Cell lineage analysis by intracellular injection of a tracer enzyme

Science ◽  
1978 ◽  
Vol 202 (4374) ◽  
pp. 1295-1298 ◽  
Author(s):  
D. Weisblat ◽  
R. Sawyer ◽  
G. Stent
Keyword(s):  
Cell Lineage ◽  
Intracellular Injection ◽  
Lineage Analysis

Fate mapping and cell lineage analysis of Hensen's node in the chick embryo

Development ◽  
1991 ◽  
Vol 112 (2) ◽  
pp. 615-626 ◽  
Author(s):  
M.A. Selleck ◽  
C.D. Stern
Keyword(s):  
Chick Embryo ◽  
Cell Lineage ◽  
Primitive Streak ◽  
Cell Types ◽  
Intracellular Injection ◽  
Anterior Midline ◽  
Stage 4 ◽  
Separate Region ◽  
Notochord Cells ◽  
Lineage Analysis

Fate maps of chick Hensen's node were generated using DiI and the lineage of individual cells studied by intracellular injection of lysine-rhodamine-dextran (LRD). The cell types contained within the node are organized both spatially and temporally. At the definitive primitive streak stage (Hamburger and Hamilton stage 4), Hensen's node contains presumptive notochord cells mainly in its anterior midline and presumptive somite cells in more lateral regions. Early in development it also contains presumptive endoderm cells. At all stages studied (stages 3–9), some individual cells contribute progeny to more than one of these tissues. The somitic precursors in Hensen's node only contribute to the medial halves of the somites. The lateral halves of the somites are derived from a separate region in the primitive streak, caudal to Hensen's node.

Cell lineage analysis by intracellular injection of fluorescent tracers

Science ◽  
1980 ◽  
Vol 209 (4464) ◽  
pp. 1538-1541 ◽  
Author(s):  
D. Weisblat ◽  
S. Zackson ◽  
S. Blair ◽  
J. Young
Keyword(s):  
Cell Lineage ◽  
Fluorescent Tracers ◽  
Intracellular Injection ◽  
Lineage Analysis

Major sex-determining genes and the control of sexual dimorphism in Caenorhabditis elegans

Genome ◽  
1989 ◽  
Vol 31 (2) ◽  
pp. 625-637 ◽  
Author(s):  
Jonathan Hodgkin ◽  
Andrew D. Chisholm ◽  
Michael M. Shen
Keyword(s):  
Caenorhabditis Elegans ◽  
Sex Determination ◽  
X Chromosome ◽  
Germ Line ◽  
Cell Lineage ◽  
Regulatory Genes ◽  
Nematode Caenorhabditis Elegans ◽  
X Chromosomes ◽  
The Many ◽  
Lineage Analysis

Sex determination in Caenorhabditis elegans involves a cascade of major regulatory genes connecting the primary sex determining signal, X chromosome dosage, to key switch genes, which in turn direct development along either male or female pathways. Animals with one X chromosome (XO) are male, while animals with two X chromosomes (XX) are hermaphrodite: hermaphrodite development occurs because the action of the regulatory genes is modified in the germ line so that both sperm and oocytes are made inside a completely female soma. The regulatory genes are being examined by both genetic and molecular means. We discuss how these major genes, in particular the last switch gene in the cascade, tra-1, might regulate the many different sex-specific events that occur during the development of the hermaphrodite and of the male.Key words: nematode, Caenorhabditis elegans, sex determination, sexual differentiation, cell lineage analysis.

Cell lineage of homeotic mutants of Drosophila

1985 ◽  
Vol 312 (1153) ◽  
pp. 139-144 ◽  
Keyword(s):  
Mode Of Action ◽  
Cell Lineage ◽  
Precursor Cells ◽  
Larval Period ◽  
Homeotic Genes ◽  
Lineage Analysis

The homeotic genes specify the development of specific groups of precursor cells. They establish the correct state of determination of the different primordia. Cell lineage analysis has been particularly useful in studying the mode of action of homeotic genes. The main findings are: (i) most, perhaps all, the homeotic genes are required by every cell of the corresponding primordium (that is, they are cell autonomous); (ii) they act on anatomical units defined by compartment boundaries and including one or more compartments, (iii) most, but not all, homeotic genes are required until the end of the larval period; (iv) the homeotic genes act in combination so that the appropriate development of a given primordium may be established by the contribution of several homeotic genes.

Cell lineage analysis in neural crest ontogeny

1993 ◽  
Vol 24 (2) ◽  
pp. 146-161 ◽  
Author(s):  
Nicole M. Le Douarin ◽  
Elisabeth Dupin
Keyword(s):  
Neural Crest ◽  
Cell Lineage ◽  
Lineage Analysis

Genetic analysis of leaf development in cotton

Development ◽  
1991 ◽  
Vol 113 (Supplement_1) ◽  
pp. 39-46 ◽  
Author(s):  
Liam Dolan ◽  
R. Scott Poethig
Keyword(s):  
Leaf Growth ◽  
Leaf Shape ◽  
Cell Lineage ◽  
Cotton Leaf ◽  
Expansion Phase ◽  
Genetic Mosaics ◽  
Developmental Age ◽  
Allometric Analysis ◽  
Marginal Region ◽  
Lineage Analysis

Leaf shape in cotton is regulated by the developmental age of the shoot and by several major genes that affect leaf lobing. The effect of these factors was investigated by allometric analysis, cell lineage analysis, and by studying the expression of the leaf shape mutation, Okra, in genetic mosaics. Allometric analysis of leaf growth suggests that leaf shape is determined during the initiation of the primordium rather than during the expansion phase of leaf growth. Clonal analysis demonstrates that both the rate and duration of cell division are fairly uniform throughout the leaf. Cells in the marginal region of the developing cotton leaf contribute more to the growth of the lamina than they do in tobacco. The Okra mutation acts early in the development of a leaf and appears to accentuate a developmental pattern that is also responsible for heteroblastic variation in leaf shape. The expression of this mutation in genetic mosaics demonstrates that its effect does not diffuse laterally within the leaf primordium.

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