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Description : Check out this medical presentation on Beckwith-Wiedemann Syndrome, which is titled "Genomic Conflicts, Health and Disease", to know about the genomic conflicts and how are they involved in health and disease.

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Published on : May 10, 2021 | Views : 1220 | Downloads : 1

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Slide 1-

Genomic Conflicts, Health and Disease What are genomic conflicts and how are they involved in health and disease? (2) Main forms of genomic conflict Parent-offspring conflict (b) Genomic-imprinting conflict (c) Sexual conflict
Slide 2-

The logic & dynamics of genomic evolutionary conflict, in relation to health and disease Frank & Crespi 2011, PNAS
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r = 1/2 r = 1/4 (a) Parent-offspring conflict is due to higher relatedness to self/own offspring than to sib/nieces, nephews
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Parent-offspring conflict Parents value offspring equally. Each offspring values itself 2 times more than it values its sibling. Parents will prefer an equitable distribution of parental investment. Offspring will prefer an inequitable distribution of parental investment, with more to self Conflict begins in the womb. Autosomes: X chromosome alleles? Y chromosome alleles?
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Mom Mom maximizes her inclusive fitness at a lower level of maternal investment than the level that maximizes inclusive fitness for any one offspring Selection for alleles in mom ‘for’ adaptations that constrain investment Selection of alleles in offspring ‘for’ adaptations to take more from mom, to the point that negative effects on other sibs are not too great Kid MAIN STAGES OF CONFLICT: (1) Survival of conceptus (2) Growth in the womb (3) Survival at birth (4) Investment in childhood (5) Inheritance as adult Strategies (variation) available?
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Mother-offspring conflict example Mother has 100 units to invest in kids Three kids to invest in: Options A 33 33 33 B 50 50 0 C 100 0 0 KIDS 1 2 3 Mothers fitness Offspring 1’ s fitness A 3(.5) = 1.5* 0.5 + 2(.5)(.5)=1.0 B 2(.7) = 1.4 0.7 + 1(.5)(.7)=1.05* C 1(.9) = 0.9 0.9 + 0(.5)(0.9)=0.9 Units->Survival 33->.5 50->.7 100->.9
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Conflict can exist over (1) whether or not to ‘miscarry’ (2) invasiveness of the placenta (3) the nutrient quality of maternal blood -> blood glucose (4) the volume of blood reaching the placenta -> blood pressure
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Maternal provisioning of a fetus is associated with an ‘opportunity cost’ The opportunity cost translates into lower expected fitness through other offspring If extra resources are transferred to a given embryo (you) -> the embryo’s (your ) expected fitness increases -> the mother’s expected fitness via other offspring decreases TRADEOFF between current & future reproduction
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Conceptus @ 9 days old
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Manifestations of maternal-fetal conflict Spontaneous abortion - Should mom maintain the pregnancy? Depends on the quality of the fetus and state of the mother. These hinge on cost/benefit issues in relation to possible future pregnancies. AND WHO is in CONTROL of what? POSSIBILITIES Mother and baby Both ‘want’ pregnancy maintained Baby ‘wants’ pregnancy maintained, mother does not CONFLICT Neither ‘wants’ pregnancy maintained - WHY? WHEN? What is a conceptus to do? Shout that they are here and ‘take over’ the system that maintains pregnancy as rapidly as possible
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anterior pituitary corpus luteum uterus Pregnancy is maintained via the production of LH and LH’s stimulation of progesterone (P) production. Temporary endocrine structure, from ovarian follicle
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anterior pituitary corpus luteum uterus placenta luteinizing hormone human chorionic gonadotropin hCG bypasses this pathway and stimulates the corpus luteum to produce progesterone and by the 8th week of pregnancy, produces enough P to sustain pregnancy on its own.
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anterior pituitary corpus luteum uterus placenta luteinizing hormone progesterone chorionic gonadotropin progesterone hCG bypasses this pathway and stimulates the corpus luteum to produce progesterone and by the 8th week of pregnancy, produces enough progesterone to sustain pregnancy on its own.
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Conflicts over food for the growing fetus: Invasion of the placenta into the uterine wall. Allows fetus to prevent cut-off of blood flow (modify spiral arteries), access matermal blood efficiently. Disruption of the conflict system: pre-eclampsia (2) Fast food for baby - amount of food depends on glucose levels in maternal blood - you want more than mom wants to give you. Insulin keeps blood sugar from getting dangerously high. hPL (placental lactogen) blocks (bonds) maternal insulin. Disruption of the conflict system: gestational diabetes (3) More blood please! Amount of food also depends on maternal blood pressure - you want mom’s blood pressure to be higher Disruption of the conflict system: pre-eclampsia
Slide 15-

