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Genetic characterization and phylogenetic analysis of the Nigella sativa (black seed) plastome
In this study, the complete plastome sequence of Nigella sativa (black seed), was analyzed for the first time. The plastome spans approximately 154,120 bp, comprising four sections: the Large Single-Copy (LSC) (85,538 bp), the Small Single-Copy (SSC) (17,984 bp), and two Inverted Repeat (IR) regions...
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Published in: | Scientific reports 2024-06, Vol.14 (1), p.14509-16, Article 14509 |
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description | In this study, the complete plastome sequence of
Nigella sativa
(black seed), was analyzed for the first time. The plastome spans approximately 154,120 bp, comprising four sections: the Large Single-Copy (LSC) (85,538 bp), the Small Single-Copy (SSC) (17,984 bp), and two Inverted Repeat (IR) regions (25,299 bp). A comparative study of
N. sativa
’s plastome with ten other species from various genera in the Ranunculaceae family reveals substantial structural variations. The contraction of the inverted repeat region in
N. sativa
influences the boundaries of single-copy regions, resulting in a shorter plastome size than other species. When comparing the plastome of
N. sativa
with those of its related species, significant divergence is observed, particularly except for
N. damascena
. Among these, the plastome of
A. glaucifolium
displays the highest average pairwise sequence divergence (0.2851) with
N. sativa
, followed by
A. raddeana
(0.2290) and
A. coerulea
(0.1222). Furthermore, the study identified 12 distinct hotspot regions characterized by elevated Pi values (> 0.1). These regions include
trn
H
-GUG-psb
A
, mat
K
-trn
Q
-UUG, psb
K
-trn
R
-UCU, atp
F
-atp
I
, rpo
B
-psb
D
, ycf3-ndh
J
, ndh
C
-cem
A
, pet
A
-psa
J
, trn
N-
GUU-ndh
F
, trn
V
-GAC-rps12, ycf2-trn
I
-CAU, and ndh
A
-ycf1
. Approximately, 24 tandem and 48 palindromic and forward repeats were detected in
N. sativa
plastome. The analysis revealed 32 microsatellites with the majority being mononucleotide repeats. In the
N. sativa
plastome, phenylalanine had the highest number of codons (1982 codons), while alanine was the least common amino acid with 260 codons. A phylogenetic tree, constructed using protein-coding genes, revealed a distinct monophyletic clade comprising
N. sativa
and
N. damascene
, closely aligned with the Cimicifugeae tribe and exhibiting robust support. This plastome provides valuable genetic information for precise species identification, phylogenetic resolution, and evolutionary studies of
N. sativa
. |
doi_str_mv | 10.1038/s41598-024-65073-6 |
format | article |
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Nigella sativa
(black seed), was analyzed for the first time. The plastome spans approximately 154,120 bp, comprising four sections: the Large Single-Copy (LSC) (85,538 bp), the Small Single-Copy (SSC) (17,984 bp), and two Inverted Repeat (IR) regions (25,299 bp). A comparative study of
N. sativa
’s plastome with ten other species from various genera in the Ranunculaceae family reveals substantial structural variations. The contraction of the inverted repeat region in
N. sativa
influences the boundaries of single-copy regions, resulting in a shorter plastome size than other species. When comparing the plastome of
N. sativa
with those of its related species, significant divergence is observed, particularly except for
N. damascena
. Among these, the plastome of
A. glaucifolium
displays the highest average pairwise sequence divergence (0.2851) with
N. sativa
, followed by
A. raddeana
(0.2290) and
A. coerulea
(0.1222). Furthermore, the study identified 12 distinct hotspot regions characterized by elevated Pi values (> 0.1). These regions include
trn
H
-GUG-psb
A
, mat
K
-trn
Q
-UUG, psb
K
-trn
R
-UCU, atp
F
-atp
I
, rpo
B
