MOESM8 of Recapitulation of gametic DNA methylation and its post-fertilization maintenance with reassembled DNA elements at the mouse Igf2/H19 locus
Additional file 8: Figure S8. Monoallelic gene expression pattern is recapitulated in LCb118 knock-in mice. Gene expression analysis of the endo-LCb118 (A) or endo-LCb (B) embryos. In order to distinguish parental origin of the alleles by using SNPs between inbred mouse strains, endo-LCb118 or -LCb...
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creator | Matsuzaki, Hitomi Kuramochi, Daichi Okamura, Eiichi Hirakawa, Katsuhiko Ushiki, Aki Tanimoto, Keiji |
description | Additional file 8: Figure S8. Monoallelic gene expression pattern is recapitulated in LCb118 knock-in mice. Gene expression analysis of the endo-LCb118 (A) or endo-LCb (B) embryos. In order to distinguish parental origin of the alleles by using SNPs between inbred mouse strains, endo-LCb118 or -LCb hetero-knock-in mice (H19 ICR/LCb118 or LCb; C57BL/6 J [B6] background) were mated with wild-type mice (H19 ICR/H19 ICR; JF1/Msf [JF1]), and offspring was obtained. Total RNA was prepared from livers of E12.5 embryos. Igf2 and H19 gene transcripts were amplified by RT-PCR (within logarithmic amplification range) with α-32P-labeled dCTP, followed by BstUI or Cac8I digestion, respectively. Parental origin of transcripts was discriminated by allele-specific restriction sites. The sites were also introduced into primer sequence so that complete digestion of PCR products can be concomitantly monitored. Gapdh gene transcript was analyzed as control. |
doi_str_mv | 10.6084/m9.figshare.11610969 |
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Monoallelic gene expression pattern is recapitulated in LCb118 knock-in mice. Gene expression analysis of the endo-LCb118 (A) or endo-LCb (B) embryos. In order to distinguish parental origin of the alleles by using SNPs between inbred mouse strains, endo-LCb118 or -LCb hetero-knock-in mice (H19 ICR/LCb118 or LCb; C57BL/6 J [B6] background) were mated with wild-type mice (H19 ICR/H19 ICR; JF1/Msf [JF1]), and offspring was obtained. Total RNA was prepared from livers of E12.5 embryos. Igf2 and H19 gene transcripts were amplified by RT-PCR (within logarithmic amplification range) with α-32P-labeled dCTP, followed by BstUI or Cac8I digestion, respectively. Parental origin of transcripts was discriminated by allele-specific restriction sites. The sites were also introduced into primer sequence so that complete digestion of PCR products can be concomitantly monitored. Gapdh gene transcript was analyzed as control.</description><identifier>DOI: 10.6084/m9.figshare.11610969</identifier><language>eng</language><publisher>figshare</publisher><subject>Biochemistry ; Cell Biology ; Computational Biology ; Developmental Biology ; FOS: Biological sciences ; FOS: Health sciences ; Genetics ; Hematology ; Infectious Diseases ; Marine Biology ; Medicine ; Molecular Biology ; Plant Biology</subject><creationdate>2020</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,1888</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.11610969$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Matsuzaki, Hitomi</creatorcontrib><creatorcontrib>Kuramochi, Daichi</creatorcontrib><creatorcontrib>Okamura, Eiichi</creatorcontrib><creatorcontrib>Hirakawa, Katsuhiko</creatorcontrib><creatorcontrib>Ushiki, Aki</creatorcontrib><creatorcontrib>Tanimoto, Keiji</creatorcontrib><title>MOESM8 of Recapitulation of gametic DNA methylation and its post-fertilization maintenance with reassembled DNA elements at the mouse Igf2/H19 locus</title><description>Additional file 8: Figure S8. Monoallelic gene expression pattern is recapitulated in LCb118 knock-in mice. Gene expression analysis of the endo-LCb118 (A) or endo-LCb (B) embryos. In order to distinguish parental origin of the alleles by using SNPs between inbred mouse strains, endo-LCb118 or -LCb hetero-knock-in mice (H19 ICR/LCb118 or LCb; C57BL/6 J [B6] background) were mated with wild-type mice (H19 ICR/H19 ICR; JF1/Msf [JF1]), and offspring was obtained. Total RNA was prepared from livers of E12.5 embryos. Igf2 and H19 gene transcripts were amplified by RT-PCR (within logarithmic amplification range) with α-32P-labeled dCTP, followed by BstUI or Cac8I digestion, respectively. Parental origin of transcripts was discriminated by allele-specific restriction sites. The sites were also introduced into primer sequence so that complete digestion of PCR products can be concomitantly monitored. Gapdh gene transcript was analyzed as control.