“The border zone … is not a sharp line, for it is in truth the fighting line where the conflict between the maternal cells and the invading trophoderm takes place, and it is strewn with such of the dead on both sides as have not already been carried off the field or otherwise disposed of.” Johnstone (May 1914) Journal of Obstetrics and Gynaecology of the British Empire 25: 231
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MAIN STAGES OF PARENT-OFFSPRING CONFLICT: Survival of conceptus (2) Growth in the womb (3) Survival at birth - infanticide and baby fatness, cuteness (4) Investment in childhood - lactational amenorrhea, weaning, tantrums, language, learning (5) Inheritance as adult
Slide 17-

How parent-offspring conflicts contribute to disease Disruption of ‘tugs-of-war’ over resources (mild gestational diabetes or preclampsia leads to a bigger, fatter baby but severe cases endanger the life of both mother and fetus) (2) Wastes of resources (release of compounds by placenta that are ‘ignored’ by mother - hormonal ‘shouting’) (3) Maladaptations in party that ‘loses’ in a conflict - (mother ‘stuck’ with pregnancy, fetus takes fatty acids direct from mom’s brain, fetus controls parturition time) (4) Within-family ongoing verbal, physical conflicts and psychological health and well-being
Slide 18-

Genomic Conflicts, Health and Disease (1) What are genomic conflicts and how are they involved in disease? (2) Main forms of genomic conflict (a) Parent-offspring conflict (b) Genomic-imprinting conflict What is genomic imprinting and why has it evolved? Expression of a gene depending on whether inherited from father or mother Main arenas of imprinting effects on human health: -Placenta -Brain -Carcinogenesis -Stem cells -In vitro fertilization from dad from mom
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Imprinted gene expression compared to biallelic gene expression
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How imprinting works, across the life cycle
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Asymmetries in parental investment are high the mother alone gestates and lactates all her children have 50% of her genes the father contributes only a single sperm mixed paternity is common across births or broods Why imprinting has evolved, in placental mammals:
Slide 22-

Evolution of genomic imprinting in placental mammals under multiple paternity and high maternal investment: Paternal gene Maternal gene Relatedness of paternal gene in offspring, to siblings, goes from 0.5 to 0 as we go from monogamy to polygamy Relatedness of maternal gene in offspring, to siblings, is always 0.5 Paternally-expressed genes are expected to be more ‘selfish’, with regard to mother-offspring interactions
Slide 23-

Evolution of genomic imprinting in placental mammals under multiple paternity and high maternal investment: Paternal gene Maternal gene Relatedness of paternal gene in offspring, to siblings, goes from 0.5 to 0 as we go from monogamy to polygamy EXTREME CASE: Relatedness of maternal gene in offspring, to siblings, is always 0.5 Mum’s Brood
Slide 24-

IMPRINTED GENES Silenced (‘imprinted’) when inherited from either the father or the mother (-> parent of origin effects) (2) Paternally-expressed (maternally-silenced) genes are expected to be associated with increased demands on the mother, by offspring (3) Maternally-expressed genes are expected to be associated with reduced demands on the mother ‘TUGS-OF-WAR’ can result (eg IGF-II/IGF-IIR in pregnancy)
Slide 25-

EXAMPLE: TUG-OF-WAR over fetal growth in pregnancy In fetus: IGF-II paternally expressed, IGF-IIR maternally expressed Paternally-expressed gene generates IGF-II, Maternally-expressed gene IGF-IIR serves as non-functional ‘sink’ that degrades IGF-II WITHIN A Fetal Mouse:
Slide 26-

Imprinted genes are ‘master regulators’ of placentation: they control growth and differentiation
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CONFLICT THEORY OF IMPRINTING -> abundant support from empirical studies of imprinted genes and growth, in mice and humans IGF2-IGF2R (Haig & Graham 1991 Cell) (2) CDKN1C (Andrews et al. 2007 BMC Dev Biol) (3) GRB10 (Charalambous et al. 2003 PNAS) Beckwith- Wiedemann Syndrome Silver- Russell syndrome Mighty mouse Normal sized human 2 doses IGF2 1 dose IGF2 0 doses IGF2
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Effects of alterations to imprinted genes on the placenta in mice KNOCKOUTS
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*
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Dysregulation of imprinted genes in the placenta is an important cause of intra-uterine growth restriction (IUGR) in humans Imprinting Placentation
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Imprinting can cause genetic disorders, if both chromosomes are inherited from same parent
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About 100 imprinted genes are known, many more are predicted or apparent (need validation) Primary site of imprinted-gene expression is the (‘social’) placenta, which mediates the transfer of resources between mother and child Small deviations in placental function can benefit the child, or the mother Large deviations are costly to both The second-most important site of imprinted gene expression is the (‘social’) brain IMPRINTED GENE EXPRESSION IN THE PLACENTA AND IN THE BRAIN
Slide 34-

