The Questions of Developmental Biology

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Formation of the Neural Tube There are two major ways of forming a neural tube. In primary neurulation, the cells surrounding the neural plate direct the neural plate cells to proliferate, invaginate, and pinch off from the surface to form a hollow tube. In secondary neurulation, the neural tube arises from a solid cord of cells that sinks into the embryo and subsequently hollows out (cavitates) to form a hollow tube. The extent to which these modes of construction are used varies among vertebrate classes. Neurulation in fishes is exclusively secondary. In birds, the anterior portions of the neural tube are constructed by primary neurulation, while the neural tube caudal to the twenty-seventh somite pair (i.e., everything posterior to the hindlimbs) is made by secondary neurulation (Pasteels 1937; Catala et al. 1996). In amphibians, such as Xenopus, most of the tadpole neural tube is made by primary neurulation, but the tail neural tube is derived from secondary neurulation (Gont et al. 1993). In mice (and probably humans, too), secondary neurulation begins at or around the level of somite 35 (Schoenwolf 1984; Nievelstein et al. 1993). Primary neurulation The events of primary neurulation in the chick and the frog are illustrated in Figures 12.3 and 12.4, respectively. During primary neurulation, the original ectoderm is divided into three sets of cells: (1) the internally positioned neural tube, which will form the brain and spinal cord, (2) the externally positioned epidermis of the skin, and (3) the neural crest cells. The neural crest cells form in the region that connects the neural tube and epidermis, but then migrate elsewhere; they will generate the peripheral neurons and glia, the pigment cells of the skin, and several other cell types. The process of primary neurulation appears to be similar in amphibians, reptiles, birds, and mammals (Gallera 1971). Shortly after the neural plate has formed, its edges thicken and move upward to form the neural folds, while a U-shaped neural groove appears in the center of the plate, dividing the future right and left sides of the embryo (see Figures 12.2C and 12.3). The neural folds migrate toward the midline of the embryo, eventually fusing to form the neural tube beneath the overlying ectoderm. The cells at the dorsalmost portion of the neural tube become the neural crest cells. Neurulation occurs in somewhat different ways in different regions of the body. The head, trunk, and tail each form their region of the neural tube in ways that reflect the inductive relationship of the pharyngeal endoderm, prechordal plate, and notochord to its overlying ectoderm (Chapters 10 and 11). The head and trunk regions both undergo variants of primary neurulation, and this process can be divided into four distinct but spatially and temporally overlapping stages: (1) formation of the neural plate; (2) shaping of the neural plate; (3) bending of the neural plate to form the neural groove; and (4) closure of the neural groove to form the neural tube (Smith and Schoenwolf 1997; see Figure 12.2). Formation and shaping of the neural plate. The process of neurulation begins when the underlying dorsal mesoderm (and pharyngeal endoderm in the head region) signals the ectodermal cells above it to elongate into columnar neural plate cells (Smith and Schoenwolf 1989; Keller et al. 1992 ). Their elongated shape distinguishes the cells of the prospective neural plate from the flatter pre-epidermal cells
surrounding them. As much as 50% of the ectoderm is included in the neural plate. The neural plate is shaped by the intrinsic movements of the epidermal and neural plate regions. Fig 12.3 The neural plate lengthens along the anterior-posterior axis, narrowing itself so that subsequent bending will form a tube (instead of a spherical capsule). In both amphibians and amniotes, the neural plate lengthens and narrows by convergent extension, intercalating several layers of cells into a few layers. In addition, the cell divisions of the neural plate cells are preferentially in the rostral-caudal (beak-tail; anterior-posterior) direction (Jacobson and Sater 1988; Schoenwolf and Alvarez 1989; Sausedo et al. 1997; see Figures 12.2 and 12.3). These events will occur even if the tissues involved are isolated.
