Genetic heterogeneity and ploidy level analysis among different gynogenetic clones of the polyploid gibel carp

Background Some triploid and tetraploid clones have been identified in the gynogenetic gibel carp, Carassius auratus gibelio Bloch, by karyotypic and cytologic analyses over many years. Further, 5–20% males and karyotypic diversity have been found among their natural and artificial populations. Howe...

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Veröffentlicht in:Cytometry. Part A 2003-11, Vol.56A (1), p.46-52
Hauptverfasser: Wei, Wen‐Hui, Zhang, Jing, Zhang, Yi‐Bing, Zhou, Li, Gui, Jian‐Fang
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creator Wei, Wen‐Hui
Zhang, Jing
Zhang, Yi‐Bing
Zhou, Li
Gui, Jian‐Fang
description Background Some triploid and tetraploid clones have been identified in the gynogenetic gibel carp, Carassius auratus gibelio Bloch, by karyotypic and cytologic analyses over many years. Further, 5–20% males and karyotypic diversity have been found among their natural and artificial populations. However, the DNA contents and the relation to their ploidy level and chromosome numbers have not been ascertained, and whether normal meiosis occurs in spermatogenesis needs to be determined in the different clones. Methods The sampled blood cells or sperms were mixed with blood cells from chicken or individual gibel carp and fixed in 70% pre‐cooled ethanol overnight at 4°C. The mixed cell pellets were washed 2–3 times in 1× phosphate buffered saline and then resuspended in the solution containing 0.5% pepsin and 0.1 M HCl. DNA was stained with propidium iodide solution (40 μg/mL) containing 4 kU/ml RNase. The measurements of DNA contents were performed with Phoenix Flow Systems. Results Triploid clones A, E, F, and P had almost equal DNA content, but triploid clone D had greater DNA content than did the other four triploid clones. DNA content of clone M (7.01 ± 0.15 pg/nucleus) was almost equal to the DNA content of clone D (5.38 ± 0.06 pg/nucleus) plus the DNA content of common carp sperm (1.64 ± 0.02 pg/nucleus). The DNA contents of sperms from clones A, P, and D were half of their blood cells, suggesting that normal meiosis occurs in spermatogenesis. Conclusions Flow cytometry is a powerful method to analyze genetic heterogeneity and ploidy level among different gynogenetic clones of polyploid gibel carp. Through this study, four questions have been answered. (a) The DNA content correlation among the five triploid clones and one multiple tetraploid clone was revealed in the gibel carp, and the contents increased with not only the ploidy level but also the chromosome number. (b) Mean DNA content was 0.052 pg in six extra chromosomes of clone D, which was higher than that of each chromosome in clones A, E, F, and P (about 0.032 pg/chromosome). This means that the six extra chromosomes are larger chromosomes. (c) Normal meiosis occurred during spermatogenesis of the gibel carp, because DNA contents of the sperms from clones A, P, and D were almost half of that in their blood cells. (d) Multiple tetraploid clone M (7.01 ± 0.15 pg/nucleus) contained the complete genome of clone D (5.38 ± 0.06 pg/nucleus) and the genome of common carp sperm (1.64 ± 0.02 pg/nucleus). C