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D
, ycf3-ndh
J
, ndh
C
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A
, pet
A
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J
, trn
N-
GUU-ndh
F
, trn
V
-GAC-rps12, ycf2-trn
I
-CAU, and ndh
A
-ycf1
. Approximately, 24 tandem and 48 palindromic and forward repeats were detected in
N. sativa
plastome. The analysis revealed 32 microsatellites with the majority being mononucleotide repeats. In the
N. sativa
plastome, phenylalanine had the highest number of codons (1982 codons), while alanine was the least common amino acid with 260 codons. A phylogenetic tree, constructed using protein-coding genes, revealed a distinct monophyletic clade comprising
N. sativa
and
N. damascene
, closely aligned with the Cimicifugeae tribe and exhibiting robust support. This plastome provides valuable genetic information for precise species identification, phylogenetic resolution, and evolutionary studies of
N. sativa
.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-024-65073-6</identifier><identifier>PMID: 38914674</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/449 ; 631/449/2491 ; Amino acids ; Codons ; Comparative studies ; Divergence ; Genetic analysis ; Genome, Plastid ; Hotspot regions ; Humanities and Social Sciences ; Inverted repeat ; Microsatellites ; multidisciplinary ; N. sativa ; Nigella sativa ; Nigella sativa - chemistry ; Nigella sativa - genetics ; Phylogenetic study ; Phylogenetics ; Phylogeny ; Physical characteristics ; Plastome ; RpoB protein ; Science ; Science (multidisciplinary)</subject><ispartof>Scientific reports, 2024-06, Vol.14 (1), p.14509-16, Article 14509</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c366t-e18aa3bc32b731b06c73fdc6c8622e90a2ff4ddfb8ce2fc1ee7121dad7a41eed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3071635539/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3071635539?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25732,27903,27904,36991,36992,44569,74873</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38914674$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lubna</creatorcontrib><creatorcontrib>Asaf, Sajjad</creatorcontrib><creatorcontrib>Khan, Ibrahim</creatorcontrib><creatorcontrib>Jan, Rahmatullah</creatorcontrib><creatorcontrib>Asif, Saleem</creatorcontrib><creatorcontrib>Bilal, Saqib</creatorcontrib><creatorcontrib>Kim, Kyung-Min</creatorcontrib><creatorcontrib>AL-Harrasi, Ahmed</creatorcontrib><title>Genetic characterization and phylogenetic analysis of the Nigella sativa (black seed) plastome</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>In this study, the complete plastome sequence of
Nigella sativa
(black seed), was analyzed for the first time. The plastome spans approximately 154,120 bp, comprising four sections: the Large Single-Copy (LSC) (85,538 bp), the Small Single-Copy (SSC) (17,984 bp), and two Inverted Repeat (IR) regions (25,299 bp). A comparative study of
N. sativa
’s plastome with ten other species from various genera in the Ranunculaceae family reveals substantial structural variations. The contraction of the inverted repeat region in
N. sativa
influences the boundaries of single-copy regions, resulting in a shorter plastome size than other species. When comparing the plastome of
N. sativa
with those of its related species, significant divergence is observed, particularly except for
N. damascena
. Among these, the plastome of
A. glaucifolium
displays the highest average pairwise sequence divergence (0.2851) with
N. sativa
, followed by
A. raddeana
(0.2290) and
A. coerulea
(0.1222). Furthermore, the study identified 12 distinct hotspot regions characterized by elevated Pi values (> 0.1). These regions include
trn
H
-GUG-psb
A
, mat
K
-trn
Q
-UUG, psb
K
-trn
R
-UCU, atp
F
-atp
I
, rpo
B
-psb
D
, ycf3-ndh
J
, ndh
C
-cem
A
, pet
A
-psa
J
, trn
N-
GUU-ndh
F
, trn
V
-GAC-rps12, ycf2-trn
I
-CAU, and ndh
