
Luciano Matzkin
· Associate Professor, EntomologyVerifiedUniversity of Arizona · Entomology
Active 2001–2026
About
Luciano M. Matzkin is a professor at the University of Arizona, holding appointments in the Department of Entomology, the Department of Ecology and Evolutionary Biology, and the BIO5 Institute. He has been a faculty member at the University of Arizona since 2017, initially as an Associate Professor and then as a Professor from 2024 onward. Dr. Matzkin earned his PhD in 2003 from Stony Brook University in the Department of Ecology and Evolutionary Biology and completed his undergraduate studies with a BS in 1996 at the University of California Irvine in the same field. His professional contact information includes an office in the Marley Building 641F and a phone number at the University of Arizona. The information provided does not include specific details about his research focus or key contributions.
Research topics
- Biology
- Genetics
- Computer Science
- Ecology
- Computational biology
- Neuroscience
- Demography
- Zoology
- Evolutionary biology
Selected publications
Figshare · 2026-04-02
articleOpen accessSupplementary Material 1.
Figshare · 2026-04-02
otherOpen accessAbstract Host plant range of insect herbivores may evolve towards generalization and specialization. However, how generalist herbivores achieve polyphagy and what facilitate host-plant range oscillation remains elusive. Our recent finding of a negative correlation between host-plant range and genome size in the Helicoverpa lineage predicts that the generalist Helicoverpa armigera, rather than its ancestral specialist sibling Helicoverpa assulta, should have a larger secretome size to modify host defenses, nutrients and/or structure, and should purge a significant amount of transposable elements (TEs) to minimize pseudogenization of genes associated with host utilization. To test these two predictions, we compared the sizes and compositions of the larval labial salivary gland transcriptomes of these two species, as well as the numbers of pseudogenes in four host defense detoxification gene families in their genomes. Indeed, the labial salivary gland transcriptome of H. armigera was significantly greater than that of H. assulta at both the contig and gene levels, especially for the Gene Ontology (GO) terms and KEGG pathways associated the main functions of the larval salivary gland, such as protein synthesis and secretion, herbivore offence, digestion, detoxification. By contrast, H. assulta had more contigs inserted with TEs, more transcripts involved in transposition of TEs, and more pseudogenized host defense detoxification genes. These results not only match the predictions but also demonstrate that oscillation of host plant range evolution in Helicoverpa species is at least in part facilitated by TE-mediate pseudogenization (shutdown) and reactivation (on) of host use and secretion-related genes.
BMC Biology · 2026-04-16
articleOpen accessBACKGROUND: Reproductive proteins evolve rapidly, making them strong candidates for driving postmating-prezygotic (PMPZ) reproductive mismatches between populations. While most previous studies have focused on protein sequence divergence as a likely driver of PMPZ disruptions, reproductive proteomes may also diverge compositionally and/or quantitatively. RESULTS: Here, we combine quantitative proteomics, molecular evolutionary analyses, and protein-protein interaction (PPI) modeling to predict the molecular basis of reproductive mismatches between Drosophila mojavensis and D. arizonae. We demonstrate multidimensional divergence in reproductive proteomes including changes at the sequence, compositional, and quantitative levels. We further demonstrate that three divergent male seminal fluid proteins affect the size of the insemination reaction mass and/or fertilization success in D. arizonae. Despite high sequence divergence, predicted protein-protein interactions involving a conserved set of proteases and/or protease inhibitors were predicted to be maintained in heterospecific crosses. In contrast, predicted interspecies protein mismatches arose from proteome compositional divergence, suggesting that such changes may play a disproportionate role in PMPZ isolation, at least for the subset of the interactome that we tested. Furthermore, extensive quantitative divergence, particularly for proteases and inhibitors, suggests pervasive stoichiometric mismatches in heterospecific matings. CONCLUSIONS: Altogether, our findings indicate that reproductive proteins are evolutionarily labile at multiple levels, and that compositional and quantitative divergence, rather than sequence changes alone, may be central to the early evolution of reproductive isolation.
BMC Genomics · 2026-04-02
articleOpen accessHost plant range of insect herbivores may evolve towards generalization and specialization. However, how generalist herbivores achieve polyphagy and what facilitate host-plant range oscillation remains elusive. Our recent finding of a negative correlation between host-plant range and genome size in the Helicoverpa lineage predicts that the generalist Helicoverpa armigera, rather than its ancestral specialist sibling Helicoverpa assulta, should have a larger secretome size to modify host defenses, nutrients and/or structure, and should purge a significant amount of transposable elements (TEs) to minimize pseudogenization of genes associated with host utilization. To test these two predictions, we compared the sizes and compositions of the larval labial salivary gland transcriptomes of these two species, as well as the numbers of pseudogenes in four host defense detoxification gene families in their genomes. Indeed, the labial salivary gland transcriptome of H. armigera was significantly greater than that of H. assulta at both the contig and gene levels, especially for the Gene Ontology (GO) terms and KEGG pathways associated the main functions of the larval salivary gland, such as protein synthesis and secretion, herbivore offence, digestion, detoxification. By contrast, H. assulta had more contigs inserted with TEs, more transcripts involved in transposition of TEs, and more pseudogenized host defense detoxification genes. These results not only match the predictions but also demonstrate that oscillation of host plant range evolution in Helicoverpa species is at least in part facilitated by TE-mediate pseudogenization (shutdown) and reactivation (on) of host use and secretion-related genes.
