytochrome regulates the transcription of C O
CONSTANS
C O protein is produced day and night
The levels of C O are maintained in accordance with the circadian clock
Levels of C O mR N A are lower at night because of targeted protein degradation by ubiquitin
Phytochrome causes an increase in transcription at daybreak
Cryptochrome prevents degradation by the ubiquitin-dependent pathway during the day
Temperature-Dependent Pathway
Some plants require a period of chilling before flowering – vernalization
Described in the 1930s by Ukrainian scientist T.D. Lysenko.
Winter wheat would not flower without a period of chilling.
Seeds could be chilled and planted in the spring.
Gibberellin-Dependent Pathway
Decreased levels of gibberellins have been shown to delay flowering in some species.
Gibberellin has been shown to bind to the promoter of the L F Y gene, which supports a model where gibberellin induces an increase in L F Y gene expression.
This would directly affect flowering.
Autonomous Pathway
Does not depend on external cues except for basic nutrition
Presumably delays flowering
A balance between floral promoting and inhibiting signals may regulate when flowering occurs
Can test determination for flowering by changing the environment and ascertaining whether developmental fate has changed
Flowering Pathways
The four flowering pathways lead to an adult meristem becoming a floral meristem
Activate or repress the inhibition of floral meristem identity genes.
The floral meristem identity genes: L F Y and AP1
Turn on floral organ identity genes.
Define the four concentric whorls.
Sepal, petal, stamen, and carpel.
Explains how 3 classes of floral organ identity genes can specify 4 distinct organ types
-Class A genes alone – Sepals
-Class A and B genes together – Petals
-Class B and C genes together – Stamens
-Class C genes alone – Carpels
When any one class is missing, aberrant floral organs occur in predictable positions
A B C model cannot fully explain specification of floral meristem identity
Class D genes are essential for carpel formation
But does not explain why plants lacking A, B, and C gene function produce four whorls of sepals rather than leaves
Class E genes SEPALATA (S E P)
S E P proteins interact with class A, B, and C proteins that are needed for the development of floral organs.
Modified A B C D E model was proposed
Flower Structure
Floral organs are thought to have evolved from leaves
A complete flower has four whorls
Calyx, corolla, androecium, and gynoecium.
An incomplete flower lacks one or more of the whorls
Calyx
Consists of flattened sepals
Corolla
Consists of petals
Androecium
Collective term for all the stamens (male structures) of a flower
Stamen consists of a filament and an anther.
Gynoecium
Collective term for all carpels (female structures) of a flower
Carpel consists of ovary, style, and stigma.
Ovules produced in ovary.
Trends in Floral Specialization
2 major trends
Floral parts have grouped together
Floral parts lost or reduced
Modifications often relate to pollination mechanisms
Trends in Floral Symmetry
Primitive flowers are radially symmetrical
Advanced flowers are bilaterally symmetrical
Genetic Regulation of Asymmetry
Snapdragon flowers normally have bilateral symmetry, like the one shown here on the left. The CYCLOIDEA gene regulates floral symmetry, and cycloidea mutant snapdragons, like the one on the right, have radially symmetrical flowers.
Gamete Production
Alternation of generations
Diploid sporophyte → haploid gametophyte
In angiosperms, the gametophyte generation is very small and is completely enclosed within the tissues of the parent sporophyte
Male gametophyte – pollen grains.
Female gametophyte – embryo sac.
Reproductive Organs of Angiosperms
Gametes are produced in separate, specialized structures of the flower
Reproductive organs of angiosperms differ from those of animals in two ways
Both male and female structures usually occur together in the same individual
Reproductive structures are not permanent parts of the adult individual