Download - Temperature
TemperatureTemperature
Response to Temperature Stress
Outline
(1) Endothermy in Mammals
(2) Response to Heat Stress
(3) Response to Cold
Geographic Distribution of species is determined, in part, by temperature
How do organisms deal with Temperature Stress?
Temperature
Affects the rates of biochemical reactions, and of physical processes (diffusion, osmosis)
Protein conformation and enzyme function
Affects metabolic rate
Body Temperature
Poikilotherm: body temperature is variable
Homeotherm: body temperature is constant
Ectotherm: regulate body temperature externally (behavior); most are poikilotherms
Endotherm: elevated body temperature using metabolic heat (mammals, birds, tuna, some insects); many are homeotherms
Variation in Body Temperature °C
Ectotherms Endotherms
Marine Deep Sea fish 4-6 Whale 36Frog 22-28 Human 37Housefly 30-33 Rodent 35-37Tropical fish 20-28 Bat 35-39Desert Iguana 36-41 Chicken 40
Dove 39-42
Bee 35-42
Evolution of Body Temperature
Why are endotherms 35-40°C?
Many ectotherms aim for these temperatures as well
Optimal for enzyme activity Faster neuronal, hormonal function Slight elevation: Easier to gain than lose heat Physical properties of water are at an ideal balance of
viscosity, specific heat, and ionization
EndothermyEndothermy
Buffers biochemical reactions against temperature stress
Allows organisms to invade a broader range of habitats
Evolved independently multiple times WHY?
Two Hypotheses:
Thermoregulatory Advantage• Maintain constant body temperature• Easier to maintain a high body T than lower
Aerobic Capacity Advantage• Selection for enhanced physical performance
(endurance, locomotion)• With increased heat production as a secondary effect
Thermoregulation: evolutionary causes?
EndothermyEndothermy
All animals produce heat, but endotherms All animals produce heat, but endotherms produce moreproduce more
(4-8 times)(4-8 times)
Metabolic rate is ~4-10 times higherMetabolic rate is ~4-10 times higherLargest component of energy budgetLargest component of energy budget
Where and How is Body Heat Where and How is Body Heat Produced?Produced?
How is Body Heat Produced?How is Body Heat Produced?
• ATP-producing reactionsATP-producing reactions• ATP-consuming reactionsATP-consuming reactions• Ion pumping (ATP hydrolysis) (~25%)Ion pumping (ATP hydrolysis) (~25%)• Mitochondrial proton leakMitochondrial proton leak• Urea production (~2%)Urea production (~2%)• Glycolysis (~5%)Glycolysis (~5%)• EtcEtc
All Metabolic Activity produces HeatAll Metabolic Activity produces Heat
Mostly in the mitochondria Mostly in the mitochondria 3/4 in abdominal organs (brain, gut, liver, kidney, 3/4 in abdominal organs (brain, gut, liver, kidney, heart, lungs)heart, lungs)some in musclessome in muscles
Cytochrome Cytochrome oxidase activityoxidase activity
50%
100%
Liver
Kidney
Brain
Heart
Mitochondrial Mitochondrial Surface AreaSurface Area
Lizard
Mouse
50%
100%
Liver
Kidney
Brain
Heart
So heat production is directly linked to metabolism…
And also oxygen consumption and food intake
Mechanism of heat production Mechanism of heat production through mitochondrial proton leakthrough mitochondrial proton leak
Typically, the Electron transport chain and oxidative phosphorylation (ATP production) is coupled.
When they are not, the energy released by electron transport is released as heat, rather than used to make ATP
ATP Synthase
In specialized cells of Endotherms, protons leak across the membrane through uncoupling protein 1 (UCP1 = thermogenin)
Such proton diffusion generates heat
This uncoupled reaction occurs to a high degree in brown adipose tissue, which has large numbers of large mitochondria
Cold --> release Norepinephrine
Hydrolyzes triacylglycerols in BAT (Brown Adipose Tissue) cells to release fuels for mitochondrial oxidation
Lipid oxidation proceeds with UCP1 activated
Box 6.1, p. 220
Nonshivering thermogenesis
Increase rate of oxidation of stored lipids
Uncoupling of oxidative phosphorylation from electron transport in the mitochondria
Allows energy to be released as heat rather than stored as ATP
More prominent in cold-adapted mammals, hibernators, newborns
Response to High Response to High Temperature StressTemperature Stress
• Last time we discussed the structure and function of enzymes, which are proteins
• Protein folding depends on thermodynamics, and can be disrupted by high temperatures
• How is protein structure and function maintained under conditions of temperature (or other) stresses?