Imprinting & the brain ‘most imprinted genes will affect how much an offspring receives from its mother, at the expense of sibs. Thus imprinting is expected at loci that influence placental growth, suckling, neonatal behavior, appetite, nutrient metabolism and postnatal growth rate… it is worth considering the possibility that imprinting influences appetite control and hypothalamic function.’ After the placenta, genes are most-commonly imprinted in the brain
Slide 35-

Chimeric mouse brain
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The mother and the ‘maternal brain’ is the prime nurturer has equal number of genes in all her children (50%) her genes ‘build’ the part of the brain that can be nurtured and exercise restraint: the neo-cortex
Slide 37-

The father and the ‘paternal brain’ relies on his genes to control growth, development, and behaviour other children in the family need not share his genes his genes ‘build’ the limbic brain
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Paternally-expressed imprinted genes are especially commonly expressed in the hypothalamus, where they affect energy metabolism and other fundamental body functions (food, activity level, sex, sleep)
Slide 39-

Oppositely-imprinted disorders of the brain: Prader-Willi & Angelman syndromes Angelman: paternal additions and/or maternal deletions on chromosome 15q11-13 Prader-Willi: maternal additions and/or paternal deletions on chromosome 15q11-13
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Angelman Prader-Willi prolonged suckling frequent crying hyper-active/sleepless low pleasure threshold severe retardation: no language autism poor suckling weak crying inactive/sleepy high pain threshold affective psychosis in adults Complacent, easy on mom Every mother’s worst fear, as regards behaviour of a child
Slide 41-

b) Genomic-imprinting conflict What is genomic imprinting and why has it evolved? Expression of a gene depending on whether inherited from father or mother Main arenas of imprinting effects on human health: -Placenta -Brain -Carcinogenesis -Stem cells -In vitro fertilization
Slide 42-

Imprinting and Cancer: Paternally-expressed imprinted genes enhance growth/proliferation; some are ‘oncogenes’ Maternally-expressed Imprinted genes constrain growth/proliferation; some are ‘tumor suppressors’ PNAS, 2003
Slide 43-

Main mechanisms whereby alterations to imprinted genes promote cancer development
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Slide 45-

BWS = Beckwith- Wiedemann syndrome
Slide 46-

Alterations to genomic imprinting alter the properties of embryonic stem cells
Slide 47-

Genomic Conflicts, Health and Disease What are genomic conflicts and how are they involved in disease? (2) Main forms of genomic conflict (a) Parent-offspring conflict (b) Genomic-imprinting conflict (c) Sexual conflicts
Slide 48-

What is sexual conflict? Leigh Simmons Stems ultimately from differential investment by males and females in reproduction (e.g. anisogamy) Can lead to different optima in males and females for reproductive traits Reinforced by - multiple breeding episodes with different partners (low shared interest in future reproductive bouts) - low relatedness of mating pairs (usually 0) trait value fitness females males  Both optima cannot simultaneously be realised = sexual conflict
Slide 49-

Selection for adaptations that favour each sex reaching its optimum, despite the reduction in fitness this necessarily causes in the other sex Followed by counter adaptation for ‘resistance’ => sexually antagonistic coevolution Sexual conflict
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T. Chapman 2006, Curr. Biol. Relevence to human health?
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Think about these concepts when you think about sexual conflict
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Internal Male Reproductive System One arena of conflict: male ejaculate chemicals T T AG AG
Slide 53-

SIMPLE PEPTIDES (<100 a/a) HORMONE-LIKE (200-400 a/a) LARGE GLYCOPROTEINS (>400 a/a) Accessory gland proteins (Acps) Accessory glands
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Specific Acps: increase egg production decrease female receptivity after mating stimulate feeding essential for sperm storage process other Acps form a mating plug Several Acps: increase success in sperm competition have antibacterial activity Effects of Acps
Slide 55-

