A novel highly divergent protein family identified from a viviparous insect by RNA-seq analysis: a potential target for tsetse fly-specific abortifacients.

In tsetse flies, nutrients for intrauterine larval development are synthesized by the modified accessory gland (milk gland) and provided in mother's milk during lactation. Interference with at least two milk proteins has been shown to extend larval development and reduce fecundity. The goal of...

Full description

Bibliographic Details
Main Authors: Joshua B Benoit, Geoffrey M Attardo, Veronika Michalkova, Tyler B Krause, Jana Bohova, Qirui Zhang, Aaron A Baumann, Paul O Mireji, Peter Takáč, David L Denlinger, Jose M Ribeiro, Serap Aksoy
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-04-01
Series:PLoS Genetics
Online Access:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1003874&type=printable
_version_ 1826587363392880640
author Joshua B Benoit
Geoffrey M Attardo
Veronika Michalkova
Tyler B Krause
Jana Bohova
Qirui Zhang
Aaron A Baumann
Paul O Mireji
Peter Takáč
David L Denlinger
Jose M Ribeiro
Serap Aksoy
author_facet Joshua B Benoit
Geoffrey M Attardo
Veronika Michalkova
Tyler B Krause
Jana Bohova
Qirui Zhang
Aaron A Baumann
Paul O Mireji
Peter Takáč
David L Denlinger
Jose M Ribeiro
Serap Aksoy
author_sort Joshua B Benoit
collection DOAJ
description In tsetse flies, nutrients for intrauterine larval development are synthesized by the modified accessory gland (milk gland) and provided in mother's milk during lactation. Interference with at least two milk proteins has been shown to extend larval development and reduce fecundity. The goal of this study was to perform a comprehensive characterization of tsetse milk proteins using lactation-specific transcriptome/milk proteome analyses and to define functional role(s) for the milk proteins during lactation. Differential analysis of RNA-seq data from lactating and dry (non-lactating) females revealed enrichment of transcripts coding for protein synthesis machinery, lipid metabolism and secretory proteins during lactation. Among the genes induced during lactation were those encoding the previously identified milk proteins (milk gland proteins 1-3, transferrin and acid sphingomyelinase 1) and seven new genes (mgp4-10). The genes encoding mgp2-10 are organized on a 40 kb syntenic block in the tsetse genome, have similar exon-intron arrangements, and share regions of amino acid sequence similarity. Expression of mgp2-10 is female-specific and high during milk secretion. While knockdown of a single mgp failed to reduce fecundity, simultaneous knockdown of multiple variants reduced milk protein levels and lowered fecundity. The genomic localization, gene structure similarities, and functional redundancy of MGP2-10 suggest that they constitute a novel highly divergent protein family. Our data indicates that MGP2-10 function both as the primary amino acid resource for the developing larva and in the maintenance of milk homeostasis, similar to the function of the mammalian casein family of milk proteins. This study underscores the dynamic nature of the lactation cycle and identifies a novel family of lactation-specific proteins, unique to Glossina sp., that are essential to larval development. The specificity of MGP2-10 to tsetse and their critical role during lactation suggests that these proteins may be an excellent target for tsetse-specific population control approaches.
first_indexed 2024-12-13T23:44:51Z
format Article
id doaj.art-80894154e2344fe380b335c677536e78
institution Directory Open Access Journal
issn 1553-7390
1553-7404
language English
last_indexed 2025-03-14T16:24:15Z
publishDate 2014-04-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Genetics
spelling doaj.art-80894154e2344fe380b335c677536e782025-02-22T05:31:58ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042014-04-01104e100387410.1371/journal.pgen.1003874A novel highly divergent protein family identified from a viviparous insect by RNA-seq analysis: a potential target for tsetse fly-specific abortifacients.Joshua B BenoitGeoffrey M AttardoVeronika MichalkovaTyler B KrauseJana BohovaQirui ZhangAaron A BaumannPaul O MirejiPeter TakáčDavid L DenlingerJose M RibeiroSerap AksoyIn tsetse flies, nutrients for intrauterine larval development are synthesized by the modified accessory gland (milk gland) and provided in mother's milk during lactation. Interference with at least two milk proteins has been shown to extend larval development and reduce fecundity. The goal of this study was to perform a comprehensive characterization of tsetse milk proteins using lactation-specific transcriptome/milk proteome analyses and to define functional role(s) for the milk proteins during lactation. Differential analysis of RNA-seq data from lactating and dry (non-lactating) females revealed