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PART 1. Principles of development i
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PART 2: Early embryonic development
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15. Lateral plate mesoderm and endo
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Hox Genes: Descent with Modificatio
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The question of growth. How do our
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Embryonic homologies One of the mos
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absent (Figure 1.16A). Over 7000 af
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Such growth, in which the shape is
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One way to search for the chemicals
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2 3 hours as adults, and they must
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for the following spring's breeding
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VADE MECUM Amphibian development. T
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The formation of a cap is a complex
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In Chlamydomonas, recognition occur
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organism with two distinct and inte
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Aggregation is initiated as each of
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The mathematics of such oscillation
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gonidia to undergo a modified patte
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Sponges develop in a manner so diff
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Embryology provides an endless asso
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Environmental sex determination Sex
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Protection of the egg by sunscreens
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The Developmental Mechanics of Cell
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Autonomous specification was first
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In postulating this model, Weismann
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Insofar as it contains a nucleus, e
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Other tissues may use the same grad
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will give rise to its particular or
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Sydney Brenner (quoted in Wilkins 1
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The results of their experiments we
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This observation led Steinberg to p
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into a single layer of cells (Takei
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6. In conditional specification, th
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3. Geneticists had to explain pheno
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These events are not the normal rou
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differentiated; each of them contai
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federal proscription of human cloni
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ecombinase enzymes are active only
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In situ hybridization But where was
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damaged.) The second primer is adde
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By using the appropriate restrictio
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These homozygous mutant mice lacked
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Phenotype Manipulation This technol
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The second approach is candidate ge
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developmental genetics is different
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This gene consists of the following
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In addition to these basal transcri
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Enhancers are critical in the regul
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The third functional region of MITF
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A fourth enhancer sequence, located
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The discovery of the human globin L
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The results of this procedure are o
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In vertebrates, the presence of met
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chromatin that remains condensed th
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Second, knocking out one Xist locus
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types of cells (Kleene and Humphrey
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(Sxl) gene,* while the autosomes pr
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Table 5.3. Some mRNAs stored in ooc
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determine the anterior-posterior ax
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6. Cell-cell communication in devel
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The inducing tissue does not need i
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Instructive and permissive interact
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mouth, whereas the frog tadpole pro
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are utilized throughout the animal
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includes the TGF-β family, the act
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The RTK spans the cell membrane, an
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members of this family: the C. eleg
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The Wnt pathway Members of the Wnt
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The Hedgehog pathway is extremely i
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A series of mutations has been foun
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The Nature of Human Syndromes As we
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vertebral column deformities, myopi
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The mammalian homologue of CED-4 is
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In the absence of Notch gene transc
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extracellular matrix (Figure 6.32).
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mammary gland tissue. The binding o
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In some cells, gene transcription r
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PARTE 2. Early embryonic developmen
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The means by which sperm are propel
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The sperm released during ejaculati
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Lying immediately beneath the plasm
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The mechanisms of chemotaxis differ
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Once the sea urchin sperm has penet
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Removal of these threonine- or seri
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undergo the acrosomal reaction with
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Gamete Fusion and the Prevention of
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The fast block to polyspermy. The f
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envelope to expand and become the f
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The calcium ions responsible for th
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Thus, the conversion of NAD + to NA
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eticulum (McPherson et al. 1992). T
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cAMP-dependent protein kinase activ
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These cells divide to form embryos
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(Figure 7.34; Elinson and Rowning 1
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6. In many species, eggs secrete di
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One consequence of this rapid cell
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Table 8.1. Karyokinesis and cytokin
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provides a classification of cleava
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This occurred at precisely the time
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These rapid and invariant cell clea
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The identities of the signaling mol
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Ingression of primary mesenchyme Fu
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But these guidance cues cannot be s
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lastocoel wall (Dan and Okazaki 195
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The orientation of the cleavage pla
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stage, the remaining cells divide n
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embryos can produce these cells, bu
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Early Development in Tunicates Tuni
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(or inactivating) specific genes. T
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occur under laboratory conditions.