Acps increase egg laying, sperm storage, success in sperm competition, and temporarily prevent females from mating again in toto they act to increase male paternity, and therefore benefit males Acps benefit males
Slide 56-

but Acps can reduce female fitness ------ Full Acps ------ No Acps  Non-mating control (1)  Non-mating control (2) (Chapman et al 1995)
Slide 57-

At least 11% of Acps evolve rapidly e.g. Acp26Aa is fastest evolving gene in melanogaster genome (Ka/Ks ratios >1) Significant polymorphism AND divergence Also rapid evolution in female D. melanogaster reproductive tract proteins Lack of homologues, even between close relatives Recent evolution of Acp genes and high Acp gene turnover Rapid evolution in reproductive proteins
Slide 58-

Acps’s in humans: the prostate Unique to mammals, analogous to accessory glands in Drosophila Function is production of seminal fluid Consists of 30-50 sac-like glands connected to excretory ducts Secretions play key roles in the fertilizing abilities of the spermatozoa in the female reproductive tract
Slide 59-

Prostate functional design and evolution are essentially unstudied Is prostate size or form related to mating system, among primates and other animals, or among human races? What are the functions of the various compounds secreted by the prostate and seminal vesicles? Roles in human fertility, health?
Slide 60-

Growth, Differentiation and Human Sexual Dimorphism Mediated by androgens The main circulating androgen is testosterone (produced by Leydig cells of the testis) Testosterone + 5α Reductase (enzyme)  Dihydrotestosterone (DHT) This enzyme is specific to the prostate and liver * Androgens increase cell proliferation and inhibit apoptosis
Slide 61-

Role of DHT in the Prostate Binds to androgen-receptor proteins Gets transported into the nucleus Initiates transcription of androgen dependent genes Hence DHT controls the expression of many proteins of the seminal fluid
Slide 62-

Peptides and Proteins in Human Semen Heaps and heaps of compounds of unknown function, plus some known ones PSA = Prostate Specific Antigen A biomarker for prostate cancer Protects the sperm of it’s male and slows the sperm of others Semenogelin Two types (I and II) I- inhibits sperm motility and capacitation Both involved in the human semen coagulum Function in sperm competition in primates, evolves faster in primate species with multiple mating known ones hCG human chorionic gonadotropin !
Slide 63-

Evidence for adaptation in primate seminal proteins - though evidence of function is sparse
Slide 64-

Acps=accessory proteins (made in accessory glands) protein in Drosophila seminal fluids EFFECTS ON THE FEMALE in flies; what about in humans- effects on male and female? Increase -oogenesis -egg hatchability -sperm storage -ovulation Decrease -receptivity to remating -postmating viability -sperm loss -remating physically (are a component of the mating plug)
Slide 65-

Prostate Cancer Involves a series of sequential mutations Mutations inhibit apoptosis and drive cell proliferation Is testosterone-dependent (at least initially); breast cancer is often estrogen-dependent Progression is mediated by genetic variation in the androgen receptor gene Killer # 2 after lung cancer, surgery causes impotence and incontinence Most men get it if they live long enough; starts to develop in 20s - WHY?
Slide 66-

Hypothesis for the evolution of prostate cancer risk Strong selection for compounds that enhance male reproductive function, even at a cost to females, and a cost to males, especially in terms of cancer risk * Seminal proteins evolve under sexual conflict - antagonistic coevolution between genome as expressed in males and genome as expressed in females - predicted to show expression patterns associated with cancer -> directly analogous to costs of Acp’s in flies -> one key gene involved in prostate function, and prostate cancer risk, is the androgen receptor
Slide 67-

Androgen Receptor: protein that ‘activates’ effects of testosterone. Extent of activation is mediated by number of CAG microsatellite repeats MALES Lower number of repeats - increased activation of receptor and increased male fertility, but increased risk of prostate cancer Expect selection on males for fewer repeats (to a point) FEMALES Lower number of repeats, higher rates of breast cancer This is Evidence for Sexual Conflict
Slide 68-

What about other prostate-expressed genes - does their expression, activity affect cancer risk?
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Main ways that sexual conflicts may be involved in disease: Disruption of dynamic ‘tugs of war’ between parties in conflict over reproductive resources (as in parent - offspring, maternal genes-paternal genes, and males - females) (IGF2-IGF2R in pregnancy) (2) One party may ‘win’ a conflict, with costs imposed on the other party (hCG? androgen receptor?) (3) Strong selection and rapid evolution can result in maladaptive byproducts, whereby strong selection for one trait can result in maladaptation regarding other traits (seminal proteins? androgen receptor?) (4) Ongoing more or less direct physical, psychological conflicts, costly to one or both parties