Ensure correct protein folding
Not only used for temperature stress, but also other stresses (osmotic shock, etc)
Figure: silver staining of Hsps in the cell
Hsp70Hsp70 Heat Shock Proteins
Hsp70
• The fruit fly, Drosophila melanogaster lay their eggs on rotting fruit
• The larvae can experience very high temperatures while growing on the fruit
• They use the enzyme alcohol dehydrogenase (ADH) to break down alcohol that accumulates in the rotting fruit
• They need to protect their proteins and enzymes such as ADH against denaturing under heat stress
Inserting extra copies of Hsp 70 enhanced tolerance of high temperature in Drosophila melanogaster
Extra copy strain: 12 copiesExcision strain: 10 copies
Number of copies affects the degree of hsp expression(the amount of hsp transcribed)
Evolutionary tradeoffs of high Hsp expression?
Cost to growth: Constant (constitutive) expression of hsp inhibits cell proliferation (would inhibit growth)
Cost to Reproduction: decreases rates of age-specific mortality during normal aging, while maternally experienced heat shock depresses the production of mature progeny (Silbermann and Tatar 2000)
Temperatures at which HSPs are induced have evolved to correspond to temperatures that are stressful for a given species or cell type.
Antarctic organisms begin to express HSPs at relatively low temperatures (< 10°C) (Vayda and Yuan 1994)
Some hyperthermophiles do not express HSPs until temperatures exceed 60°C (Trent, Osipiuk et al. 1990; Ohta, Honda et al. 1993; Polla, Kantengwa et al. 1993; Trent, Gabrielsen et al. 1994)
Hypothermic regions of mammals (e.g., testis) express HSPs at lower temperatures than normothermic organs (Sarge 1995; Sarge, Bray et al. 1995)
Canalization (flip side of plasticity)
Influenced by developmental stability
Stress could disrupt canalization and lead to new phenotypes
Particular genes might be important for maintaining developmental stability and buffer against perturbations
Queitsch et al. 2002. Nature. 417:618-624
A potential “plasticity gene”in response to environmental stress
Heat-shock protein 90 (Hsp 90) chaperones the maturation of many regulatory proteins
In Drosophila melanogaster, buffers genetic variation in morphogenetic pathways
Reducing Hsp90 function in Drosophila or Arabidopsis produces an array of morphological phenotypes, revealing hidden genetic variation
Development abnormalities in HSP90 deficient
Drosophila
(Rutherford and Lindquist. 1998.
Nature)
Study criticized because fitness
consequences were not examined
Normal
Hsp90 inhibited
Normal
Hsp90 inhibited
Unlike case of Drosophila, diverse phenotypes here were not “monstrous” but potentially adaptive
Dependence on Hsp90 for developmental stability varied
Potential Mechanism:
Under stress, Hsp90 is recruited to maintain protein folding and the function of proteins
Ability to maintain developmental pathway is exceeded
Adaptation to Cold
Differences between Aquatic Differences between Aquatic Vertebrates vs Invertebrates???Vertebrates vs Invertebrates???
Because of their Freshwater originBecause of their Freshwater originand osmotic properties, cold and osmotic properties, cold temperatures pose problems for fishestemperatures pose problems for fishes
Cold temperatures pose problems for Cold temperatures pose problems for fish in water because they are fish in water because they are hyposmotichyposmotic
Freezing point is higher in their Freezing point is higher in their extracellular fluids relative to ambient extracellular fluids relative to ambient seawaterseawater
Osmotic/Temperature InteractionsOsmotic/Temperature Interactions
Freshwater Freezes at 0°C
Seawater Freezes at -1.89°C
But hyposmotic fish might freeze at -0.7°C
Solutions
Cold water fish have more NaCl in extracellular fluids
Uses osmolytes such as glycerol (works better than NaCl)
Antifreeze proteins
Antifreeze proteins
200x more effective than NaCl
Not freeze until -6°C
Hot commodity these days
(cryopreservation, food preservation, health)
Antarctic Fish Pagothenia borchgrevinki
Molecular structure of an antifreeze glycoproteinSome are multigene families that have experienced
multiple gene duplications
Diagram of the adsorption-inhibition mechanism of AFGPs (modified from Eastman, 1993)
J Mol Evol (2002) 54:403–410
When mapped onto the three-dimensional structure of the fish antifreeze type III antifreeze structure, these codons correspond to amino acid positions that surround but do not interrupt the putative ice-binding surface.
The selective agent may be related to efficient binding to diverse ice surfaces or some other aspect of AFP function.
Most of the Amino Acid Substitutions are at the Ice binding Surfaces of the AntiFreeze Proteins