Identification, RNAi knockdown, and functional analysis of an ejaculate protein that mediates a postmating, prezygotic phenotype in a cricket.
Postmating, prezygotic phenotypes, especially those that underlie reproductive isolation between closely related species, have been a central focus of evolutionary biologists over the past two decades. Such phenotypes are thought to evolve rapidly and be nearly ubiquitous among sexually reproducing...
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2009-10-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC2761614?pdf=render |
id |
doaj-618abdf3a5b74ba8a3b415862ec1c5c9 |
---|---|
record_format |
Article |
spelling |
doaj-618abdf3a5b74ba8a3b415862ec1c5c92020-11-25T00:26:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-10-01410e753710.1371/journal.pone.0007537Identification, RNAi knockdown, and functional analysis of an ejaculate protein that mediates a postmating, prezygotic phenotype in a cricket.Jeremy L MarshallDiana L HuestisYasuaki HiromasaShanda WheelerCris OppertSusan A MarshallJohn M TomichBrenda OppertPostmating, prezygotic phenotypes, especially those that underlie reproductive isolation between closely related species, have been a central focus of evolutionary biologists over the past two decades. Such phenotypes are thought to evolve rapidly and be nearly ubiquitous among sexually reproducing eukaryotes where females mate with multiple partners. Because these phenotypes represent interplay between the male ejaculate and female reproductive tract, they are fertile ground for reproductive senescence--as ejaculate composition and female physiology typically change over an individual's life span. Although these phenotypes and their resulting dynamics are important, we have little understanding of the proteins that mediate these phenotypes, particularly for species groups where postmating, prezygotic traits are the primary mechanism of reproductive isolation. Here, we utilize proteomics, RNAi, mating experiments, and the Allonemobius socius complex of crickets, whose members are primarily isolated from one another by postmating, prezygotic phenotypes (including the ability of a male to induce a female to lay eggs), to demonstrate that one of the most abundant ejaculate proteins (a male accessory gland-biased protein similar to a trypsin-like serine protease) decreases in abundance over a male's reproductive lifetime and mediates the induction of egg-laying in females. These findings represent one of the first studies to identify a protein that plays a role in mediating both a postmating, prezygotic isolation pathway and reproductive senescence.http://europepmc.org/articles/PMC2761614?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jeremy L Marshall Diana L Huestis Yasuaki Hiromasa Shanda Wheeler Cris Oppert Susan A Marshall John M Tomich Brenda Oppert |
spellingShingle |
Jeremy L Marshall Diana L Huestis Yasuaki Hiromasa Shanda Wheeler Cris Oppert Susan A Marshall John M Tomich Brenda Oppert Identification, RNAi knockdown, and functional analysis of an ejaculate protein that mediates a postmating, prezygotic phenotype in a cricket. PLoS ONE |
author_facet |
Jeremy L Marshall Diana L Huestis Yasuaki Hiromasa Shanda Wheeler Cris Oppert Susan A Marshall John M Tomich Brenda Oppert |
author_sort |
Jeremy L Marshall |
title |
Identification, RNAi knockdown, and functional analysis of an ejaculate protein that mediates a postmating, prezygotic phenotype in a cricket. |
title_short |
Identification, RNAi knockdown, and functional analysis of an ejaculate protein that mediates a postmating, prezygotic phenotype in a cricket. |
title_full |
Identification, RNAi knockdown, and functional analysis of an ejaculate protein that mediates a postmating, prezygotic phenotype in a cricket. |
title_fullStr |
Identification, RNAi knockdown, and functional analysis of an ejaculate protein that mediates a postmating, prezygotic phenotype in a cricket. |
title_full_unstemmed |
Identification, RNAi knockdown, and functional analysis of an ejaculate protein that mediates a postmating, prezygotic phenotype in a cricket. |
title_sort |
identification, rnai knockdown, and functional analysis of an ejaculate protein that mediates a postmating, prezygotic phenotype in a cricket. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2009-10-01 |
description |
Postmating, prezygotic phenotypes, especially those that underlie reproductive isolation between closely related species, have been a central focus of evolutionary biologists over the past two decades. Such phenotypes are thought to evolve rapidly and be nearly ubiquitous among sexually reproducing eukaryotes where females mate with multiple partners. Because these phenotypes represent interplay between the male ejaculate and female reproductive tract, they are fertile ground for reproductive senescence--as ejaculate composition and female physiology typically change over an individual's life span. Although these phenotypes and their resulting dynamics are important, we have little understanding of the proteins that mediate these phenotypes, particularly for species groups where postmating, prezygotic traits are the primary mechanism of reproductive isolation. Here, we utilize proteomics, RNAi, mating experiments, and the Allonemobius socius complex of crickets, whose members are primarily isolated from one another by postmating, prezygotic phenotypes (including the ability of a male to induce a female to lay eggs), to demonstrate that one of the most abundant ejaculate proteins (a male accessory gland-biased protein similar to a trypsin-like serine protease) decreases in abundance over a male's reproductive lifetime and mediates the induction of egg-laying in females. These findings represent one of the first studies to identify a protein that plays a role in mediating both a postmating, prezygotic isolation pathway and reproductive senescence. |
url |
http://europepmc.org/articles/PMC2761614?pdf=render |
work_keys_str_mv |
AT jeremylmarshall identificationrnaiknockdownandfunctionalanalysisofanejaculateproteinthatmediatesapostmatingprezygoticphenotypeinacricket AT dianalhuestis identificationrnaiknockdownandfunctionalanalysisofanejaculateproteinthatmediatesapostmatingprezygoticphenotypeinacricket AT yasuakihiromasa identificationrnaiknockdownandfunctionalanalysisofanejaculateproteinthatmediatesapostmatingprezygoticphenotypeinacricket AT shandawheeler identificationrnaiknockdownandfunctionalanalysisofanejaculateproteinthatmediatesapostmatingprezygoticphenotypeinacricket AT crisoppert identificationrnaiknockdownandfunctionalanalysisofanejaculateproteinthatmediatesapostmatingprezygoticphenotypeinacricket AT susanamarshall identificationrnaiknockdownandfunctionalanalysisofanejaculateproteinthatmediatesapostmatingprezygoticphenotypeinacricket AT johnmtomich identificationrnaiknockdownandfunctionalanalysisofanejaculateproteinthatmediatesapostmatingprezygoticphenotypeinacricket AT brendaoppert identificationrnaiknockdownandfunctionalanalysisofanejaculateproteinthatmediatesapostmatingprezygoticphenotypeinacricket |
_version_ |
1725342477797294080 |