Open MIND · 2026-01-01
otherOpen access1st authorCorrespondingBackground: Reproductive proteins evolve rapidly, making them strong candidates for driving postmating-prezygotic (PMPZ) reproductive mismatches between populations. While most previous studies have focused on protein sequence divergence as a likely driver of PMPZ disruptions, reproductive proteomes may also diverge compositionally and/or quantitatively. Results: Here, we combine quantitative proteomics, molecular evolutionary analyses, and protein-protein interaction (PPI) modeling to predict the molecular basis of reproductive mismatches between Drosophila mojavensis and D. arizonae. We demonstrate multidimensional divergence in reproductive proteomes including changes at the sequence, compositional, and quantitative levels. We further demonstrate that three divergent male seminal fluid proteins affect the size of the insemination reaction mass and/or fertilization success in D. arizonae. Despite high sequence divergence, predicted protein-protein interactions involving a conserved set of proteases and/or protease inhibitors were predicted to be maintained in heterospecific crosses. In contrast, predicted interspecies protein mismatches arose from proteome compositional divergence, suggesting that such changes may play a disproportionate role in PMPZ isolation, at least for the subset of the interactome that we tested. Furthermore, extensive quantitative divergence, particularly for proteases and inhibitors, suggests pervasive stoichiometric mismatches in heterospecific matings. Conclusions: Altogether, our findings indicate that reproductive proteins are evolutionarily labile at multiple levels, and that compositional and quantitative divergence, rather than sequence changes alone, may be central to the early evolution of reproductive isolation.
Figshare · 2026-04-02
datasetOpen accessSupplementary Material 2.
OSF Preprints (OSF Preprints) · 2026-04-02
otherSenior authorBackground: Reproductive proteins evolve rapidly, making them strong candidates for driving postmating-prezygotic (PMPZ) reproductive mismatches between populations. While most previous studies have focused on protein sequence divergence as a likely driver of PMPZ disruptions, reproductive proteomes may also diverge compositionally and/or quantitatively. Results: Here, we combine quantitative proteomics, molecular evolutionary analyses, and protein-protein interaction (PPI) modeling to predict the molecular basis of reproductive mismatches between Drosophila mojavensis and D. arizonae. We demonstrate multidimensional divergence in reproductive proteomes including changes at the sequence, compositional, and quantitative levels. We further demonstrate that three divergent male seminal fluid proteins affect the size of the insemination reaction mass and/or fertilization success in D. arizonae. Despite high sequence divergence, predicted protein-protein interactions involving a conserved set of proteases and/or protease inhibitors were predicted to be maintained in heterospecific crosses. In contrast, predicted interspecies protein mismatches arose from proteome compositional divergence, suggesting that such changes may play a disproportionate role in PMPZ isolation, at least for the subset of the interactome that we tested. Furthermore, extensive quantitative divergence, particularly for proteases and inhibitors, suggests pervasive stoichiometric mismatches in heterospecific matings. Conclusions: Altogether, our findings indicate that reproductive proteins are evolutionarily labile at multiple levels, and that compositional and quantitative divergence, rather than sequence changes alone, may be central to the early evolution of reproductive isolation.
Figshare · 2026-04-02
datasetOpen accessSupplementary Material 2.
Figshare · 2026-04-02
articleOpen accessSupplementary Material 1.
Figshare · 2026-04-02
otherOpen accessAbstract Host plant range of insect herbivores may evolve towards generalization and specialization. However, how generalist herbivores achieve polyphagy and what facilitate host-plant range oscillation remains elusive. Our recent finding of a negative correlation between host-plant range and genome size in the Helicoverpa lineage predicts that the generalist Helicoverpa armigera, rather than its ancestral specialist sibling Helicoverpa assulta, should have a larger secretome size to modify host defenses, nutrients and/or structure, and should purge a significant amount of transposable elements (TEs) to minimize pseudogenization of genes associated with host utilization. To test these two predictions, we compared the sizes and compositions of the larval labial salivary gland transcriptomes of these two species, as well as the numbers of pseudogenes in four host defense detoxification gene families in their genomes. Indeed, the labial salivary gland transcriptome of H. armigera was significantly greater than that of H. assulta at both the contig and gene levels, especially for the Gene Ontology (GO) terms and KEGG pathways associated the main functions of the larval salivary gland, such as protein synthesis and secretion, herbivore offence, digestion, detoxification. By contrast, H. assulta had more contigs inserted with TEs, more transcripts involved in transposition of TEs, and more pseudogenized host defense detoxification genes. These results not only match the predictions but also demonstrate that oscillation of host plant range evolution in Helicoverpa species is at least in part facilitated by TE-mediate pseudogenization (shutdown) and reactivation (on) of host use and secretion-related genes.
Recent grants
RIG: Genetic mechanisms of detoxification in the cactophilic Drosophila mojavensis
NSF · $128k · 2011–2014
Frequent coauthors
- 30 shared
Carson W. Allan
University of Arizona
- 23 shared
Therese A. Markow
University of California, San Diego
- 16 shared
Coline C. Jaworski
Institut Sophia Agrobiotech
- 15 shared
Jeremy M. Bono
University of Colorado Colorado Springs
- 14 shared
Fernando Dı́az
Ensenada Institute of Technology
- 11 shared
Kyle M. Benowitz
Arizona State University
- 10 shared
Walter F. Eanes
Stony Brook University
- 8 shared
Joshua M. Coleman
University of Arizona
Labs
Education
- 2003
PhD, Ecology and Evolution
Stony Brook University
- 1996
BS, Ecology and Evolutionary Biology
University of California Irvine
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