Fine scale mapping places DLG1, the gene encoding hDlg, telomeric to the OPA1 candidate region.

Fine scale mapping places DLG1, the gene encoding hDlg, telomeric to the OPA1 candidate region.
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精细尺度映射将编码 hDlg 的基因 DLG1、端粒定位到 OPA1 候选区域。

DOI:
10.1007/s003359900578
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发表时间:
1997
期刊:
Mammalian genome : official journal of the International Mammalian Genome Society
影响因子:
--
通讯作者:
Chishti,AH
Chishti,AH
中科院分区:
--
文献类型:
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作者:
Alexander,C;Stathakis,DG;Lin,L;Rahman,S;Bryant,PJ;Auburger,G;Chishti,AH

文献摘要

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Map position: proximal–D13Mit1–1.06 cM±1.06 SE–Mtr, D13Bir4, D13Bir6–1.06±1.06–D13Abb1e–2.13±1.49–D13Bir7–distal Method of mapping: Mtr was localized by RFLP analysis of 96 animals from an interspecific backcross panel ((C57BL/6JEi× SPRET/Ei) F1× SPRET/Ei) provided by The Jackson Laboratory, Bar Harbor, Me.(BSS panel)[1].Database deposit information: The data are available from the Mouse Genome Database, accession number MGD-JNUM-39061. Molecular reagents: A 1095-bp mouse cDNA was obtained by reverse transcription/PCR of mouse liver RNA, with degenerate oligonucleotides based on regions of homology within the methionine synthase sequences of lower organisms. The two primers (D1730 and D1733), as described by Leclerc et al.[2], were successful in amplifying both human and mouse cDNAs. The PCR products from both species were subcloned and sequenced; they showed 89% identity. The mouse cDNA was labeled by random priming and hybridized to Southern blots of EcoRI-digested mouse genomic DNA. Allele detection: Allele detection was performed by RFLP analysis of an EcoRI polymorphism. The C57BL/6J strain has alleles of approximately 13 kb, while the Mus spretus strain has alleles of approximately 9 kb and 4 kb. A constant band of approximately 0.5 kb was seen in both strains.