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Detection of ploidy and chromosomal aberrations in commercial oil palm using high-throughput SNP markers
Main conclusion Karyotyping using high-density genome-wide SNP markers identified various chromosomal aberrations in oil palm ( Elaeis guineensis Jacq.) with supporting evidence from the 2C DNA content measurements (determined using FCM) and chromosome counts. Oil palm produces a quarter of the worl...
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Published in: | Planta 2021-02, Vol.253 (2), p.63-63, Article 63 |
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creator | Ngoot-Chin, Ting Zulkifli, Muhammad Azwan van de Weg, Eric Zaki, Noorhariza Mohd Serdari, Norhalida Mohamed Mustaffa, Suzana Zainol Abidin, Mohd Isa Sanusi, Nik Shazana Nik Mohd Smulders, Marinus J. M. Low, Eng Ti Leslie Ithnin, Maizura Singh, Rajinder |
description | Main conclusion
Karyotyping using high-density genome-wide SNP markers identified various chromosomal aberrations in oil palm (
Elaeis guineensis
Jacq.) with supporting evidence from the 2C DNA content measurements (determined using FCM) and chromosome counts.
Oil palm produces a quarter of the world’s total vegetable oil. In line with its global importance, an initiative to sequence the oil palm genome was carried out successfully, producing huge amounts of sequence information, allowing SNP discovery. High-capacity SNP genotyping platforms have been widely used for marker–trait association studies in oil palm. Besides genotyping, a SNP array is also an attractive tool for understanding aberrations in chromosome inheritance. Exploiting this, the present study utilized chromosome-wide SNP allelic distributions to determine the ploidy composition of over 1,000 oil palms from a commercial F
1
family, including 197 derived from twin-embryo seeds. Our method consisted of an inspection of the allelic intensity ratio using SNP markers. For palms with a shifted or abnormal distribution ratio, the SNP allelic frequencies were plotted along the pseudo-chromosomes. This method proved to be efficient in identifying whole genome duplication (triploids) and aneuploidy. We also detected several loss of heterozygosity regions which may indicate small chromosomal deletions and/or inheritance of identical by descent regions from both parents. The SNP analysis was validated by flow cytometry and chromosome counts. The triploids were all derived from twin-embryo seeds. This is the first report on the efficiency and reliability of SNP array data for karyotyping oil palm chromosomes, as an alternative to the conventional cytogenetic technique. Information on the ploidy composition and chromosomal structural variation can help to better understand the genetic makeup of samples and lead to a more robust interpretation of the genomic data in marker–trait association analyses. |
doi_str_mv | 10.1007/s00425-021-03567-7 |
format | article |
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Karyotyping using high-density genome-wide SNP markers identified various chromosomal aberrations in oil palm (
Elaeis guineensis
Jacq.) with supporting evidence from the 2C DNA content measurements (determined using FCM) and chromosome counts.
Oil palm produces a quarter of the world’s total vegetable oil. In line with its global importance, an initiative to sequence the oil palm genome was carried out successfully, producing huge amounts of sequence information, allowing SNP discovery. High-capacity SNP genotyping platforms have been widely used for marker–trait association studies in oil palm. Besides genotyping, a SNP array is also an attractive tool for understanding aberrations in chromosome inheritance. Exploiting this, the present study utilized chromosome-wide SNP allelic distributions to determine the ploidy composition of over 1,000 oil palms from a commercial F
1
