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Genetic and Physical Analyses of the Centromeric and Pericentromeric Regions of Human Chromosome 5: Recombination across 5cen

Identifieur interne : 001C94 ( Istex/Corpus ); précédent : 001C93; suivant : 001C95

Genetic and Physical Analyses of the Centromeric and Pericentromeric Regions of Human Chromosome 5: Recombination across 5cen

Auteurs : Jacques Puechberty ; Anne-Marie Laurent ; Sylvie Gimenez ; Alain Billault ; Marie-Elisabeth Brun-Laurent ; Alphonse Calenda ; Bertrand Marçais ; Catherine Prades ; Panos Ioannou ; Yuri Yurov ; Gérard Roizès

Source :

RBID : ISTEX:986C5480D98FC931F86EEBCDF1B123D61012259C

English descriptors

Abstract

Abstract: Human centromeres are poorly understood at both the genetic and the physical level. In this paper, we have been able to distinguish the alphoid centromeric sequences of chromosome 5 from those of chromosome 19. This result was obtained by pulsed-field gel electrophoresis after cutting genomic DNA with restriction endonucleasesNcoI (chromosome 5) andBamHI (chromosome 19). We could thus define a highly polymorphic marker, representing length variations of the D5Z1 domain located at the q arm boundary of the chromosome 5 centromere. The centromeric region of chromosome 5 was then analyzed in full detail. We established an approximately 4.6-Mb physical map of the whole region with five rare-cutting enzymes by using nonchimeric YACs, two of which were shown to contain the very ends of 5cen on both sides. The p-arm side of 5cen was shown to contain an alphoid subset (D5Z12) different from those described thus far. Two genes and several putative cDNAs could be precisely located close to the centromere. Several L1 elements were shown to be present within alpha satellites at the boundary between alphoid and nonalphoid sequences on both sides of 5cen. They were used to define STSs that could serve as physical anchor points at the junction of 5cen with the p and q arms. Some STSs were placed on a radiation hybrid map. One was polymorphic and could therefore be used as a second centromeric genetic marker at the p arm boundary of 5cen. We could thus estimate recombination rates within and around the centromeric region of chromosome 5. Recombination is highly reduced within 5cen, with zero recombinants in 58 meioses being detected between the two markers located at the two extremities of the centromere. In its immediate vicinity, 5cen indeed exerts a direct negative effect on meiotic recombination within the proximal chromosomal DNA. This effect is, however, less important than expected and is polarized, as different rates are observed on both arms if one compares the 0 cM/Mb of the p proximal first 5.5 Mb and the 0.64 cM/Mb of the q proximal first 5 Mb to the sex-average 1.02 cM/Mb found throughout the entire chromosome 5. Rates then become close to the average when one goes further within the arms. Finally, most recombinants (21/22), irrespective of the arm, are of female origin, thus showing that recombination around 5cen is essentially occurring in the female lineage.