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Further, 5–20% males and karyotypic diversity have been found among their natural and artificial populations. However, the DNA contents and the relation to their ploidy level and chromosome numbers have not been ascertained, and whether normal meiosis occurs in spermatogenesis needs to be determined in the different clones. Methods The sampled blood cells or sperms were mixed with blood cells from chicken or individual gibel carp and fixed in 70% pre‐cooled ethanol overnight at 4°C. The mixed cell pellets were washed 2–3 times in 1× phosphate buffered saline and then resuspended in the solution containing 0.5% pepsin and 0.1 M HCl. DNA was stained with propidium iodide solution (40 μg/mL) containing 4 kU/ml RNase. The measurements of DNA contents were performed with Phoenix Flow Systems. Results Triploid clones A, E, F, and P had almost equal DNA content, but triploid clone D had greater DNA content than did the other four triploid clones. DNA content of clone M (7.01 ± 0.15 pg/nucleus) was almost equal to the DNA content of clone D (5.38 ± 0.06 pg/nucleus) plus the DNA content of common carp sperm (1.64 ± 0.02 pg/nucleus). The DNA contents of sperms from clones A, P, and D were half of their blood cells, suggesting that normal meiosis occurs in spermatogenesis. Conclusions Flow cytometry is a powerful method to analyze genetic heterogeneity and ploidy level among different gynogenetic clones of polyploid gibel carp. Through this study, four questions have been answered. (a) The DNA content correlation among the five triploid clones and one multiple tetraploid clone was revealed in the gibel carp, and the contents increased with not only the ploidy level but also the chromosome number. (b) Mean DNA content was 0.052 pg in six extra chromosomes of clone D, which was higher than that of each chromosome in clones A, E, F, and P (about 0.032 pg/chromosome). This means that the six extra chromosomes are larger chromosomes. (c) Normal meiosis occurred during spermatogenesis of the gibel carp, because DNA contents of the sperms from clones A, P, and D were almost half of that in their blood cells. (d) Multiple tetraploid clone M (7.01 ± 0.15 pg/nucleus) contained the complete genome of clone D (5.38 ± 0.06 pg/nucleus) and the genome of common carp sperm (1.64 ± 0.02 pg/nucleus). Cytometry Part A 56A:46–52, 2003. © 2003 Wiley‐Liss, Inc.</description><identifier>ISSN: 1552-4922</identifier><identifier>EISSN: 1552-4930</identifier><identifier>DOI: 10.1002/cyto.a.10077</identifier><identifier>PMID: 14566938</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; blood cell ; Blood Cells - metabolism ; Carps ; Cell Nucleus - metabolism ; Chickens ; DNA - metabolism ; DNA content ; flow cytometry ; Flow Cytometry - methods ; Genetic Heterogeneity ; gibel carp ; Karyotyping ; Male ; Meiosis ; Ploidies ; polyploid ; sperm ; Spermatozoa - metabolism</subject><ispartof>Cytometry. 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Part A</title><addtitle>Cytometry A</addtitle><description>Background Some triploid and tetraploid clones have been identified in the gynogenetic gibel carp, Carassius auratus gibelio Bloch, by karyotypic and cytologic analyses over many years. Further, 5–20% males and karyotypic diversity have been found among their natural and artificial populations. However, the DNA contents and the relation to their ploidy level and chromosome numbers have not been ascertained, and whether normal meiosis occurs in spermatogenesis needs to be determined in the different clones. Methods The sampled blood cells or sperms were mixed with blood cells from chicken or individual gibel carp and fixed in 70% pre‐cooled ethanol overnight at 4°C. The mixed cell pellets were washed 2–3 times in 1× phosphate buffered saline and then resuspended in the solution containing 0.5% pepsin and 0.1 M HCl. DNA was stained with propidium iodide solution (40 μg/mL) containing 4 kU/ml RNase. The measurements of DNA contents were performed with Phoenix Flow Systems. Results Triploid clones A, E, F, and P had almost equal DNA content, but triploid clone D had greater DNA content than did the other four triploid clones. DNA content of clone M (7.01 ± 0.15 pg/nucleus) was almost equal to the DNA content of clone D (5.38 ± 0.06 pg/nucleus) plus the DNA content of common carp sperm (1.64 ± 0.02 