family, including 197 derived from twin-embryo seeds. Our method consisted of an inspection of the allelic intensity ratio using SNP markers. For palms with a shifted or abnormal distribution ratio, the SNP allelic frequencies were plotted along the pseudo-chromosomes. This method proved to be efficient in identifying whole genome duplication (triploids) and aneuploidy. We also detected several loss of heterozygosity regions which may indicate small chromosomal deletions and/or inheritance of identical by descent regions from both parents. The SNP analysis was validated by flow cytometry and chromosome counts. The triploids were all derived from twin-embryo seeds. This is the first report on the efficiency and reliability of SNP array data for karyotyping oil palm chromosomes, as an alternative to the conventional cytogenetic technique. Information on the ploidy composition and chromosomal structural variation can help to better understand the genetic makeup of samples and lead to a more robust interpretation of the genomic data in marker–trait association analyses.</description><identifier>ISSN: 0032-0935</identifier><identifier>EISSN: 1432-2048</identifier><identifier>DOI: 10.1007/s00425-021-03567-7</identifier><identifier>PMID: 33544231</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Agriculture ; Aneuploidy ; Arecaceae - genetics ; Arrays ; Biomedical and Life Sciences ; Chromosome Aberrations ; Chromosome Mapping ; Chromosomes ; Chromosomes, Plant ; Composition ; Cytogenetics ; Deoxyribonucleic acid ; DNA ; Ecology ; Elaeis guineensis ; Embryos ; Flow cytometry ; Forestry ; Genomes ; Genotyping ; Heredity ; Heterozygosity ; High-Throughput Nucleotide Sequencing ; Inspection ; Life Sciences ; Loss of heterozygosity ; Markers ; Microsatellite Repeats ; Nucleotide sequence ; Original Article ; Plant Sciences ; Ploidies ; Ploidy ; Reproducibility of Results ; Seeds ; Single-nucleotide polymorphism ; Vegetable oils</subject><ispartof>Planta, 2021-02, Vol.253 (2), p.63-63, Article 63</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature 2021</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-a08c7535147400b981b371983ee1601eba1a49fe997aaf5139fe77768d0412483</citedby><cites>FETCH-LOGICAL-c375t-a08c7535147400b981b371983ee1601eba1a49fe997aaf5139fe77768d0412483</cites><orcidid>0000-0001-9933-4884</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33544231$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ngoot-Chin, Ting</creatorcontrib><creatorcontrib>Zulkifli, Muhammad Azwan</creatorcontrib><creatorcontrib>van de Weg, Eric</creatorcontrib><creatorcontrib>Zaki, Noorhariza Mohd</creatorcontrib><creatorcontrib>Serdari, Norhalida Mohamed</creatorcontrib><creatorcontrib>Mustaffa, Suzana</creatorcontrib><creatorcontrib>Zainol Abidin, Mohd Isa</creatorcontrib><creatorcontrib>Sanusi, Nik Shazana Nik Mohd</creatorcontrib><creatorcontrib>Smulders, Marinus J. M.</creatorcontrib><creatorcontrib>Low, Eng Ti Leslie</creatorcontrib><creatorcontrib>Ithnin, Maizura</creatorcontrib><creatorcontrib>Singh, Rajinder</creatorcontrib><title>Detection of ploidy and chromosomal aberrations in commercial oil palm using high-throughput SNP markers</title><title>Planta</title><addtitle>Planta</addtitle><addtitle>Planta</addtitle><description>Main conclusion
Karyotyping using high-density genome-wide SNP markers identified various chromosomal aberrations in oil palm (
Elaeis guineensis
Jacq.) with supporting evidence from the 2C DNA content measurements (determined using FCM) and chromosome counts.
Oil palm produces a quarter of the world’s total vegetable oil. In line with its global importance, an initiative to sequence the oil palm genome was carried out successfully, producing huge amounts of sequence information, allowing SNP discovery. High-capacity SNP genotyping platforms have been widely used for marker–trait association studies in oil palm. Besides genotyping, a SNP array is also an attractive tool for understanding aberrations in chromosome inheritance. Exploiting this, the present study utilized chromosome-wide SNP allelic distributions to determine the ploidy composition of over 1,000 oil palms from a commercial F
1
family, including 197 derived from twin-embryo seeds. Our method consisted of an inspection of the allelic intensity ratio using SNP markers. For palms with a shifted or abnormal distribution ratio, the SNP allelic frequencies were plotted along the pseudo-chromosomes. This method proved to be efficient in identifying whole genome duplication (triploids) and aneuploidy. We also detected several loss of heterozygosity regions which may indicate small chromosomal deletions and/or inheritance of identical by descent regions from both parents. The SNP analysis was validated by flow cytometry and chromosome counts. The triploids were all derived from twin-embryo seeds. This is the first report on the efficiency and reliability of SNP array data for karyotyping oil palm chromosomes, as an alternative to the conventional cytogenetic technique. Information on the ploidy composition and chromosomal structural variation can help to better understand the genetic makeup of samples and lead to a more robust interpretation of the genomic data in marker–trait association analyses.