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Sexual dimorphism
Biological differences between males and females in body size, composition, behavior, hormonal profiles, and disease transmission routes, generated by selection for reproduction
Sex bias in medical research
Strong historical bias toward studying males while treating females as "anomalies," leading to lack of understanding of disease manifestation and medication responses in women
Intralocus sexual conflict
When natural and sexual selection favor different fitness optima in each sex, with genes favored in one sex being detrimental when expressed in the other due to shared genome
Genomic tug-of-war
The consequence of imperfect sex-specific gene expression in intralocus sexual conflict, where genes cannot be optimized for both sexes simultaneously
Cryptic female choice
Female mechanism in lizards where sperm from large males are directed to fertilize male offspring while sperm from small males fertilize female offspring, resolving intralocus conflict over body size
Parent-offspring genetic conflict
Conflict between paternal and maternal genes over fetal growth and resource allocation during pregnancy, where paternal genes encourage growth and maternal genes moderate it
Placental invasion
Process where placental tissue invades maternal uterine arteries, reducing arterial plasticity and promoting blood supply to the placenta, can lead to preeclampsia
Gestational diabetes
Condition during pregnancy where insulin resistance occurs due to placental hormones affecting maternal insulin sensitivity, with pancreas unable to produce sufficient insulin
Preeclampsia
High blood pressure condition in pregnancy resulting from placental tissue invasion of uterine arteries; can be early-onset (inadequate invasion) or late-onset (maternal cardiovascular defects)
Genomic imprinting
Epigenetic modification of genes dependent on parental heritage, where DNA sequence unchanged but chemical modification (methylation) silences one allele based on parent of origin
Imprinted genes
Genes where only one allele is expressed; which allele depends on whether it was inherited from mother or father
Methylation
Chemical modification where methyl groups attach to DNA segments, controlling whether DNA can be expressed; mechanism of genomic imprinting
Genetic conflict hypothesis (imprinting)
Theory that genomic imprinting evolved due to competition between male and female parents for maternal resources during pregnancy
Paternal imprinting
When genes inherited from father are silenced by methylation, typically promoting growth; opposite of maternal imprinting
Maternal imprinting
When genes inherited from mother are silenced by methylation, typically suppressing growth; opposite of paternal imprinting
Selfish genetic elements
Stretches of genome that gain increased transmission relative to rest of genome but are selectively neutral or detrimental to organismal fitness
Intragenomic conflict
Conflict within a genome where genes or stretches of DNA function to increase their own transmission at the detriment of other genes in the same genome
Genetic drive
When a genetic element is transmitted at higher rates to progeny than expected by Mendelian inheritance (not 50:50)
Transposable elements
DNA sequences able to move to new positions in the genome via cut-and-paste mechanism; among most successful selfish genetic elements; 45% of human genome
Biased gene converters
Selfish genetic elements that preferentially insert into homologous uninserted sites using homing endonucleases; likely originated from DNA repair processes
Meiotic drivers
Selfish genetic elements achieving drive through preferential segregation to functional gamete (egg in females) during gametogenesis
Gamete killers
Selfish genetic elements that selectively eliminate or disrupt gametes lacking the driving element, increasing transmission
B chromosomes
Additional chromosome sets not required for viability or fertility but persist in population via self-propagation; occur in 15% of eukaryotes
Selfish mitochondria
Maternal-inherited mitochondria in conflict with biparentally-inherited nuclear genes; example: cytoplasmic male sterility
Cytoplasmic male sterility
Loss of male fertility in hermaphroditic plants due to selfish mitochondria affecting resource allocation to female reproductive functions
Restorer genes
Nuclear genes evolved to suppress effects of cytoplasmic male sterility genes, creating evolutionary arms race
Two rules of selfish genetic elements (Rule 1)
Spread of SGEs requires sex and outbreeding; sexual reproduction places SGEs in new genomes; inbreeding reduces spread via decreased heterozygosity
Two rules of selfish genetic elements (Rule 2)
Presence of SGEs revealed in hybrids not population crosses; SGEs reach fixation rapidly; hybrids inherit SGE without suppressors, revealing phenotypic effects
Gonotaxis
Movement of genetic elements preferentially toward germline away from somatic cells; example mechanism of genetic drive
Segregation distorters
Selfish genetic elements using gonotaxis; example: maize chromosome knobs that pull themselves along spindle during female meiosis
P element (Drosophila)
Transposable element that causes reproductive isolation; males with P element crossed to females without show reduced fitness offspring
Interlocus sexual conflict
