Jones - reading Flashcards

(45 cards)

1
Q

What is fitness?

A

Survivors selected by ability to reproduce

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2
Q

What is the gene pool constantly doing?

A

Adapting

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3
Q

What is the purpose of reproduction?

A

Pass genes to next generation

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4
Q

How do most organisms reproduce?

A

asexually

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5
Q

How do unicellular organisms reproduce?

A

mitotically - produce two identical offspring

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6
Q

how do complex vertebrates reproduce?

A

Partenogenesis - egg cell doesn’t need sperm to become an embryo

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7
Q

How do mammals reproduce?

A

sexually

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8
Q

what is produced at fertilisation?

A

zygote

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9
Q

what is the function of meiosis?

A

halves genetic material

produces germ cells

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10
Q

How do mammals increase genetic diversity?

A

exchanging pieces of homologous chromosomes

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11
Q

What is a mechanism of recognising fitness in mammals?

A

sexual selection

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12
Q

Negatives of sexual selection

A

Energy expenditure in finding, attracting and keeping a partner
exposure of both partners to death

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13
Q

Why do mammals reproduce by internal fertilisation?

A

Reduced number of eggs - energy expenditure

women undergo egg loss but mainly before egg growth

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14
Q

What is viviparity?

A

production of smaller eggs
development in vivo
birthing live young

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15
Q

Positives of viiparity?

A

reduces pressure to develop quickly

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16
Q

negatives of viviparity?

A

long gestation is demanding on females

there is a selective pressure on birthing as it can go wrong

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17
Q

How long do mammals display parental care for?

A

An extended period

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18
Q

What is fercundity?

A

reproductive capacity

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19
Q

How does fercundity differ in males and females?

A

Males - persists throughout life, slowly declines

Females - declines steeply at 35, ends at 50, due to loss of egg quality

20
Q

Male contraception using testosterone levels

A

High testosterone leads to FSH stimulating spermatogenesis
could suppress endogenous testosterone production and therefore spermatogenesis
Shown as effective in some people - less in others
took a long time to get a low sperm count in some people

21
Q

Male contraception using small molecule inhibitors of BRDT

A

BRDT= testes specific epigenetic reader protein
JQ1 = BRDT inhibitor - targets bromodomain and prevents recognition of acetylated H4
reduces sperm number and motility without altering hormones
reversible withing 1 month

22
Q

Male contraception PLC3

A

Potential to inhibit PLC3 and prevent oocyte activation

no specific molecules found yet

23
Q

female contraception Target the zona pellucida

A

immuniation of zona pellucida

this may cause abnormal cycles

24
Q

Male contraception

Binding to the androgen and progesterone receptors

A

reduces testosterone conc in blood
effective and reversible
no serious side effects
weight gain

25
Male contraception | Adjudin
disrupts spermatid adhesion to sertoli cells | premature spermiation - not mature enough to fertilise
26
Male contraception | Retinoic acid receptor antagonists
Aldehyde dehydrogenase in setoli cells synthesises retanoic acid this is required for spermatageneis
27
Male contraception | Synthetic androgens
Supress gonadorophins and sperm production reversible may be incomplete suppression
28
Male contraception | Nestorone and testosterone gel
Progestin compound blocks testosterone production and reduces sperm production targets sertoli germ cell adhesion or sperm motility
29
Male contraception | Vasalgel
Reversibly blocks vas deferens prevents passage of sperm impairs sperm function reversible
30
Male contraception | Block to sperm delivery
100% efficacy after 15 days attaches to cells in vas deferens and blocks sperm passage leads to morpholically different sperm
31
Female contraception | Combined pill
Supresses secretion of progestogen and estrogen prevents ovulation as no LH surge inhibition of follicle maturation
32
Female contraception | Mini pill
progesterone only estetrol - produced during pregnancy less side effects
33
Femal contraception | Vaginal rings
Release haormones to prevent follicle development and ovuation does not need an trained proffessional but is longer lasting
34
female contraception | emergancy contraception
same hormones as normal pill delays ovulation needs to be 1 day befor LH surge - sometimes too late needs to be taken within 24 hours
35
IUDs
Copper or hormonal
36
Implants
Long lasting | hormonal
37
Injections
hormonal
38
new female contraception
COX2 inhibitors: less prostaglandin production and failure to ovulate Rofecoxib: delayed follicle rupture Meloxicam: interfers with ovulation
39
Are developmental abnormalities | more likely in babies generated via ART?
``` Different types of ART: do they all have the same level of risk?  Cancer risk?  Vitrification  ICSI vs IVF?  Imprinting disorders  Cardiometabolic problems  Low birth weight  Urogenital issues ```
40
Why are the results from different studies at odds | with one another?
 Underlying infertility/subfertility  Multiple births  Confounding variables e.g. maternal age, follow-up (closer scrutiny following ART), genetic origin, sample size  Differences in procedures over time and in different places (e.g. types of medication; day of transfer; oocyte/sperm selection criteria/culture media)  Risk behaviours (smoking, alcohol)  Importance of long-term follow-up
41
Are developmental abnormalities more likely in babies generated via ART? conclusion
The risks do seem to be slightly higher for some conditions.  BUT, don’t forget that these ART procedures result in the birth of thousands/millions of healthy (and desperately wanted) babies.  Additionally, the techniques are constantly being monitored, adapted and improved.
42
What methods are used to create ‘three-parent babies’? How do they work?
Cytoplasmic (ooplasmic transfer)  Mitochondrial replacement therapy (MRT) via Spindle transfer (ST) or Pronuclear transfer (PNT or PT)  Could also consider standard Nuclear Transfer
43
Are the techniques safe and effective?
ST appears safe in monkeys 33% effective - better than current rate no detectable heteroplasmy later study on humans showed abnormal separation of the second polar body
44
What are the benefits?
Couples able to conceive via CT despite poor-quality oocytes |  Couples able to conceive via ST and PNT despite maternal mtDNA disease
45
What problems can arise in offspring/future generations?
MtDNA heteroplasmy/persistence of donor or mutant mtDNA  Reversion of mtDNA population due to genetic drift  Developmental abnormalities