Human Embryology 1 Flashcards

1
Q

What is the study of development?

A

-Study of fertilized egg (zygote) transformation into a multicellualr organisms made of many different cell types that differentiated from one single cell

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2
Q

Developments big question?

A

how generate variety of cells and how put them together into something that makes sense and provides speicifc functions

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3
Q

Questions asked in development?

A

1) how are cells made
2) how are diff cells generated from the zygote
3) how are emerging cells organized into organs
4) what controls their behavior?

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4
Q

What is cell growth and differentiation? What is it controlled by?

A
  • controlled behavior & expression of certain genes in specific cells that give us developmental diversity
  • controlled by gene expression
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5
Q

two chick embryos and neurocrest cells?

A

1) chick #1 embryo see neurocrest cells emerging from the spine and spreading down spinal column
2) chick #2 neurcrest cells staying right around midbrain

-demonstrares how diff cells can express differently in different organisms

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6
Q

Preformationism?

A
  • the preformed theory
  • theory that organisms develop from miniature versions of themselves ( sperm contains little human inside)
  • was form that grew bigger than recreated itself by magic (like Russian dolls)
  • heavily based on religious ideals
  • went away…ressurfaced in 17th cent
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7
Q

Epigenesis

A
  • progressive generation of structures “knitting a net”

- a generation of form, not created from what existed before

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8
Q

cell theory

A

1) all living organisms are made of cells
2) cells are the basic unit of life
3) new cells are formed by the division of preexisting cells

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9
Q

who came up with cell theory?

A

-shwann, schledien, remark, virchow

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10
Q

Lazzaro Spallanzani

A
  • showed both oocyte & sperm were necessary for initiating development of a new animal
  • suggested the sperm was fertilizing agent that initiated the developmental processes
  • did artificial insemination in frogs, and dogs
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11
Q

Heinrich Christian Pander

A
  • Discovered three germ layers of the embryo:
    1) Ectoderm
    2) Mesoderm
    3) Endoderm
  • Suggested interdependence (communication) for their differentiation
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12
Q

Three germ layers of the embryo:

A

1) Ectoderm
2) Mesoderm
3) Endoderm

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13
Q

Martin Heinrich Rathke

A

-involved in comparative embryology of frogs fish turtles, mammals

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14
Q

Karl Ern von Baer (1827)

A

1) saw first unfertilized human & mammalian egg
2) developed Pander’s germ layer theory; studied their fates during embryonic development
3) comparative embryology

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15
Q

Karl Ern von Baer discovered what about the get layers?

A

1) “cutaneous” layer (external layer) transformed into superficial epidermis &CNS
2) “muscular” layer (somites) formed muscles, skeleton and connective tissues

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16
Q

Etienne Saint Hilaire &Isidore Saint Hilaire

A

-father & son
-first studies of abnormal
development in 1818
-animal experiments designed to produce birth defects–>Teratology

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17
Q

Teratology

A

the scientific study of congenital abnormalities and abnormal formations.

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18
Q

Mendel laws? What scientist proved Mendel as correct?

A

Law of:

1) Segregation
2) Independent Assortment
3) Dominance
- mendels laws solidified by Hertwig, Beneden, Weismann, Fleming, & Strasburger

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19
Q

Oscar Hertwig

A
  • sperm and egg meet at fertilization

- Meiosis in sea urchin eggs in 1876

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20
Q

Van Beneden

A

chromosomes combine in meiosis, making gametes

-1883

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21
Q

Fleming, & Strasburger

A
  • nucleoplasm and cytoplasm.
  • new cell nuclei can only arise from the division of other cell nuclei
  • 1878-1894
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22
Q

August Weismann

A
  • germ (egg and sperm) cells and somatic (body) cells
  • genetic contribution made exclusively by germ cells
  • 1892
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23
Q

developmental genetics; who led by (x3)?

A

-1980s
-Systematic Analysis of genetic Mutations,
Phenotypes and Inheritance
1) Lewis
2)Nüsslein-Volhard
3) Wieschaus

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24
Q

what is development?

A

-an orderly succession of different cell behaviors

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25
Q

What is development dependent on?

A
  • a progressive series of instructions
  • a generative program that relies on a list of actions w/ each action built upon the previous action (can’t skip steps
  • Nodal Points
  • toolkit genes
26
Q

Nodal Points

A
  • integrate complex information and yield simple outputs

- 5 diff mechanisms that tell us we are thirsty, simple output is drinking water

27
Q

toolkit genes

A
  • recycling instructions
  • have functions of development that are reused multiple times for different purposes
  • often highly conserved across species
  • some involved w/ cancer or mutations
  • many are trxn factors
28
Q

How control genes that have multiple different in different tissues?

A
  • trxn factors
  • proteins that are expressed at speicifc times, are context dependent, and trxn only genes we need in the tissue we need
29
Q

Pax6

A
  • trxn factor, highly expressed in developing eye
  • the master regulator of eye development
  • essential in neural & Eye development
  • role in eye development is conserved in multiple model organisms and humans
30
Q

Pax6 conservation?

A
  • Pax6 sequence & function are highly conserved between species
  • flies & mice: mutant phenotype = absence of eyes
31
Q

Human Pax6?

