The utility of transcriptomics in the conservation of
sensitive and economically important species
Bharat
Bhusan Patnaik1,2,3*ϯand Yong Seok Lee2,3
ϯConsulting Editor,
Journal of Environmental Biology, Lucknow-226 022, India
1P.G Department of
Biosciences and Biotechnology, Fakir Mohan University, Balasore-756 089,
India
2Department of
Biology, College of Natural Sciences, Soonchunhyang University,
Chungnam-31538, South Korea
3Korea Native
Animal Resources Utilization Convergence Research Institute (KNAR),
Soonchunhyang University, Chungnam-31538, South Korea
*Corresponding
Author Email : drbharatbhusan4@gmail.com
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Abstract
The connection
between the central dogma of biology [DNA --(Transcription)---› RNA
–(Translation)--› Protein] and the 'omics' resources obtained from each
molecule are now being exploited by conservation managers to protect
biodiversity and ecosystems for sustainable development. Biodiversity doesn't
necessarily mean the total number of species, it is more complex and includes
genetic diversity within species and the diversity of habitats. Land-use
changes, direct harvest, various forms of pollution, and climate change are
the biggest threats to biodiversity, most of which are hardly documented at
the molecular level to guide conservation actions and stop extinctions.
Justifying the plasticity of species adaptability could ensure informed
decisions on proposing suitable habitats for species translocations if the
current distributional range is disturbed. The 'omics' resources (especially
generated by high-throughput RNA and DNA sequencing approaches) have
intervened on a larger scale recently to understand species physiology,
evolutionary biology and ecology. This has supported enriched information on
the evolution and evaluation of adaptive phenotypes in natural populations as
well as the mechanism of physiological responses to various environmental
perturbations (Alvarez et al., 2015; De Wit et al., 2015;
Evans, 2015; Connon et al., 2018).
Transcriptomics
can unravel unparalleled mysteries in the context of conservation of
sensitive and economically important species. Being smaller than genomes and
tissue-specific, it reduces the amount of data generated and focuses on
candidate gene expressions, understanding a species' response to
environmental changes. It gives sufficient scope for studying the biology of
a non-model species at the molecular level by de novo assembled transcript
generation and annotation involving predicted gene function. Apart from the
ontology and homology-based functional annotations, the transcriptomes can
also be mined for the discovery of genetic markers such as simple sequence
repeats (SSRs) and single nucleotide polymorphisms (SNPs) vital for
assessments of genetic diversity and exploring species from newer habitats.
Ultimately, such resources should be effectively integrated into management
decisions and policies to contribute towards conservation. Utilization of
transcriptome knowledge in conservation remains rare due to unfamiliarity of
the interpretation of complex molecular data for managers. Hence, to overcome
such a knowledge divide, the physiologists and the data scientists need to
build partnerships with regulatory agencies and resource managers to
translate transcriptomic evaluations to well-characterized molecular thresholds
that can act as sensible markers to predict a species' adaptive plasticity in
invoking compensatory mechanisms leading to recovery or non-recovery. Until
and unless such conservative benchmarks are designed, the utility of the
transcriptomes into management actions and policies seems debated.