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the germ cells. Using fluorescent a
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Conditional specification As we saw
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eggs. Coda This chapter has describ
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9. The genetics of axis specificati
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Following cycle 13, the oocyte plas
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Thus, at the end of germ band forma
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Classic embryological experiments d
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posterior region of the unfertilize
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Further studies have strengthened t
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The Hunchback protein also works wi
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transcription factor to activate an
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The gap genes The gap genes were or
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Table 9.2. Major genes affecting se
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The development of the normal patte
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However, the mechanism by which the
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As we saw above, the gap gene and p
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can substitute for Ultrabithorax an
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The Translocation of Dorsal Protein
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The Gurken signal is received by th
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This fate map is generated by the g
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first glimpses of the multiple leve
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10. Early development and axis form
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While these cells are dividing, num
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The next phase of gastrulation invo
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Black and Gerhart (1985, 1986) let
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The convergent extension of the dor
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During early gastrulation, three ro
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Spemann concluded from this experim
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Hans Spemann and Hilde Mangold: Pri
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We will take up each of these quest
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Moreover, the injection of exogenou
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Page 297 and 298: 11. The early development of verteb
Page 299 and 300: Gastrulation in Fish Embryos The fi
Page 301 and 302: If one conceptually opens a Xenopus
Page 303 and 304: Left-right axis formation Little is
Page 305 and 306: thereby forming the secondary hypob
Page 307 and 308: This region, the germinal crescent,
Page 309 and 310: Axis Formation in the Chick Embryo
Page 311 and 312: The mechanisms for neural induction
Page 313 and 314: *Arendt and Nübler-Jung (1999) hav
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Page 317 and 318: Modifications for development withi
Page 319 and 320: The ectodermal precursors end up an
Page 321 and 322: These include the genes for transcr
Page 323 and 324: Experimental analysis of the hox co
Page 325 and 326: Kessel and Gruss (1991) found this
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Page 329 and 330: 7. In birds, gravity is critical in
Page 331 and 332: This tissue forms the amnionic sac
Page 333: 12. The central nervous system and
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Page 339 and 340: Fig 12.6 Human neural tube closure
Page 341 and 342: The anterior-posterior axis The ear
Page 343 and 344: Ventral patterning of the neural tu
Page 345 and 346: The time of this vertical division
Page 347 and 348: layer (Wallace 1999). Each Purkinje
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Page 351 and 352: Neuronal Types The human brain cons
Page 353 and 354: Neurons transmit electrical impulse
Page 355 and 356: Development of the Vertebrate Eye A
Page 357 and 358: In addition, there are numerous Mü
Page 359 and 360: are shed and are replaced by new ce
Page 361 and 362: Just as there is a pluripotent neur
Page 363 and 364: 13. Neural crest cells and axonal s
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Page 367 and 368: Recognition of surrounding extracel
Page 369 and 370: However, D. J. Anderson's laborator
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Page 375 and 376: Soon afterward, the expression patt
Page 377 and 378: Ericson and colleagues (1996) have
Page 379 and 380: That it must be a sort of a surface
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Page 383 and 384: Guidance by diffusible molecules Ne
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There is some reciprocity in scienc
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The activity of the synapse release
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Growth of the retinal ganglion axon
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The complicated nerve fiber circuit
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Snapshot Summary: Neural Crest Cell
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Fetal Neurons in Adult Hosts In 197
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Somites give rise to the cells that
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Eph signaling is thought to mediate
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(The dermis of other areas of the b
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Muscle cell fusion The myotome cell
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The mechanism of intramembranous os
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mitochondrial energy potential (Sha
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Mutations in FGFR1 can cause Pfeiff
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These buds eventually separate from
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Step 2: The metanephrogenic mesench
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Step 5: Conversion of the aggregate
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6. The two myotome regions are spec
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The Heart The circulatory system is
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This fusion occurs at about 29 hour
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Formation of Blood Vessels Although
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networks of each organ arise within
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In some instances, angiogenesis may
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This became apparent when experimen
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Blood and lymphocyte lineages. Figu
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Chick cells are readily distinguish
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In mammalian embryos, food and oxyg
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*In some infants, the septa fail to
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As Figure 15.27 shows, the stomach
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The surfactant enables the alveolar
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In mammals, the size of the allanto
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inhibits liver formation (Figure 15
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Moreover, as will be detailed in Ch
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These cells secrete the paracrine f
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Induction of the apical ectodermal
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The progress zone: The mesodermal c
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The mechanism by which Hox genes co
