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. 2006 Jun;26(12):4410–4420. doi: 10.1128/MCB.02258-05

TABLE 4.

Distribution of macroH2A1 on subtraction clones

Clone(s) Malea Femalea Repeat(s) presentb Chromosome(s) Nearest gene
Forward subtraction clones
    1 2.7 ± 1.89 5.4 ± 0.65 MaLR LTR and LINE L1 1 Trpm8, intron
    5 2.1 ± 0.34 2.1 ± 0.2 Abuts an MaLR LTR 13 LOC432934, >100 kb
    8 4.1 ± 0.49 4.1 ± 0.24 GT repeat 4 Bach2, 15 kb
    13 5.8 ± 0.56 6.6 ± 0.84 MIR 6 Atp2b2, intron
    24 6.0 ± 0.66 7.7 ± 0.83 GT repeat and MIR 9 Edg8, 8.3 kb
    26 5.2 ± 0.6 5.3 ± 0.17 Flanked by MaLR and ERVL LTRs 11 1700019I23Rik, 27 kb
    27 5.0 ± 1.04 5.6 ± 0.3 MaLR LTR 2 Gm356, 14 kb
    28 3.8 ± 0.36 4.2 ± 0.7 RLTR4-int LTR Multiple Reverse transcriptase
    15, 18, 21 7.4 ± 0.24c 9.3 ± 0.56c 31-bp tandem repeat X, Y, 9, 13 Mid1 and others
    29 3.1 ± 0.16 3.2 ± 0.01 MER1 and MIR 6 LOC269739, 19 kb
    32 3.1 ± 0.17 3.5 ± 0.28 MaLR LTR and LINE L1 1 Cnih3, intron
Reverse subtraction clones
    O5 0.2 ± 0.02 0.8 ± 0.57 Repeated on Y and X Y and X
    O7 0.5 ± 0.11 0.7 ± 0.09 LINE L1 Multiple
    H2 0.6 ± 0.07 0.7 ± 0.05 LINE L1 Multiple
a

Values are ratios of the concentrations in the macroH2A1-enriched thiopropyl Sepharose eluted fractions to the concentrations in the starting materials, determined by real-time PCR. All target sequences were nonrepetitive except for clone 28 and the reverse subtraction clones.

b

Repeats were identified by Repeat Masker (50).

c

Result for a region 900 bp downstream of Mid1 between two clusters of these repeats.