A
  • heterozygous (most common): called aniridia (absence of irises)
  • homozygous: eyeless phenotype
32
Q

overview of human development (x4)

A

1) sperm + egg fuse (zygote)
2) produce identical pluripotent cells (can give rise to any cell types)
3) cells being to specialize/ differentiate
4) get a fetus w/ a variable combo of traits from both parents

33
Q

zygote

A
  • a eukaryotic cell formed by fertilization between two gametes.
  • zygote’s genome is a combo DNA in each gamete, contains all the genetic info to form a fetus
34
Q

Germ cells

A

-gonad Diploid
cells that produce
gametes (egg/sperm)

35
Q

Gametes

A
  • haploid

- sperms and eggs

36
Q

Zygote

A

-diploid
-fused sperm
& egg

37
Q

Somatic cells

A
  • diploid

- all other body cells

38
Q

Meiosis broad steps?

A

1) DNA replication
2) recombination
3) first meiotic division
4) second meiotic division

39
Q

Spermatogenesis

A
  • occurs in testes
    1) spermatogonia: have A0-A4 intermediate then B type cont. to next step
    2) primary spermocyte; undergo first meiotic divsion(4n; 46 chrom pairs)
    3) secondary spermocyte: 2n, 23 chrom pairs (first meiotic division complete); does 2nd meiotic divison
    4) spermatids: haploid (n); 23 chromosomes
    5) mature sperms haploid (2X; 2Y)
40
Q

sperm proliferation & maturation?

A

-lifelong in males, increases at puberty decreases with older age
-100 X10^6 viable
sperm daily

41
Q

Syncytium

A
  • single cell or cytoplasmic mass w/ several nuclei

- formed by fusion of cells or by division of nuclei.

42
Q

Spermatogenesis & syncytium?

A
  • spermaocytes arent seperated until reach mature sperm stage
  • undergo meiosis 1, 2 & make spermatid while still linked/together
  • shows differentiation occurs very late
43
Q

Gametogenesis & the testes process?

A
  • Gametogenesis occurs in seminiferous tubules in the
  • the premature sperms are distributed within the tubes according to maturation
    1) Spermatogonia: outside
    2) primary/secondary spermatocytes: closer inside
    3) mature sperm: in lumen w/ fluid that can transport it for ejaculation
44
Q

where is sperm produced? how store it and deliver it (ejaculate)?

A
  • made in seminiferous tubules of testis
  • moves into epididymis, where non-mobile sperm is stored, becomes mobile when ejaculate
  • moves up epididymus…past prostate & seminal glands then released to penis
45
Q

Epididymis

A
  • in adults 6-7ft long,
  • connects ducts from rear of each testicle to its vas deferens
  • stores non-motile sperm, which becomes motile in ejaculate
46
Q

vas deferens

A

the duct that conveys sperm from the testicle to the urethra

47
Q

Sperm structure?

A
  • large head w/ acrosome at tip that covers the nucleus
  • neck that connects to thick middle tail piece that contains mito
  • thin tail
  • thinner end piece of tail (flagellum)
  • all together= 5um
  • is very inefficient at getting shit done
48
Q

Oocyte structure?

A

-overall 75um

49
Q

how know when sperm is mature?

A

-when acrosome is mature, sperm is mature

50
Q

centrioles in sperm production?

A
  • are what flagellum grow from

- flagellum=microtubules

51
Q

Sperm genome?

A
  • sperm nuclei is 5um; human genome= 1.82m
  • means that the sperm genome has to be highly condensed chromatin, more so than even in normal nuclei since the sperm is so small
  • have to do a lot of epigenetic changes to fit everything in
52
Q

Sperm genome epigenetic changes?

A

-DNA methylation
-Replacement of standard histones w/ nucleo-protamines
(MOST histones replaced, few do remain)
-creation of toroidal chromatin subunits

53
Q

nucleo-protamines

A
  • are proteins that help compact sperm genome
  • replace most standard histones in sperm nuclei
  • bind DNA condensing spermatid genome (making genetically inactive)`
54
Q

toroidal chromatin subunits

A

-DNA coiled & condensed into these much larger, subunits

55
Q

Are histones retained in sperm nuclei?

A
  • Yes. ~10-15% of the sperm’s genome remain packaged by histones
  • is thought to be so that genes that endow proteins important for sperm maturity and early fertilization can still be trxn/active
  • other than this 10-15% the DNA is so compacted it is incredibly hard to trxn genes
56
Q

Normal Spermatozoon morphology?

A
  • Smooth, symmetric, oval nucleus
  • absence of vacuoles
  • Acrosome, post-acrosomal lamina
  • Neck and Tail
  • no cytoplasm around the head
57
Q

Oogenesis

A

-occurs in the ovary
1) primary oocyte underwent replication is 4n; in primary follicle
2) folilicle grows w/ primary oocyte still in it; begins meisois 1
3) secondary oocyte now has 2n (23 chrom pairs) . meisosis 1 completeled, polar body remains inside oocyte
^remains here until fertilization
4) fertilized oocyte, completes second meiotic division; second polar body is in the oocyte

58
Q

Do the polar bodies get expelled? when?

A

polar bodies not expelled, but do usually dissolve as oocyte becomes mature & fertilized

59
Q

oocytes in female body?

A

400,000 at birth; remain arrested as primary oocyte until puberty

  • then maturing one every 28 days after puberty
  • only complete meisosis 2 once fertilized
  • only ~400 ovulated
  • women thought to not make more eggs once born
60
Q

Argument against claim that can’t make more stem cells once born?

A
  • presence of oocyte stem cells in ovaries
  • argument that the newly prorudced eggs are the ones being used and contributing to oocytes
  • suggested by Jonathan Tilly