Drosophila subobscura Short Sperm have no Biochemical Incompatibilities with Fertilization
نویسنده
چکیده
Drosophila obscura group species produce two distinct sizes of nucleated sperm that differ only in head and tail lenghts. Between both sperm there is no differences in location of the acrosome and flagellum during spermiogenesis where each sperm type develops in its own bundle. Fertile sperm accumulate in the seminal vesicles. Fertilization is exclusively monospermic and in a previous study we suggested that both types of sperm are fertilization-competent on the basis of similar DNA content and storage in females also if morph variations are consistent with a fertilization-related selection for optimal sperm size. This assumption is in agreement with previous studies that demonstrated that only long sperm fertilize eggs. In this study fertilization of Drosophila subobscura is examined using anti-sperm surface -Nacetylhexosaminidases and -L-fucosidase antibodies. Beta hexosaminidases are intrinsic proteins of the sperm plasma membrane in spermomomorphic species of the melanogaster group closely related to Drosophila melanogaster. These enzymes had been previously identified as putative receptors for glycoconjugates of the egg surface, structurally and functionally conserved. Here their localization has been investigated in Drosophila subobscura. Consistent with our previous study, short and long sperm are functionally equivalent. More data are needed to clarify the consequences and adaptative significance of morph variations.
منابع مشابه
Rapid evolution of asymmetric reproductive incompatibilities in stalk-eyed flies.
The steps by which isolated populations acquire reproductive incompatibilities remain poorly understood. One potentially important process is postcopulatory sexual selection because it can generate divergence between populations in traits that influence fertilization success after copulation. Here we present a comprehensive analysis of this form of reproductive isolation by conducting reciproca...
متن کاملGametic incompatibilities between races of Drosophila melanogaster.
Reproductive-isolating mechanisms between nascent species may involve sperm-egg recognition and have been best described in externally fertilizing organisms where such recognition is essential in preventing undesirable fertilizations. However, reproductive barriers in internally fertilizing species differ in significant ways, and a direct role for sperm-egg interactions has yet to be demonstrat...
متن کاملSperm fate and function in reproductive isolation in Drosophila.
Central to the study of speciation is the identification of the isolating mechanisms that reduce gene flow. Of special interest are those isolating mechanisms that are the earliest to arise. Sperm fate and function play a major role in two distinct types of reproductive isolation in the genus Drosophila. First, postcopulatory-prezygotic (PCPZ) incompatibilities between the male ejaculate and a ...
متن کاملPerception of male-male competition influences Drosophila copulation behaviour even in species where females rarely remate.
Males in many taxa are known to exhibit behavioural plasticity in response to the perceived intensity of sperm competition, reflected in Drosophila melanogaster by increased copulation duration following prior exposure to a rival. We tested the prediction that males do not adjust their copulation effort in response to the presence of a competitor in Drosophila species where there is little or n...
متن کاملIntegrated and independent evolution of heteromorphic sperm types
Sperm are a simple cell type with few components, yet they exhibit tremendous between-species morphological variation in those components thought to reflect selection in different fertilization environments. However, within a species, sperm components are expected to be selected to be functionally integrated for optimal fertilization of eggs. Here, we take advantage of within-species variation ...
متن کامل