I
have been associated with the Korean threatened species initiative for the
past eight years as a researcher. The initiative has prioritized the Illumina
HiSeq-based short-read platform for transcriptome generation and the Trinity
suite for de novo assembly of clean reads. Further, a locally-curated
database known as the PANM database (Protostome DB) has facilitated gene
discovery in Red List molluscan and butterfly species of Korea that are
threatened of extinction. Mostly, the transcriptomics pipeline adopted under
this initiative has cataloged the functional resources in the context of
immunity, growth and reproduction of species. Large-scale screening of SSR
markers from transcriptome has highlighted the possibility of addressing
species richness and diversity in disturbed natural habitats and the
feasibility of finding species in newer habitats. This initiative has
provided the first report to record ecologically-relevant traits from
endangered lycaenid butterflies such as Protantigius superans and Spindasis
takanosis and the nymphalid butterfly, Fabriciana nerippe (Patnaik
et al., 2015; Hwang et al., 2016). Further, the transcriptome
profile of the Asian giant hornet, Vespa mandarinia was able to screen
new genes to understand the physiological attributes of the wasp enlisted as
threatened species in Korea (Patnaik et al., 2016). Among the
threatened molluscan species of Korea, the land snails such as Aegista
chejuensis and Aegista quelpartensis (Kang et al., 2016), Koreanohadra
kurodana (Kang et al., 2016), Satsuma myomphala (Kang et
al., 2017) and Ellobium chinense (Kang et al., 2018) were
prioritized for transcriptome sequencing. The detailed molecular components
ascribed to innate immunity pathways were also screened from the
transcriptome of a freshwater mussel, Cristaria plicata endangered in
Korea (Patnaik et al., 2016) and an air-breathing land slug, Incilaria
fruhstorferi (Patnaik et al., 2019). The discovery of the immunity
components was useful in drafting a conceptual map of innate immune signaling
in molluscs by addressing the putative involvement of the orthologs at
different stages of pathway. Such resources are vital for functional genomics
applications as they serve to understand the resistance or susceptibility of
the host to microorganisms. De novo transcriptome of endangered triton
shell, Charonia lampas sauliae identified transcripts that are channel
proteins blocked by tetrodotoxin synthesized by symbiotic bacteria inhabiting
the shells. Additionally, conotoxin superfamily peptides were discovered that
could be synthesized for therapeutic interventions such as anti-cancer and
pain-relief agents (Fassio et al., 2019; Yao et al., 2019;
Hwang et al., 2021).The transcriptome of endangered diving beetle, Cybister
japonicus and endangered dung beetle Copris tripartitus also enriched
information on molecular resources including SSR discovery (Hwang et al.,
2018; Hwang et al., 2023). With the large-scale availability of
'omics' resources, the threatened species initiative is taking proactive
steps to complement local conservation efforts in the country.
In
India, there is a lack of similar consortium-based initiatives for
understanding the local biodiversity of a region. This has restricted access
to high-throughput molecular resources from the local biodiversity for
meeting the challenges in health, agrifood and the environment. Hence, a
consortium such as the National Biodiversity Genomics (NBG) consortium
addressing the genome or transcriptome-guided discovery of molecular
resources can act as a knowledge hub supporting environmental sustainability
(Fig. 1). The consortium will be able to develop expertise in database
development, bigdata analysis and bioinformatics, genetic diversity analysis
and functional genomics resources. The consortium will also facilitate new
opportunities in bigdata science, research-academia-industry partnerships for
new product development, entrepreneurship, and outreach activities and invoke
a forum for collaborations with International genomics consortiums. Such a
consortium will keep the academics interested in the research supporting
environmental sustainability with opportunities for workshops/ training,
open-learning and modular courses, environmental education programs to
encourage local action groups and conservation managers and create avenues
for convergence research for resource utilization. Building 'omics' data
infrastructure in a consortium to study the conservation of sensitive and
economically-important species is needed in the country to invigorate
attention on biodiversity conservation. In summary, such a consortium will
build large-scale data resources, maximize the impact of national research
infrastructure, build scientific capabilities, catalyze scientific
collaborations and international linkages, and would accelerate research and
translation into industry.
I
sincerely wish that the reference transcriptome characterization of native
flora and fauna would be taken up in a consortium mode to unravel the
unparalleled benefits of the resources in multi-dimensional research and
development objectives. I am happy to share my research experience and
expertise through this editorial on the 'Journal of Environmental Biology
(JEB)' platform- a journal that I have been associated with for the last 15
years in different capacities as an author, reviewer, and editor. I appreciate
the visions of Professor Dalela and the hardworking team over the years to
make this journal a global environmental outlook tool for the benefit of
society.
Acknowledgment: This research was
supported by Korea Basic Science Institute (National research Facilities and
Equipment Center) grant funded by the Ministry of Education
(2022R1A6C101B794), the National Research Foundation (NRF-2021R1A6A1A03039503
/ NRF-2017R1D1A3B06034971) and Soonchunhyang University Research
Fund.Further, the authors solicit the support received from the Agreement of
Cooperation between Fakir Mohan University, Balasore, India and KNAR,
Soonchunhyang University, Asan, Korea.
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