Url:
DOI: 10.1006/geno.1999.5742

Links to Exploration step

ISTEX:986C5480D98FC931F86EEBCDF1B123D61012259C

Le document en format XML

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<div type="abstract" xml:lang="en">Abstract: Human centromeres are poorly understood at both the genetic and the physical level. In this paper, we have been able to distinguish the alphoid centromeric sequences of chromosome 5 from those of chromosome 19. This result was obtained by pulsed-field gel electrophoresis after cutting genomic DNA with restriction endonucleasesNcoI (chromosome 5) andBamHI (chromosome 19). We could thus define a highly polymorphic marker, representing length variations of the D5Z1 domain located at the q arm boundary of the chromosome 5 centromere. The centromeric region of chromosome 5 was then analyzed in full detail. We established an approximately 4.6-Mb physical map of the whole region with five rare-cutting enzymes by using nonchimeric YACs, two of which were shown to contain the very ends of 5cen on both sides. The p-arm side of 5cen was shown to contain an alphoid subset (D5Z12) different from those described thus far. Two genes and several putative cDNAs could be precisely located close to the centromere. Several L1 elements were shown to be present within alpha satellites at the boundary between alphoid and nonalphoid sequences on both sides of 5cen. They were used to define STSs that could serve as physical anchor points at the junction of 5cen with the p and q arms. Some STSs were placed on a radiation hybrid map. One was polymorphic and could therefore be used as a second centromeric genetic marker at the p arm boundary of 5cen. We could thus estimate recombination rates within and around the centromeric region of chromosome 5. Recombination is highly reduced within 5cen, with zero recombinants in 58 meioses being detected between the two markers located at the two extremities of the centromere. In its immediate vicinity, 5cen indeed exerts a direct negative effect on meiotic recombination within the proximal chromosomal DNA. This effect is, however, less important than expected and is polarized, as different rates are observed on both arms if one compares the 0 cM/Mb of the p proximal first 5.5 Mb and the 0.64 cM/Mb of the q proximal first 5 Mb to the sex-average 1.02 cM/Mb found throughout the entire chromosome 5. Rates then become close to the average when one goes further within the arms. Finally, most recombinants (21/22), irrespective of the arm, are of female origin, thus showing that recombination around 5cen is essentially occurring in the female lineage.</div>
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<ce:cross-ref refid="QA1">
<ce:sup>b</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:given-name>Marie-Elisabeth</ce:given-name>
<ce:surname>Brun-Laurent</ce:surname>
<ce:cross-ref refid="QA0">
<ce:sup>a</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:given-name>Alphonse</ce:given-name>
<ce:surname>Calenda</ce:surname>
<ce:cross-ref refid="QA0">
<ce:sup>a</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:given-name>Bertrand</ce:given-name>
<ce:surname>Marçais</ce:surname>
<ce:cross-ref refid="QA0">
<ce:sup>a</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:given-name>Catherine</ce:given-name>
<ce:surname>Prades</ce:surname>
<ce:cross-ref refid="QA0">
<ce:sup>a</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:given-name>Panos</ce:given-name>
<ce:surname>Ioannou</ce:surname>
<ce:cross-ref refid="QA2">
<ce:sup>c</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:given-name>Yuri</ce:given-name>
<ce:surname>Yurov</ce:surname>
<ce:cross-ref refid="QA0">
<ce:sup>a</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:given-name>Gérard</ce:given-name>
<ce:surname>Roizès</ce:surname>
<ce:cross-ref refid="QA0">
<ce:sup>a</ce:sup>
</ce:cross-ref>
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<ce:sup>1</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:affiliation id="QA0">
<ce:label>a</ce:label>
<ce:textfn>Séquences répétées et Centromères Humains, Institut de Génétique Humaine, CNRS UPR 1142, Institut de Biologie, 4 Boulevard Henri IV, 34060, Montpellier Cedex, France</ce:textfn>
</ce:affiliation>
<ce:affiliation id="QA1">
<ce:label>b</ce:label>
<ce:textfn>Centre d'Etude du Polymorphisme Humain, 27 Rue Juliette Dodu, 75010, Paris, France</ce:textfn>
</ce:affiliation>
<ce:affiliation id="QA2">
<ce:label>c</ce:label>
<ce:textfn>Gene Therapy Group, The Murdoch Institute for Research into Birth Defects, Royal Children's Hospital, Flemington Road, Parkville, Melbourne, Victoria, 3052, Australia</ce:textfn>
</ce:affiliation>
<ce:footnote id="QFN1">
<ce:label>1</ce:label>
<ce:note-para>To whom correspondence should be addressed. Telephone: 33 (0) 4.67.66.35.54. Fax: 33 (0) 4.67.66.03.06. E-mail:roizes@igh.cnrs.fr.</ce:note-para>
</ce:footnote>
</ce:author-group>
<ce:date-received day="2" month="11" year="1998"></ce:date-received>
<ce:date-accepted day="4" month="1" year="1999"></ce:date-accepted>
<ce:abstract>
<ce:section-title>Abstract</ce:section-title>
<ce:abstract-sec>
<ce:simple-para>Human centromeres are poorly understood at both the genetic and the physical level. In this paper, we have been able to distinguish the alphoid centromeric sequences of chromosome 5 from those of chromosome 19. This result was obtained by pulsed-field gel electrophoresis after cutting genomic DNA with restriction endonucleases
<ce:italic>Nco</ce:italic>
I (chromosome 5) and
<ce:italic>Bam</ce:italic>