</description><subject>Biochemistry</subject><subject>Cell Biology</subject><subject>Computational Biology</subject><subject>Developmental Biology</subject><subject>FOS: Biological sciences</subject><subject>FOS: Health sciences</subject><subject>Genetics</subject><subject>Hematology</subject><subject>Infectious Diseases</subject><subject>Marine Biology</subject><subject>Medicine</subject><subject>Molecular Biology</subject><subject>Plant Biology</subject><fulltext>true</fulltext><rsrctype>image</rsrctype><creationdate>2020</creationdate><recordtype>image</recordtype><sourceid>PQ8</sourceid><recordid>eNqdj81OwzAQhHPhgIA34LAv0DSGKqqPqC0qh4IE3K3FWScr-SeyN0LlOXhgWmhfgNOMZjQjfVV1q5q6bZaLedC1474MmKlWqlWNbvVl9b172bztlpAcvJLFkWXyKJziMekxkLCF9fMDHNywP1UYO2ApMKYiM0dZ2PPXXxWQo1DEaAk-WQbIhKVQ-PDU_f6Qp0DxMEYBGQhCmgrBU-_u5lulwSc7levqwqEvdHPSq2rxuHlfbWcdCloWMmPmgHlvVGOOcCZoc4YzZ7j7f85-AKRWZGE</recordid><startdate>20200115</startdate><enddate>20200115</enddate><creator>Matsuzaki, Hitomi</creator><creator>Kuramochi, Daichi</creator><creator>Okamura, Eiichi</creator><creator>Hirakawa, Katsuhiko</creator><creator>Ushiki, Aki</creator><creator>Tanimoto, Keiji</creator><general>figshare</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20200115</creationdate><title>MOESM8 of Recapitulation of gametic DNA methylation and its post-fertilization maintenance with reassembled DNA elements at the mouse Igf2/H19 locus</title><author>Matsuzaki, Hitomi ; Kuramochi, Daichi ; Okamura, Eiichi ; Hirakawa, Katsuhiko ; Ushiki, Aki ; Tanimoto, Keiji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_6084_m9_figshare_116109693</frbrgroupid><rsrctype>images</rsrctype><prefilter>images</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Biochemistry</topic><topic>Cell Biology</topic><topic>Computational Biology</topic><topic>Developmental Biology</topic><topic>FOS: Biological sciences</topic><topic>FOS: Health sciences</topic><topic>Genetics</topic><topic>Hematology</topic><topic>Infectious Diseases</topic><topic>Marine Biology</topic><topic>Medicine</topic><topic>Molecular Biology</topic><topic>Plant Biology</topic><toplevel>online_resources</toplevel><creatorcontrib>Matsuzaki, Hitomi</creatorcontrib><creatorcontrib>Kuramochi, Daichi</creatorcontrib><creatorcontrib>Okamura, Eiichi</creatorcontrib><creatorcontrib>Hirakawa, Katsuhiko</creatorcontrib><creatorcontrib>Ushiki, Aki</creatorcontrib><creatorcontrib>Tanimoto, Keiji</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Matsuzaki, Hitomi</au><au>Kuramochi, Daichi</au><au>Okamura, Eiichi</au><au>Hirakawa, Katsuhiko</au><au>Ushiki, Aki</au><au>Tanimoto, Keiji</au><format>book</format><genre>unknown</genre><ristype>GEN</ristype><title>MOESM8 of Recapitulation of gametic DNA methylation and its post-fertilization maintenance with reassembled DNA elements at the mouse Igf2/H19 locus</title><date>2020-01-15</date><risdate>2020</risdate><abstract>Additional file 8: Figure S8. Monoallelic gene expression pattern is recapitulated in LCb118 knock-in mice. Gene expression analysis of the endo-LCb118 (A) or endo-LCb (B) embryos. In order to distinguish parental origin of the alleles by using SNPs between inbred mouse strains, endo-LCb118 or -LCb hetero-knock-in mice (H19 ICR/LCb118 or LCb; C57BL/6 J [B6] background) were mated with wild-type mice (H19 ICR/H19 ICR; JF1/Msf [JF1]), and offspring was obtained. Total RNA was prepared from livers of E12.5 embryos. Igf2 and H19 gene transcripts were amplified by RT-PCR (within logarithmic amplification range) with α-32P-labeled dCTP, followed by BstUI or Cac8I digestion, respectively. Parental origin of transcripts was discriminated by allele-specific restriction sites. The sites were also introduced into primer sequence so that complete digestion of PCR products can be concomitantly monitored. Gapdh gene transcript was analyzed as control.</abstract><pub>figshare</pub><doi>10.6084/m9.figshare.11610969</doi><oa>free_for_read</oa></addata></record> |
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subjects | Biochemistry Cell Biology Computational Biology Developmental Biology FOS: Biological sciences FOS: Health sciences Genetics Hematology Infectious Diseases Marine Biology Medicine Molecular Biology Plant Biology |
title | MOESM8 of Recapitulation of gametic DNA methylation and its post-fertilization maintenance with reassembled DNA elements at the mouse Igf2/H19 locus |
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