A
-ycf1
. Approximately, 24 tandem and 48 palindromic and forward repeats were detected in
N. sativa
plastome. The analysis revealed 32 microsatellites with the majority being mononucleotide repeats. In the
N. sativa
plastome, phenylalanine had the highest number of codons (1982 codons), while alanine was the least common amino acid with 260 codons. A phylogenetic tree, constructed using protein-coding genes, revealed a distinct monophyletic clade comprising
N. sativa
and
N. damascene
, closely aligned with the Cimicifugeae tribe and exhibiting robust support. This plastome provides valuable genetic information for precise species identification, phylogenetic resolution, and evolutionary studies of
N. sativa
.</description><subject>631/449</subject><subject>631/449/2491</subject><subject>Amino acids</subject><subject>Codons</subject><subject>Comparative studies</subject><subject>Divergence</subject><subject>Genetic analysis</subject><subject>Genome, Plastid</subject><subject>Hotspot regions</subject><subject>Humanities and Social Sciences</subject><subject>Inverted repeat</subject><subject>Microsatellites</subject><subject>multidisciplinary</subject><subject>N. sativa</subject><subject>Nigella sativa</subject><subject>Nigella sativa - chemistry</subject><subject>Nigella sativa - genetics</subject><subject>Phylogenetic study</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Physical characteristics</subject><subject>Plastome</subject><subject>RpoB protein</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kU1v1DAQhiMEolXpH-CALHEph4C_4sRHVNEPqYJLe8Ua2-PdLNl4sbNI21-Pd7MtiAO-2B4_83pm3qp6y-hHRkX3KUvW6K6mXNaqoa2o1YvqlFPZ1Fxw_vKv80l1nvOKltVwLZl-XZ2ITjOpWnlafb_GEafeEbeEBG7C1D_C1MeRwOjJZrkb4uJIwAjDLveZxECmJZKv_QKHAUgu_C8gF3YA94NkRP-BbAbIU1zjm-pVgCHj-XE_qx6uvtxf3tR3365vLz_f1U4oNdXIOgBhneC2FcxS5VoRvFOuU5yjpsBDkN4H2znkwTHElnHmwbcgy8WLs-p21vURVmaT-jWknYnQm0MgpoWBVJoY0ASLnbZWSsq8dNqB5QhtoE6DklrttS5mrU2KP7eYJ7Pus9u3OmLcZiNoyw_TbAv6_h90FbepzOlAMSWaRuhC8ZlyKeacMDwXyKjZm2lmM00x0xzMNKokvTtKb-0a_XPKk3UFEDOQy9O4wPTn7__I_gZmaqsx</recordid><startdate>20240624</startdate><enddate>20240624</enddate><creator>Lubna</creator><creator>Asaf, Sajjad</creator><creator>Khan, Ibrahim</creator><creator>Jan, Rahmatullah</creator><creator>Asif, Saleem</creator><creator>Bilal, Saqib</creator><creator>Kim, Kyung-Min</creator><creator>AL-Harrasi, Ahmed</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><general>Nature Portfolio</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>20240624</creationdate><title>Genetic characterization and phylogenetic analysis of the Nigella sativa (black seed) plastome</title><author>Lubna ; Asaf, Sajjad ; Khan, Ibrahim ; Jan, Rahmatullah ; Asif, Saleem ; Bilal, Saqib ; Kim, Kyung-Min ; AL-Harrasi, Ahmed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c366t-e18aa3bc32b731b06c73fdc6c8622e90a2ff4ddfb8ce2fc1ee7121dad7a41eed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>631/449</topic><topic>631/449/2491</topic><topic>Amino acids</topic><topic>Codons</topic><topic>Comparative studies</topic><topic>Divergence</topic><topic>Genetic analysis</topic><topic>Genome, Plastid</topic><topic>Hotspot regions</topic><topic>Humanities and Social Sciences</topic><topic>Inverted repeat</topic><topic>Microsatellites</topic><topic>multidisciplinary</topic><topic>N. sativa</topic><topic>Nigella sativa</topic><topic>Nigella sativa - chemistry</topic><topic>Nigella sativa - genetics</topic><topic>Phylogenetic study</topic><topic>Phylogenetics</topic><topic>Phylogeny</topic><topic>Physical characteristics</topic><topic>Plastome</topic><topic>RpoB