HI (chromosome 19). We could thus define a highly polymorphic marker, representing length variations of the D5Z1 domain located at the q arm boundary of the chromosome 5 centromere. The centromeric region of chromosome 5 was then analyzed in full detail. We established an approximately 4.6-Mb physical map of the whole region with five rare-cutting enzymes by using nonchimeric YACs, two of which were shown to contain the very ends of 5cen on both sides. The p-arm side of 5cen was shown to contain an alphoid subset (D5Z12) different from those described thus far. Two genes and several putative cDNAs could be precisely located close to the centromere. Several L1 elements were shown to be present within alpha satellites at the boundary between alphoid and nonalphoid sequences on both sides of 5cen. They were used to define STSs that could serve as physical anchor points at the junction of 5cen with the p and q arms. Some STSs were placed on a radiation hybrid map. One was polymorphic and could therefore be used as a second centromeric genetic marker at the p arm boundary of 5cen. We could thus estimate recombination rates within and around the centromeric region of chromosome 5. Recombination is highly reduced within 5cen, with zero recombinants in 58 meioses being detected between the two markers located at the two extremities of the centromere. In its immediate vicinity, 5cen indeed exerts a direct negative effect on meiotic recombination within the proximal chromosomal DNA. This effect is, however, less important than expected and is polarized, as different rates are observed on both arms if one compares the 0 cM/Mb of the p proximal first 5.5 Mb and the 0.64 cM/Mb of the q proximal first 5 Mb to the sex-average 1.02 cM/Mb found throughout the entire chromosome 5. Rates then become close to the average when one goes further within the arms. Finally, most recombinants (21/22), irrespective of the arm, are of female origin, thus showing that recombination around 5cen is essentially occurring in the female lineage.</ce:simple-para>
</ce:abstract-sec>
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<affiliation>Séquences répétées et Centromères Humains, Institut de Génétique Humaine, CNRS UPR 1142, Institut de Biologie, 4 Boulevard Henri IV, 34060, Montpellier Cedex, France</affiliation>
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<affiliation>Séquences répétées et Centromères Humains, Institut de Génétique Humaine, CNRS UPR 1142, Institut de Biologie, 4 Boulevard Henri IV, 34060, Montpellier Cedex, France</affiliation>
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<role>
<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Alphonse</namePart>
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<affiliation>Séquences répétées et Centromères Humains, Institut de Génétique Humaine, CNRS UPR 1142, Institut de Biologie, 4 Boulevard Henri IV, 34060, Montpellier Cedex, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<affiliation>Séquences répétées et Centromères Humains, Institut de Génétique Humaine, CNRS UPR 1142, Institut de Biologie, 4 Boulevard Henri IV, 34060, Montpellier Cedex, France</affiliation>
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<description>To whom correspondence should be addressed. Telephone: 33 (0) 4.67.66.35.54. Fax: 33 (0) 4.67.66.03.06. E-mail:roizes@igh.cnrs.fr.</description>
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<abstract lang="en">Abstract: Human centromeres are poorly understood at both the genetic and the physical level. In this paper, we have been able to distinguish the alphoid centromeric sequences of chromosome 5 from those of chromosome 19. This result was obtained by pulsed-field gel electrophoresis after cutting genomic DNA with restriction endonucleasesNcoI (chromosome 5) andBamHI (chromosome 19). We could thus define a highly polymorphic marker, representing length variations of the D5Z1 domain located at the q arm boundary of the chromosome 5 centromere. The centromeric region of chromosome 5 was then analyzed in full detail. We established an approximately 4.6-Mb physical map of the whole region with five rare-cutting enzymes by using nonchimeric YACs, two of which were shown to contain the very ends of 5cen on both sides. The p-arm side of 5cen was shown to contain an alphoid subset (D5Z12) different from those described thus far. Two genes and several putative cDNAs could be precisely located close to the centromere. Several L1 elements were shown to be present within alpha satellites at the boundary between alphoid and nonalphoid sequences on both sides of 5cen. They were used to define STSs that could serve as physical anchor points at the junction of 5cen with the p and q arms. Some STSs were placed on a radiation hybrid map. One was polymorphic and could therefore be used as a second centromeric genetic marker at the p arm boundary of 5cen. We could thus estimate recombination rates within and around the centromeric region of chromosome 5. Recombination is highly reduced within 5cen, with zero recombinants in 58 meioses being detected between the two markers located at the two extremities of the centromere. In its immediate vicinity, 5cen indeed exerts a direct negative effect on meiotic recombination within the proximal chromosomal DNA. This effect is, however, less important than expected and is polarized, as different rates are observed on both arms if one compares the 0 cM/Mb of the p proximal first 5.5 Mb and the 0.64 cM/Mb of the q proximal first 5 Mb to the sex-average 1.02 cM/Mb found throughout the entire chromosome 5. Rates then become close to the average when one goes further within the arms. Finally, most recombinants (21/22), irrespective of the arm, are of female origin, thus showing that recombination around 5cen is essentially occurring in the female lineage.</abstract>
<note>Sequence data from this article have been deposited with the EMBL/GenBank/DDBJ Data Libraries under Accession Nos. AJ007751–AJ007762. The accession number for D5S2930 is AF023528. Genotypic data for D5S2930 and D5S2934 are available from the CEPH databasehttp://www.cephb.fr/cephdb).</note>
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