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Thus, while the Hox gene expression
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Charité and colleagues (1994) have
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Between the time when the cell's de
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Snapshot Summary: The Tetrapod Limb
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This environmental view of sex dete
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The cells of the seminiferous tubul
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into the mesenchyme, but stay near
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There was a strict correlation betw
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Wnt4: a potential ovary-determining
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Anti-müllerian duct hormone Anti-M
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in another (see Jacklin 1981; Bleie
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Chromosomal Sex Determination in Dr
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The sex-lethal gene as the pivot fo
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Doublesex: The switch gene of sex d
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It is not known whether the tempera
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18. Metamorphosis, regeneration, an
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There are no ipsilateral (same-side
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Organ-specific response to thyroid
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The more T 3 receptors a tissue has
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Other species, such as A. tigrinum,
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Metamorphosis in Insects Types of i
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On one side of the sac, the epithel
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During the first larval instar, the
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central region producing the Wingle
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The molecular biology of hydroxyecd
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Since its discovery in 1954, when B
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How do they regain the ability to d
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It is probable that during normal r
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The head activator gradient. The ab
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*The tradition of leaving one's boo
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However, recent studies have indica
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Moreover, if a mutation occured in
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Snapshot Summary: Metamorphosis, Re
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19. The saga of the germ line We be
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In the nematode C. elegans, the ger
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When ultraviolet light is applied t
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Fibronectin is likely to be an impo
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Germ cell migration in birds and re
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EG Cells, ES Cells, and Teratocarci
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come together and are then separate
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The distal tip cell extends long fi
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The initiation of spermatogenesis d
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ecause the flagellum is beginning t
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A partial catalogue of the material
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When a specific 340-base sequence f
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Oocyte chromosomes can be incubated
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The structure of the meroistic ovar
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Periodically, a group of primordial
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Following ovulation, the luteal pha
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20. An overview of plant developmen
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oth the embryo and the mature sporo
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*A small weed in the mustard family
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should provide information on the e
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of hormones. In scarlet runner bean
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embryos demonstrate that isolated p
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When the shoot emerges from the soi
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etween nodes is called an internode
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flowering patterns among the over 3
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genes, class D genes are now being
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Table 21.1. Specific settlement sub
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Predictable Environmental Differenc
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Diapause Many species of insects ha
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The hindwing pigments of the short-
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Ferguson and Joanen (1982) speculat
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Predator-Induced Defenses One survi
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3. Antigens are presented (usually
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the ipsilateral eye. The situation
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*The importance of substrates for l
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Thus, most abnormal embryos are spo
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Retinoic acid as a teratogen In som
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Another pathway to apoptosis involv
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Whether heavy maternal alcohol cons
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Some scientists, however, say that
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Chains of causation Whether in law
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Snapshot Summary: The Environmental
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One could emphasize the common desc
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The search for the Urbilaterian anc
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Hox Genes: Descent with Modificatio
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Changes in Hox gene transcription p
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But within the crustacean lineages,
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Changes in Hox gene number The numb
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Homologous Pathways of Development
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The gradient of Dpp concentration f
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Modularity: The Prerequisite for Ev
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Such a trait would be selected for
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*The lack of such transitional form
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Coevolution of ligand and receptor
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Evidence for this mathematical mode
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It is difficult for a mutation to a
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The population genetics model conta
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However, once one adds development
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A partial list of genes active in h
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The Questions of Developmental Biology

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