When male adaptation increasing sexual selection success simultaneously reduces female lifetime fecundity, with females evolving counter-adaptations
Sexually antagonistic coevolution
Perpetual evolutionary arms race between male traits harming females and female counter-adaptations, driven by interlocus sexual conflict
Sexual cannibalism
Predation of one sex during or after mating; is sexual conflict only if cannibalized sex loses fitness through lost future reproduction, not if benefits outweigh future opportunities
Male infanticide
Male strategy of killing offspring to induce female receptivity; occurs in lions and some spiders to increase paternity certainty
Cryptic female choice (in conflict context)
Female mechanism to allocate sperm and choose paternity allocation to counteract male-imposed harm
Sperm-egg interactions
Fast-evolving gamete recognition system where sperm less choosy than egg due to hybrid fitness potential and sperm competition in external fertilizers
Wolbachia
Common intracellular bacterium infecting approximately 2/3 of world's arthropods; transmitted maternally only via egg infection
Cytoplasmic incompatibility (Wolbachia)
Reproductive-manipulating mechanism where infected males can only reproduce with infected females; uninfected females produce early embryonic death
Wolbachia pest control
Strategy using cytoplasmic incompatibility to suppress arthropod pest populations; example: Asian tiger mosquito control with 200M released males achieving 94% reduction
Genome size variation (C-value)
Extraordinary variation in genome size across species (7000-fold in animals, 24000-fold in plants), poorly correlated with gene number or organismal complexity; partly due to SGEs
Reproductive isolation
Evolutionary consequence of SGEs where coevolution between elements and suppressors creates incompatibilities preventing successful reproduction between populations
Transposon repression
Host mechanism to suppress transposable element activity using small RNAs and silencing pathways; co-evolves rapidly with transposon activity (Red Queen Hypothesis)
Hybrid incompatibility
Reduced fitness in offspring from crosses between populations due to mismatches between SGEs and their suppressors
Gene duplication (SGE consequence)
Transposons cause gene duplications allowing functional divergence since original gene remains active, releasing new duplicate from strong selection
Disruptive transposition
Harmful transposon insertion that disrupts critical gene function; has been linked to cancer and hemophilia in humans
Beneficial transposition
Rare cases where transposable element insertion creates adaptive trait; examples in Drosophila and dogs show adaptive evolution associated with TE insertions
Anisogamy
Difference in gamete size between sexes (large egg, small sperm), generating intrinsic parental investment conflict integral to sexual selection
NIH mandate (1993)
Federal requirement for inclusion of females and people from different ethnic/racial groups in medical research following historical exclusion
Human placental invasiveness
Humans have most invasive placentas of any mammal, correlating with increased prevalence of preeclampsia
T-Cell Lymphotrophic Virus Type 1
Virus more likely to progress to adult T-cell leukemia in Japanese men than women; transmission route (breastfeeding duration) explains differential outcomes
Epigenetic modification
Chemical alteration of DNA or chromatin structure without changing DNA sequence; basis of genomic imprinting
Germline reprogramming (imprinting)
Week 11: PGCs retain <10% methylation; Week 19: remethylation begins; resets imprinting tags each generation
Lion male infanticide
New males kill cubs to make females unreceptive for current offspring, inducing receptivity for the new male's offspring
Stegodyphus lineatus (spider)
Spiders where males steal ~33% of egg sacks, forcing females to remate and lay replacement clutches, increasing male fertilization probability
Genital morphology (sexual conflict)
Males evolving structures to harm females into terminal investment; females evolving protective traits (interlocus sexual conflict)
Seminal fluid proteins
Male-produced proteins that upregulate female egg-laying and suppress remating, but shorten female lifespan (interlocus sexual conflict example)
Drosophila P elements
Transposable elements causing reproductive isolation; phenotype revealed only in hybrids (males with P × females without show reduced fitness)
Maize centromere knobs
Segregation distorters where knobs on maize chromosomes act as centromeres during female meiosis, pulling themselves into egg
Stalk-eyed flies sex-ratio distorters
Males carrying distorters have reduced sperm competitiveness; long stalks indicate genetic suppressors; females preferentially mate with suppressor males to ensure both sons and daughters
Polyandry evolution (SGE-driven)
Female multiple mating increases when males carry selfish genetic elements, allowing females to avoid passing elements to offspring while maintaining sperm competition
Killer gene K (meiotic drive)
Gamete killer element selective for non-K bearing sperm, increasing K-bearing sperm fertilization probability
C-value paradox
Lack of correlation between genome size and gene number or organismal complexity; explained partly by variable SGE content across species
Homing endonucleases