pg/nucleus). The DNA contents of sperms from clones A, P, and D were half of their blood cells, suggesting that normal meiosis occurs in spermatogenesis. Conclusions Flow cytometry is a powerful method to analyze genetic heterogeneity and ploidy level among different gynogenetic clones of polyploid gibel carp. Through this study, four questions have been answered. (a) The DNA content correlation among the five triploid clones and one multiple tetraploid clone was revealed in the gibel carp, and the contents increased with not only the ploidy level but also the chromosome number. (b) Mean DNA content was 0.052 pg in six extra chromosomes of clone D, which was higher than that of each chromosome in clones A, E, F, and P (about 0.032 pg/chromosome). This means that the six extra chromosomes are larger chromosomes. (c) Normal meiosis occurred during spermatogenesis of the gibel carp, because DNA contents of the sperms from clones A, P, and D were almost half of that in their blood cells. (d) Multiple tetraploid clone M (7.01 ± 0.15 pg/nucleus) contained the complete genome of clone D (5.38 ± 0.06 pg/nucleus) and the genome of common carp sperm (1.64 ± 0.02 pg/nucleus). Cytometry Part A 56A:46–52, 2003. © 2003 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>blood cell</subject><subject>Blood Cells - metabolism</subject><subject>Carps</subject><subject>Cell Nucleus - metabolism</subject><subject>Chickens</subject><subject>DNA - metabolism</subject><subject>DNA content</subject><subject>flow cytometry</subject><subject>Flow Cytometry - methods</subject><subject>Genetic Heterogeneity</subject><subject>gibel carp</subject><subject>Karyotyping</subject><subject>Male</subject><subject>Meiosis</subject><subject>Ploidies</subject><subject>polyploid</subject><subject>sperm</subject><subject>Spermatozoa - metabolism</subject><issn>1552-4922</issn><issn>1552-4930</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAQhi0EoqWwMSNPTLT44iSuR1RBQULqUgYmy3HOrZEbhzgF5d-Tfgg2pvvQc490LyHXwCbAWHJvujZM9K4X4oQMIcuScSo5O_3tk2RALmL8YIxnjCfnZABplueST4ekmmOFrTN0jS02YdVPru2orkpa--DKjnr8Qt8vtO-ii1RvQrWipbMWG6xauuqq_dXOYXyoMNJgabtGWgff7R105YpeYXRTX5Izq33Eq2Mdkbenx-Xsefy6mL_MHl7HhnMQY2lzAJ0aI7VJWZFZAYLzEvpf8rSQWAjDpUmmUOQIYLmQrJQabFbIROgy4SNye_DWTfjcYmzVxkWD3usKwzYqARyA9c4RuTuApgkxNmhV3biNbjoFTO3yVbt8lVb7fHv85ujdFhss_-BjoD3AD8C389j9K1Oz9-XioP0BjiiJBw</recordid><startdate>200311</startdate><enddate>200311</enddate><creator>Wei, Wen‐Hui</creator><creator>Zhang, Jing</creator><creator>Zhang, Yi‐Bing</creator><creator>Zhou, Li</creator><creator>Gui, Jian‐Fang</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><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>7X8</scope></search><sort><creationdate>200311</creationdate><title>Genetic heterogeneity and ploidy level analysis among different gynogenetic clones of the polyploid gibel carp</title><author>Wei, Wen‐Hui ; Zhang, Jing ; Zhang, Yi‐Bing ; Zhou, Li ; Gui, Jian‐Fang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3317-9f611a4cc9ac40b5f71733d149264b9eb7c39c281b6e11f3790d9a1f5b927ad23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>blood cell</topic><topic>Blood Cells - metabolism</topic><topic>Carps</topic><topic>Cell Nucleus - metabolism</topic><topic>Chickens</topic><topic>DNA - metabolism</topic><topic>DNA content</topic><topic>flow cytometry</topic><topic>Flow Cytometry - methods</topic><topic>Genetic Heterogeneity</topic><topic>gibel carp</topic><topic>Karyotyping</topic><topic>Male</topic><topic>Meiosis</topic><topic>Ploidies</topic><topic>polyploid</topic><topic>sperm</topic><topic>Spermatozoa - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wei, Wen‐Hui</creatorcontrib><creatorcontrib>Zhang, Jing</creatorcontrib><creatorcontrib>Zhang, Yi‐Bing</creatorcontrib><creatorcontrib>Zhou, Li</creatorcontrib><creatorcontrib>Gui, Jian‐Fang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cytometry. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wei, Wen‐Hui</au><au>Zhang, Jing</au><au>Zhang, Yi‐Bing</au><au>Zhou, Li</au><au>Gui, Jian‐Fang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic heterogeneity and ploidy level analysis among different gynogenetic clones of the polyploid gibel carp</atitle><jtitle>Cytometry. Part A</jtitle><addtitle>Cytometry A</addtitle><date>2003-11</date><risdate>2003</risdate><volume>56A</volume><issue>1</issue><spage>46</spage><epage>52</epage><pages>46-52</pages><issn>1552-4922</issn><eissn>1552-4930</eissn><abstract>Background Some triploid and tetraploid clones have been identified in the gynogenetic gibel carp, Carassius auratus gibelio Bloch, by karyotypic and cytologic analyses over many years. Further, 5–20% males and karyotypic diversity have been found among their natural and artificial populations. However, the DNA contents and the relation to their ploidy level and chromosome numbers have not been ascertained, and whether normal meiosis occurs in spermatogenesis needs to be determined in the different clones. Methods The sampled blood cells or sperms were mixed with blood cells from chicken or individual gibel carp and fixed in 70% pre‐cooled ethanol overnight at 4°C. The mixed cell pellets were washed 2–3 times in 1× phosphate buffered saline and then resuspended in the solution containing 0.5% pepsin and 0.1 M HCl. DNA was stained with propidium iodide solution (40 μg/mL) containing 4 kU/ml RNase. The measurements of DNA contents were performed with Phoenix Flow Systems. Results Triploid clones A, E, F, and P had almost equal DNA content, but triploid clone D had greater DNA content than did the other four triploid clones. DNA content of clone M (7.01 ± 0.15 pg/nucleus) was almost equal to the DNA content of clone D (5.38 ± 0.06 pg/nucleus) plus the DNA content of common carp sperm (1.64 ± 0.02 pg/nucleus). The DNA contents of sperms from clones A, P, and D were half of their blood cells, suggesting that normal meiosis occurs in spermatogenesis. Conclusions Flow cytometry is a powerful method to analyze genetic heterogeneity and ploidy level among different gynogenetic clones of polyploid gibel carp. Through this study, four questions have been answered. (a) The DNA content correlation among the five triploid clones and one multiple tetraploid clone was revealed in the gibel carp, and the contents increased with not only the ploidy level but also the chromosome number. (b) Mean DNA content was 0.052 pg in six extra chromosomes of clone D, which was higher than that of each chromosome in clones A, E, F, and P (about 0.032 pg/chromosome). This means that the six extra chromosomes are larger chromosomes. (c) Normal meiosis occurred during spermatogenesis of the gibel carp, because DNA contents of the sperms from clones A, P, and D were almost half of that in their blood cells. (d) Multiple tetraploid clone M (7.01 ± 0.15 pg/nucleus) contained the complete genome of clone D (5.38 ± 0.06 pg/nucleus) and the genome of common carp sperm (1.64 ± 0.02 pg/nucleus). Cytometry Part A 56A:46–52, 2003. © 2003 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14566938</pmid><doi>10.1002/cyto.a.10077</doi><tpages>7</tpages></addata></record>
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subjects Animals
blood cell
Blood Cells - metabolism
Carps
Cell Nucleus - metabolism
Chickens
DNA - metabolism
DNA content
flow cytometry
Flow Cytometry - methods
Genetic Heterogeneity
gibel carp
Karyotyping
Male
Meiosis
Ploidies
polyploid
sperm
Spermatozoa - metabolism
title Genetic heterogeneity and ploidy level analysis among different gynogenetic clones of the polyploid gibel carp
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