protein</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lubna</creatorcontrib><creatorcontrib>Asaf, Sajjad</creatorcontrib><creatorcontrib>Khan, Ibrahim</creatorcontrib><creatorcontrib>Jan, Rahmatullah</creatorcontrib><creatorcontrib>Asif, Saleem</creatorcontrib><creatorcontrib>Bilal, Saqib</creatorcontrib><creatorcontrib>Kim, Kyung-Min</creatorcontrib><creatorcontrib>AL-Harrasi, Ahmed</creatorcontrib><collection>SpringerOpen(OpenAccess)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lubna</au><au>Asaf, Sajjad</au><au>Khan, Ibrahim</au><au>Jan, Rahmatullah</au><au>Asif, Saleem</au><au>Bilal, Saqib</au><au>Kim, Kyung-Min</au><au>AL-Harrasi, Ahmed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic characterization and phylogenetic analysis of the Nigella sativa (black seed) plastome</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2024-06-24</date><risdate>2024</risdate><volume>14</volume><issue>1</issue><spage>14509</spage><epage>16</epage><pages>14509-16</pages><artnum>14509</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>In this study, the complete plastome sequence of
Nigella sativa
(black seed), was analyzed for the first time. The plastome spans approximately 154,120 bp, comprising four sections: the Large Single-Copy (LSC) (85,538 bp), the Small Single-Copy (SSC) (17,984 bp), and two Inverted Repeat (IR) regions (25,299 bp). A comparative study of
N. sativa
’s plastome with ten other species from various genera in the Ranunculaceae family reveals substantial structural variations. The contraction of the inverted repeat region in
N. sativa
influences the boundaries of single-copy regions, resulting in a shorter plastome size than other species. When comparing the plastome of
N. sativa
with those of its related species, significant divergence is observed, particularly except for
N. damascena
. Among these, the plastome of
A. glaucifolium
displays the highest average pairwise sequence divergence (0.2851) with
N. sativa
, followed by
A. raddeana
(0.2290) and
A. coerulea
(0.1222). Furthermore, the study identified 12 distinct hotspot regions characterized by elevated Pi values (> 0.1). These regions include
trn
H
-GUG-psb
A
, mat
K
-trn
Q
-UUG, psb
K
-trn
R
-UCU, atp
F
-atp
I
, rpo
B
-psb
D
, ycf3-ndh
J
, ndh
C
-cem
A
, pet
A
-psa
J
, trn
N-
GUU-ndh
F
, trn
V
-GAC-rps12, ycf2-trn
I
-CAU, and ndh
A
-ycf1
. Approximately, 24 tandem and 48 palindromic and forward repeats were detected in
N. sativa
plastome. The analysis revealed 32 microsatellites with the majority being mononucleotide repeats. In the
N. sativa
plastome, phenylalanine had the highest number of codons (1982 codons), while alanine was the least common amino acid with 260 codons. A phylogenetic tree, constructed using protein-coding genes, revealed a distinct monophyletic clade comprising
N. sativa
and
N. damascene
, closely aligned with the Cimicifugeae tribe and exhibiting robust support. This plastome provides valuable genetic information for precise species identification, phylogenetic resolution, and evolutionary studies of
N. sativa
.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>38914674</pmid><doi>10.1038/s41598-024-65073-6</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
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ispartof | Scientific reports, 2024-06, Vol.14 (1), p.14509-16, Article 14509 |
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language | eng |
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source | Publicly Available Content Database; PubMed Central(OpenAccess); Full-Text Journals in Chemistry (Open access); Springer Nature - nature.com Journals - Fully Open Access |
subjects | 631/449 631/449/2491 Amino acids Codons Comparative studies Divergence Genetic analysis Genome, Plastid Hotspot regions Humanities and Social Sciences Inverted repeat Microsatellites multidisciplinary N. sativa Nigella sativa Nigella sativa - chemistry Nigella sativa - genetics Phylogenetic study Phylogenetics Phylogeny Physical characteristics Plastome RpoB protein Science Science (multidisciplinary) |
title | Genetic characterization and phylogenetic analysis of the Nigella sativa (black seed) plastome |
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