Transcriptional Regulation of Reproductive Diapause in the Convergent Lady Beetle, <i>Hippodamia convergens</i>

Diapause is an alternate development program that synchronizes an insect’s life cycle with seasonally abundant resources and ensures survival in unfavorable conditions. The physiological basis of diapause has been well characterized, but the molecular mechanisms regulating it are still being elucida...

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Main Authors: Emily A. W. Nadeau, Melise C. Lecheta, John J. Obrycki, Nicholas M. Teets
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Insects
Subjects:
Online Access:https://www.mdpi.com/2075-4450/13/4/343
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author Emily A. W. Nadeau
Melise C. Lecheta
John J. Obrycki
Nicholas M. Teets
author_facet Emily A. W. Nadeau
Melise C. Lecheta
John J. Obrycki
Nicholas M. Teets
author_sort Emily A. W. Nadeau
collection DOAJ
description Diapause is an alternate development program that synchronizes an insect’s life cycle with seasonally abundant resources and ensures survival in unfavorable conditions. The physiological basis of diapause has been well characterized, but the molecular mechanisms regulating it are still being elucidated. Here, we present a <i>de novo</i> transcriptome and quantify transcript expression during diapause in the convergent lady beetle <i>Hippodamia convergens</i>. <i>H. convergens</i> is used as an augmentative biocontrol agent, and adult females undergo reproductive diapause that is regulated by photoperiod. We sampled females at three stages (early, mid, and late diapause) and compared transcript expression to non-diapausing individuals. Based on principle component analysis, the transcriptomes of diapausing beetles were distinct from non-diapausing beetles, and the three diapausing points tended to cluster together. However, there were still classes of transcripts that differed in expression across distinct phases of diapause. In general, transcripts involved in muscle function and flight were upregulated during diapause, likely to support dispersal flights that occur during diapause, while transcripts involved in ovarian development were downregulated. This information could be used to improve biological control by manipulating diapause. Additionally, our data contribute to a growing understanding of the genetic regulation of diapause across diverse insects.
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spelling doaj.art-2763ac28726446d888d2f180fb55eb602023-12-03T13:32:07ZengMDPI AGInsects2075-44502022-03-0113434310.3390/insects13040343Transcriptional Regulation of Reproductive Diapause in the Convergent Lady Beetle, <i>Hippodamia convergens</i>Emily A. W. Nadeau0Melise C. Lecheta1John J. Obrycki2Nicholas M. Teets3Department of Entomology, College of Agriculture, Food and Environment, University of Kentucky, Lexington, KY 40546, USADepartment of Entomology, College of Agriculture, Food and Environment, University of Kentucky, Lexington, KY 40546, USADepartment of Entomology, College of Agriculture, Food and Environment, University of Kentucky, Lexington, KY 40546, USADepartment of Entomology, College of Agriculture, Food and Environment, University of Kentucky, Lexington, KY 40546, USADiapause is an alternate development program that synchronizes an insect’s life cycle with seasonally abundant resources and ensures survival in unfavorable conditions. The physiological basis of diapause has been well characterized, but the molecular mechanisms regulating it are still being elucidated. Here, we present a <i>de novo</i> transcriptome and quantify transcript expression during diapause in the convergent lady beetle <i>Hippodamia convergens</i>. <i>H. convergens</i> is used as an augmentative biocontrol agent, and adult females undergo reproductive diapause that is regulated by photoperiod. We sampled females at three stages (early, mid, and late diapause) and compared transcript expression to non-diapausing individuals. Based on principle component analysis, the transcriptomes of diapausing beetles were distinct from non-diapausing beetles, and the three diapausing points tended to cluster together. However, there were still classes of transcripts that differed in expression across distinct phases of diapause. In general, transcripts involved in muscle function and flight were upregulated during diapause, likely to support dispersal flights that occur during diapause, while transcripts involved in ovarian development were downregulated. This information could be used to improve biological control by manipulating diapause. Additionally, our data contribute to a growing understanding of the genetic regulation of diapause across diverse insects.https://www.mdpi.com/2075-4450/13/4/343reproductive diapauseColeopterabiological controltranscriptomicsRNA-Seq
spellingShingle Emily A. W. Nadeau
Melise C. Lecheta
John J. Obrycki
Nicholas M. Teets
Transcriptional Regulation of Reproductive Diapause in the Convergent Lady Beetle, <i>Hippodamia convergens</i>
Insects
reproductive diapause
Coleoptera
biological control
transcriptomics
RNA-Seq
title Transcriptional Regulation of Reproductive Diapause in the Convergent Lady Beetle, <i>Hippodamia convergens</i>
title_full Transcriptional Regulation of Reproductive Diapause in the Convergent Lady Beetle, <i>Hippodamia convergens</i>
title_fullStr Transcriptional Regulation of Reproductive Diapause in the Convergent Lady Beetle, <i>Hippodamia convergens</i>
title_full_unstemmed Transcriptional Regulation of Reproductive Diapause in the Convergent Lady Beetle, <i>Hippodamia convergens</i>
title_short Transcriptional Regulation of Reproductive Diapause in the Convergent Lady Beetle, <i>Hippodamia convergens</i>
title_sort transcriptional regulation of reproductive diapause in the convergent lady beetle i hippodamia convergens i
topic reproductive diapause
Coleoptera
biological control
transcriptomics
RNA-Seq
url https://www.mdpi.com/2075-4450/13/4/343
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