</description><subject>Agriculture</subject><subject>Aneuploidy</subject><subject>Arecaceae - genetics</subject><subject>Arrays</subject><subject>Biomedical and Life Sciences</subject><subject>Chromosome Aberrations</subject><subject>Chromosome Mapping</subject><subject>Chromosomes</subject><subject>Chromosomes, Plant</subject><subject>Composition</subject><subject>Cytogenetics</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Ecology</subject><subject>Elaeis guineensis</subject><subject>Embryos</subject><subject>Flow cytometry</subject><subject>Forestry</subject><subject>Genomes</subject><subject>Genotyping</subject><subject>Heredity</subject><subject>Heterozygosity</subject><subject>High-Throughput Nucleotide Sequencing</subject><subject>Inspection</subject><subject>Life Sciences</subject><subject>Loss of heterozygosity</subject><subject>Markers</subject><subject>Microsatellite Repeats</subject><subject>Nucleotide sequence</subject><subject>Original Article</subject><subject>Plant Sciences</subject><subject>Ploidies</subject><subject>Ploidy</subject><subject>Reproducibility of Results</subject><subject>Seeds</subject><subject>Single-nucleotide polymorphism</subject><subject>Vegetable oils</subject><issn>0032-0935</issn><issn>1432-2048</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kc1OxCAUhYnROOPoC7gwJG7cVC8FSrs0429i1ERdE9qhU8a2VGgX8_YydtTEhStucr5zgHsQOiZwTgDEhQdgMY8gJhFQnohI7KApYTSOYmDpLpoChBkyyifowPsVQBCF2EcTSjljMSVTVF3pXhe9sS22Je5qaxZrrNoFLipnG-tto2qscu2c2kAemxYXtmm0K0xQrKlxp-oGD960S1yZZRX1wTksq27o8cvjM26Ue9fOH6K9UtVeH23PGXq7uX6d30UPT7f388uHqKCC95GCtBCccsIEA8izlORUkCylWpMEiM4VUSwrdZYJpUpOaJiFEEm6AEZiltIZOhtzO2c_Bu172Rhf6LpWrbaDl4ERhKdhKwE9_YOu7ODa8LoNlSQxgSwJVDxShbPeO13KzpnwqbUkIDc9yLEHGXqQXz1IEUwn2-ghb_Tix_K9-ADQEfBBapfa_d79T-wnK6-SPg</recordid><startdate>20210205</startdate><enddate>20210205</enddate><creator>Ngoot-Chin, Ting</creator><creator>Zulkifli, Muhammad Azwan</creator><creator>van de Weg, Eric</creator><creator>Zaki, Noorhariza Mohd</creator><creator>Serdari, Norhalida Mohamed</creator><creator>Mustaffa, Suzana</creator><creator>Zainol Abidin, Mohd Isa</creator><creator>Sanusi, Nik Shazana Nik Mohd</creator><creator>Smulders, Marinus J. 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M. ; Low, Eng Ti Leslie ; Ithnin, Maizura ; Singh, Rajinder</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-a08c7535147400b981b371983ee1601eba1a49fe997aaf5139fe77768d0412483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Agriculture</topic><topic>Aneuploidy</topic><topic>Arecaceae - genetics</topic><topic>Arrays</topic><topic>Biomedical and Life Sciences</topic><topic>Chromosome Aberrations</topic><topic>Chromosome Mapping</topic><topic>Chromosomes</topic><topic>Chromosomes, Plant</topic><topic>Composition</topic><topic>Cytogenetics</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Ecology</topic><topic>Elaeis guineensis</topic><topic>Embryos</topic><topic>Flow cytometry</topic><topic>Forestry</topic><topic>Genomes</topic><topic>Genotyping</topic><topic>Heredity</topic><topic>Heterozygosity</topic><topic>High-Throughput Nucleotide Sequencing</topic><topic>Inspection</topic><topic>Life Sciences</topic><topic>Loss of heterozygosity</topic><topic>Markers</topic><topic>Microsatellite Repeats</topic><topic>Nucleotide sequence</topic><topic>Original Article</topic><topic>Plant Sciences</topic><topic>Ploidies</topic><topic>Ploidy</topic><topic>Reproducibility of Results</topic><topic>Seeds</topic><topic>Single-nucleotide polymorphism</topic><topic>Vegetable oils</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ngoot-Chin, Ting</creatorcontrib><creatorcontrib>Zulkifli, Muhammad Azwan</creatorcontrib><creatorcontrib>van de Weg, Eric</creatorcontrib><creatorcontrib>Zaki, Noorhariza Mohd</creatorcontrib><creatorcontrib>Serdari, Norhalida Mohamed</creatorcontrib><creatorcontrib>Mustaffa, Suzana</creatorcontrib><creatorcontrib>Zainol Abidin, Mohd Isa</creatorcontrib><creatorcontrib>Sanusi, Nik Shazana Nik Mohd</creatorcontrib><creatorcontrib>Smulders, Marinus J. M.