enrichment of transcripts coding for protein synthesis machinery, lipid metabolism and secretory proteins during lactation. Among the genes induced during lactation were those encoding the previously identified milk proteins (milk gland proteins 1-3, transferrin and acid sphingomyelinase 1) and seven new genes (mgp4-10). The genes encoding mgp2-10 are organized on a 40 kb syntenic block in the tsetse genome, have similar exon-intron arrangements, and share regions of amino acid sequence similarity. Expression of mgp2-10 is female-specific and high during milk secretion. While knockdown of a single mgp failed to reduce fecundity, simultaneous knockdown of multiple variants reduced milk protein levels and lowered fecundity. The genomic localization, gene structure similarities, and functional redundancy of MGP2-10 suggest that they constitute a novel highly divergent protein family. Our data indicates that MGP2-10 function both as the primary amino acid resource for the developing larva and in the maintenance of milk homeostasis, similar to the function of the mammalian casein family of milk proteins. This study underscores the dynamic nature of the lactation cycle and identifies a novel family of lactation-specific proteins, unique to Glossina sp., that are essential to larval development. The specificity of MGP2-10 to tsetse and their critical role during lactation suggests that these proteins may be an excellent target for tsetse-specific population control approaches.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1003874&type=printable
spellingShingle Joshua B Benoit
Geoffrey M Attardo
Veronika Michalkova
Tyler B Krause
Jana Bohova
Qirui Zhang
Aaron A Baumann
Paul O Mireji
Peter Takáč
David L Denlinger
Jose M Ribeiro
Serap Aksoy
A novel highly divergent protein family identified from a viviparous insect by RNA-seq analysis: a potential target for tsetse fly-specific abortifacients.
PLoS Genetics
title A novel highly divergent protein family identified from a viviparous insect by RNA-seq analysis: a potential target for tsetse fly-specific abortifacients.
title_full A novel highly divergent protein family identified from a viviparous insect by RNA-seq analysis: a potential target for tsetse fly-specific abortifacients.
title_fullStr A novel highly divergent protein family identified from a viviparous insect by RNA-seq analysis: a potential target for tsetse fly-specific abortifacients.
title_full_unstemmed A novel highly divergent protein family identified from a viviparous insect by RNA-seq analysis: a potential target for tsetse fly-specific abortifacients.
title_short A novel highly divergent protein family identified from a viviparous insect by RNA-seq analysis: a potential target for tsetse fly-specific abortifacients.
title_sort novel highly divergent protein family identified from a viviparous insect by rna seq analysis a potential target for tsetse fly specific abortifacients
url https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1003874&type=printable
work_keys_str_mv AT joshuabbenoit anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT geoffreymattardo anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT veronikamichalkova anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT tylerbkrause anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT janabohova anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT qiruizhang anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT aaronabaumann anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT paulomireji anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT petertakac anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT davidldenlinger anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT josemribeiro anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT serapaksoy anovelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT joshuabbenoit novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT geoffreymattardo novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT veronikamichalkova novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT tylerbkrause novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT janabohova novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT qiruizhang novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT aaronabaumann novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT paulomireji novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT petertakac novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT davidldenlinger novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT josemribeiro novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients
AT serapaksoy novelhighlydivergentproteinfamilyidentifiedfromaviviparousinsectbyrnaseqanalysisapotentialtargetfortsetseflyspecificabortifacients