Endonucleases used by biased gene converters to cleave specific DNA sequences and repair with their own copy; basis for CRISPR-Cas9 technology
CRISPR gene drive
Artificial homing endonuclease system using CRISPR to produce guide RNAs cutting target genes, with homologous flanking sequences allowing construct insertion
Infection of egg but not sperm (Wolbachia)
Wolbachia maternal transmission mechanism; infected egg cytoplasm passes bacteria to offspring while sperm lacks cytoplasmic transmission
Wolbachia feminization
Wolbachia effect of converting male embryos to females; reproductive manipulation mechanism
Wolbachia fecundity reduction
Wolbachia ability to reduce female fertility as part of reproduction-manipulating strategy
Dengue virus prevention (Wolbachia)
Wolbachia prevents Dengue virus replication inside host cells, providing disease control benefits beyond cytoplasmic incompatibility
Somatic and germ cell transmission (Wolbachia)
Wolbachia transmits through both somatic cells and germline, replicating as host cells replicate
Lion-tiger hybrids (imprinting)
Offspring phenotype depends on species of mother due to different imprinting patterns between species; demonstrates rapid evolution of imprinting
Calico cats (imprinting)
Example of parent-of-origin gene expression effects due to genomic imprinting and X-chromosome inactivation
Placental lactogen (hPL)
Placental hormone affecting maternal insulin sensitivity and glucose metabolism, contributing to gestational diabetes risk
Hormonal manipulation (seminal fluid)
Male seminal fluid proteins manipulate female physiology to increase egg-laying and prevent remating, reducing female lifespan
Pre-eclampsia early-onset
Occurs when placental invasion inadequate, causing placental stress and deprived blood flow; driven by fetal genes
Pre-eclampsia late-onset
Occurs after 34 weeks due to maternal cardiovascular defects and impaired detoxification of metabolic byproducts
Human hip width compromise
Example of intralocus sexual conflict solution where hip width is compromise between male and female optima
Fruit flies (intralocus conflict)
No genomic conflict in juveniles but conflict in adults; sex-specific gene expression becomes stage-specific
Lizard testosterone expression
Testosterone at sexual maturity alters size-related gene expression in males and females, resolving intralocus conflict over body size
Transposition rate (self-fertilizers)
Greater linkage disequilibrium in self-fertilizing organisms selects for reduced transposition rates due to SGE-host linkage
Antibiotic resistance plasmids
Beneficial selfish genetic elements in bacteria; plasmids carry antibiotic resistance genes providing survival advantage
Inversion sequences (t haplotype)
Structural feature of t haplotype in mice preventing linkage disruption with resistance allele; spans >1/3 of chromosome 17
T haplotype mice
Ancient (~3 million years) selfish genetic element killing sperm lacking it; t/t homozygotes die in utero; females avoid incompatible males
Hybrid sterility
Reproductive isolation mechanism resulting from SGE coevolution incompatibilities between populations or species
Sex determination (Wolbachia)
Some insects use parent-of-origin gene expression affecting sex determination, potentially arising from genomic imprinting
Kinship theory (insects)
Hypothesis explaining imprinting evolution in social insects where worker behavior influenced by maternal genes and haplodiploid relatedness
Transposon repeat sequences
Imprinted genes cluster in areas with transposon repeat sequences, suggesting transposons may be prerequisite for imprinting
Endosperm imprinting (plants)
Genomic imprinting occurs in plant embryo and endosperm (nourishing tissue) to control nutrient flow from mother to offspring
Plant embryo imprinting
Maternal inheritance in plants creates imprinting conflict similar to mammalian parent-offspring conflict
Transposon control (plants)
Imprinting may regulate transposon activity in gametes, with imprinted genes in transposon repeat areas
Sexual conflict
Conflict over evolutionary interests of males and females regarding survival and reproduction where optimal outcomes differ
Intralocus vs. interlocus sexual conflict
Intralocus occurs at same locus with shared genome effects; interlocus occurs at different interacting loci with sexually antagonistic coevolution
Negative genetic correlation
When selection for increased value in males leads to decreased value in females (and vice versa) due to intralocus conflict
Genome-wide demethylation
Early reprogramming phase where most methylation erased during germline development
Remethylation
Re-establishment of imprinting marks on specific genes during germline development (begins week 19 in humans)
Non-sequence-based inheritance
Inheritance through epigenetic mechanisms like methylation rather than DNA sequence changes
Imprinting required for mammals
Genomic imprinting is essential for normal mammalian development; showed to evolve 150 MYA
Imprinting domains
Clustered regions of genome containing multiple imprinted genes, suggesting coordinated regulation
Imprinted gene diseases
Diseases resulting from mutations in imprinted genes; recessive alleles expressed if dominant silenced; examples vary by imprinting pattern
Sex ratio distortion
Skewed offspring sex ratios resulting from meiotic drivers on sex chromosomes; can cause population extinction