|Abstract. San Francisco Meeting of the Federation
of American Societies for Experimental Biology (1999) FASEB.J. 13, A1543.
HALDANE'S RULE EXISTS SINCE REPRODUCTIVE
AND SPECIES DIFFERENTIATIONS BOTH REQUIRE "REPRODUCTIVE ISOLATION".
The prevention of recombination by some form of reproductive isolation (Romanes 1886; J. Linn. Soc. 19, 337-411) is necessary to initiate and preserve both sexual phenotypic differences within species, and phenotypic differences between species.
The heterogametic sex has different sex chromosomes and for regions containing genes affecting sexual differentiation there must be the equivalent of the hybrid sterility observed when members of allied species cross. The heteromorphic chromosomes seen in the heterogametic sex probably evolved from homomorphic chromosomes, where reproductive isolation initiated.
The antirecombinational effect of (C+G)% divergence proposed for incipient speciation (Forsdyke 1996; J. Theor. Biol. 178, 405-417) is applicable, in principle, to incipient sexual differentiation. As with speciation, subsequent chromosomal macromutations (e.g. segment deletions) might have substituted for the (C+G)% divergence, so that no trace of the original mechanism of reproductive isolation would be evident in many modern species. However, a step towards speciation would have been taken in the heterogametic sex.
A corollary of this is that incipient speciation, manifest as some degree of hybrid sterility when "varieties" are crossed, should appear at the earliest stage in the heterogametic sex, even in genera with homomorphic sex chromosomes (Haldane's rule for hybrid sterility). Later the differentiation would extend to autosomes, and reproductive isolation between the "varieties" (then by definition "species") would be complete. A proposed mechanism for Haldane's rule for hybrid inviability depends on differences in dosage compensation (Forsdyke 1995; J. Theor. Biol. 172. 335-345), and should not apply to species with homomorphic sex chromosomes (Presgraves & Orr 1998; Science 282, 952-954). For more (Click Here).
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Last edited 24 Mar 2000 by Donald Forsdyke