</creatorcontrib><creatorcontrib>Low, Eng Ti Leslie</creatorcontrib><creatorcontrib>Ithnin, Maizura</creatorcontrib><creatorcontrib>Singh, Rajinder</creatorcontrib><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>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Agricultural Science Collection</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>ProQuest Pharma Collection</collection><collection>Technology Research Database</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 Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Databases</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</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>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Planta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ngoot-Chin, Ting</au><au>Zulkifli, Muhammad Azwan</au><au>van de Weg, Eric</au><au>Zaki, Noorhariza Mohd</au><au>Serdari, Norhalida Mohamed</au><au>Mustaffa, Suzana</au><au>Zainol Abidin, Mohd Isa</au><au>Sanusi, Nik Shazana Nik Mohd</au><au>Smulders, Marinus J. M.</au><au>Low, Eng Ti Leslie</au><au>Ithnin, Maizura</au><au>Singh, Rajinder</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of ploidy and chromosomal aberrations in commercial oil palm using high-throughput SNP markers</atitle><jtitle>Planta</jtitle><stitle>Planta</stitle><addtitle>Planta</addtitle><date>2021-02-05</date><risdate>2021</risdate><volume>253</volume><issue>2</issue><spage>63</spage><epage>63</epage><pages>63-63</pages><artnum>63</artnum><issn>0032-0935</issn><eissn>1432-2048</eissn><abstract>Main conclusion
Karyotyping using high-density genome-wide SNP markers identified various chromosomal aberrations in oil palm (
Elaeis guineensis
Jacq.) with supporting evidence from the 2C DNA content measurements (determined using FCM) and chromosome counts.
Oil palm produces a quarter of the world’s total vegetable oil. In line with its global importance, an initiative to sequence the oil palm genome was carried out successfully, producing huge amounts of sequence information, allowing SNP discovery. High-capacity SNP genotyping platforms have been widely used for marker–trait association studies in oil palm. Besides genotyping, a SNP array is also an attractive tool for understanding aberrations in chromosome inheritance. Exploiting this, the present study utilized chromosome-wide SNP allelic distributions to determine the ploidy composition of over 1,000 oil palms from a commercial F
1
family, including 197 derived from twin-embryo seeds. Our method consisted of an inspection of the allelic intensity ratio using SNP markers. For palms with a shifted or abnormal distribution ratio, the SNP allelic frequencies were plotted along the pseudo-chromosomes. This method proved to be efficient in identifying whole genome duplication (triploids) and aneuploidy. We also detected several loss of heterozygosity regions which may indicate small chromosomal deletions and/or inheritance of identical by descent regions from both parents. The SNP analysis was validated by flow cytometry and chromosome counts. The triploids were all derived from twin-embryo seeds. This is the first report on the efficiency and reliability of SNP array data for karyotyping oil palm chromosomes, as an alternative to the conventional cytogenetic technique. Information on the ploidy composition and chromosomal structural variation can help to better understand the genetic makeup of samples and lead to a more robust interpretation of the genomic data in marker–trait association analyses.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>33544231</pmid><doi>10.1007/s00425-021-03567-7</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-9933-4884</orcidid></addata></record> |
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subjects | Agriculture Aneuploidy Arecaceae - genetics Arrays Biomedical and Life Sciences Chromosome Aberrations Chromosome Mapping Chromosomes Chromosomes, Plant Composition Cytogenetics Deoxyribonucleic acid DNA Ecology Elaeis guineensis Embryos Flow cytometry Forestry Genomes Genotyping Heredity Heterozygosity High-Throughput Nucleotide Sequencing Inspection Life Sciences Loss of heterozygosity Markers Microsatellite Repeats Nucleotide sequence Original Article Plant Sciences Ploidies Ploidy Reproducibility of Results Seeds Single-nucleotide polymorphism Vegetable oils |
title | Detection of ploidy and chromosomal aberrations in commercial oil palm using high-throughput SNP markers |
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