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To: Alex Murphy
None of which addresses the core issue of the press release - were the test results exaggerated or not? Why does it matter who the whistle-blower is, if the allegations have any merit?

Good question. I'll have to see when the new jounal is published online (theoretically today), since my institution has an online sub. Usually, they have a valid point if it makes it into a journal like nature, though.

14 posted on 02/06/2002 10:15:07 AM PST by ThinkPlease
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To: ThinkPlease
Found it.

Don't know if you can read this(subscription necessary?) Abstract (or at least the first paragraph):

A fascinating question in biology is how molecular changes in developmental pathways lead to macroevolutionary changes in morphology. Mutations in homeotic (Hox) genes have long been suggested as potential causes of morphological evolution(1,2), and there is abundant evidence that some changes in Hox expression patterns correlate with transitions in animal axial pattern(3) . A major morphological transition in metazoans occurred about 400 million years ago, when six-legged insects diverged from crustacean-like arthropod ancestors with multiple limbs(4-7_. In Drosophila melanogaster and other insects, the Ultrabithorax (Ubx) and abdominal A (AbdA, also abd-A) Hox proteins are expressed largely in the abdominal segments, where they can suppress thoracic leg development during embryogenesis(3) . In a branchiopod crustacean, Ubx/AbdA proteins are expressed in both thorax and abdomen, including the limb primordia, but do not repress limbs(8-11) . Previous studies led us to propose that gain and loss of transcriptional activation and repression functions in Hox proteins was a plausible mechanism to diversify morphology during animal evolution(12) . Here we show that naturally selected alteration of the Ubx protein is linked to the evolutionary transition to hexapod limb pattern.

1. Goldschmidt, R. The Material Basis of Evolution (Yale Univ. Press, New Haven, Connecticut, 1940)

2. Lewis, E. B. A gene complex controlling segmentation in Drosophila. Nature 276, 565-570 (1978)

3. Carroll, S. B., Grenier, J. K. & Weatherbee, S. D. From DNA to Diversity (Blackwell Science, London, 2001)

4. Boore, J. L., Collins, T. M., Stanton, D., Daehler, L. L. & Brown, W. M. Deducing the pattern of arthropod phylogeny from mitochondrial DNA rearrangements. Nature 376, 163-165 (1995)

5. Friedrich, M. & Tautz, D. Ribosomal DNA phylogeny of the major extant arthropod classes and the evolution of myriapods. Nature 376, 165-167 (1995)

6. Aguinaldo, A. et al. Evidence for a clade of nematodes, arthropods and other moulting animals. Nature 387, 489-493 (1997)

7. Regier, J. C. & Shultz, J. W. Molecular phylogeny of the major arthropod groups indicates polyphyly of crustaceans and a new hypothesis for the origin of hexapods. Mol. Biol. Evol. 14, 902-913 (1997)

8. Averof, M. & Akam, M. Hox genes and the diversification of insect and crustacean body plans. Nature 376, 420-423 (1995)

9. Averof, M. & Patel, N. Crustacean appendage evolution associated with changes in Hox gene expression. Nature 388, 682-686 (1997) | Article

10. Panganiban, G., Sebring, A., Nagy, L. & Carroll, S. The development of crustacean limbs and the evolution of arthropods. Science 270, 1363-1366 (1995)

11. Abzhanov, A. & Kaufman, T. C. Crustacean (malacostracan) Hox genes and the evolution of the arthropod trunk. Development 127, 2239-2249 (2000)

12. Li, X. & McGinnis, W. Activity regulation of Hox proteins, a mechanism for altering functional specificity in development and evolution. Proc. Natl Acad. Sci. USA 96, 6802-6807 (1999)

13. Gonzalez-Reyes, A. & Morata, G. The developmental effect of overexpressing a Ubx product in Drosophila embryos is dependent on its interactions with other homeotic products. Cell 61, 515-522 (1990) | PubMed |

15 posted on 02/06/2002 10:26:51 AM PST by ThinkPlease
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