Articles
Morphogenetic
Genes, Symmetric Variation, and the Production of Form in Drosophilia
By Anonymous
Many of the
main areas of development of form in the vinegar fly, Drosophila,
are now known. The main aspects of the production of form are controlled
by very special genes. One part of the egg chamber, in its early
stage, is divided into many nurse cells and the oocyte, or the unfertilized
egg, is in the other part of the chamber. There is a cytoplasmic
bridge by which the mRNA molecules cross over from the nurse cells
into the area of the oocyte. Cellular organelles and proteins also
make this journey from the nurse cell region to the oocyte. The
mRNA molecules help to restrict the expression and spatial distribution
of proteins (Gehring, 1998, p. 138). The head versus tail polarity
of the egg and beginnings of the embryo are dependent on this distribution
of mRNA in an asymmetrical fashion.
The distribution
of mRNA is caused by signals in the mRNA and on the RNA-binding
proteins that recognize such signals (Cost and Schedi, 2001, pp.
593-595). Mter about two or three days the Hox gene called Hedgehog
plays an early role by stimulating the change of ovarian somatic
cells into stem cells. Without hedgehog this cannot happen (Zhang
and Kalderson, ZOO I, pp. 599-604.
The polarity
of the oocyte is established as soon as some of the mRNA molecules
are translated into proteins. Bicoid is one such protein which helps
establish the head end. In fact, if you put this protein at both
ends, two heads result. RNA bicoid together with RNA's of two genes
called oskar and torso-like produce three pathways which give rise
to four protein gradients that start subdividing the embryo (N usslein-
Volhard, 1996, pp. 38-43). A gradient of another protein called
dpp actively subdivides the dorsal ectoderm of the Drosophila embryo
into two areas: amnioserosa and dorsal epidermis. The two proteins
called short gastrulation and tolloid help to shape this gradient
(Ashe and Levine, 1999, pp. 427-430.
The Hox gene
Hedgehog helps to initiate the formation of eyes and limbs (Brown,
200 I, pp. 48-49). Dpp also is seen as crucial for Drosophila wing
development (de Celis, Barrion and Kafatos, 1996, pp. 421-424.
The main aspects
of development are clearly caused by proteins and these proteins
remain stable because of the principle of symmetric variation (Brown,
1999, p. 200). Some changes in DNA chemical bases that ultimately
code for amino acids resulting in the proteins will produce the
same outcome, hence the term 'symmetric: Other DNA changes will
field amino acids within the same chemical group to which the original
amino acid belonged. If these remain, they can produce broader changes.
The enzyme repair system, however, will repair most of the changes
including many that would be adverse. For a review of how all this
works, see Brown, 1989, pp.I8-19. Changes therefore, in these proteins,
can bring about changes in form but such change is moderated by
symmetric variation and is thus always kept within the kind. We
will have far to go before we can express the same detailed understanding
of most life forms that is possible now with Drosophila, but what
we do know supports the belief that the Creator produces an animal's
form by means of a series of marvelous developmental genes. In one
such example of a recent work, the face of a bird was shown to be
produced by the working together of the morphogenetic protein Noggin
and a vitamin A derivative called retinoic acid (Lee, Fu, Hui and
Richman, 2001, pp. 909-912). Retinoic acid is a nuclear receptor.
Surely each creature is "fearfully and wonderfully made."
Acknowledgements
I thank Paul Stanton for computer typing, George Howe for constructive
criticism, and Sharron Hotchkiss for manuscript preparation.
References
CRSQ; Creation Re.~earch Society Quarterly.
Ashe, H. L. and M. Levine. 1999. Local inhibition and long range
enhancement of dpp signal transduction by sog. Nature 398:427-431.
Brown, C. 1989. A mathematical illustration of the law of symmetric
variation. CRSQ 26:18-19.
_____. 1999. The principle symmetric variation as it relates to
silent mutations. CRSQ 36: 1 00.
_____. 2001. The production of form, Hox genes, and symmetric variation.
CRSQ 38:48-49.
Costa, A. and P. Schedi. 200 I. Conservation signals location. Nature
381:593-595.
De Celis, J. F., E Barrio, and F. C. Katatos. 1996. A gene complex
acting downstream of dpp in Drosophila wing morpho…
Creation Research
Quarterly Volume 40, March 2004
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