Skip to main content

Table 1 Alternative 3′ ends for Olfr1507 and Olfr15 revealed in silico, and their subsequent experimental validation

From: Alternative polyadenylation produces multiple 3’ untranslated regions of odorant receptor mRNAs in mouse olfactory sensory neurons

 

RNA-Seq

RL-PAT

Gene

PolyA site

3’end position (nt after stop)

Matching canonical PAS (nt after stop)b

Cleavage position (nt after stop)

Nb of clones sequenced

PolyA tail length (nt, mean ± SEM)

Matching canonical PAS (nt after stop)e

Olfr1507

XS

Not detected

Not relevant

92

2

19 ± 8

None

114

2

17 ± 3

S

1193–1273a

AAUAAA (1263, 1281)

1283

7

44 ± 18

AAUAAA (1263, 1281)

1290

1

11

1294

1

39

M

2593

AUUAAA (2628)

2653

1

86

AUUAAA (2628)

L

4013

AAUAAA (4076)

4093

1

16

AAUAAA (4076)

4109

2

16 ± 1

4112

1

46

XL

4943

AAUAAA (5049)c

No RL-PAT confirmationd

Not relevant

Olfr15

S

902

AAUAAA (901)

924

2

87 ± 1

AAUAAA (901)

931

1

26

936

1

19

M1

2462

AUUAAA (2487), AAUAAA (2529)

No RL-PAT confirmationd

Not relevant

M2

2742

AAUAAA (2665, 2675, 2685, 2806, 2798, 2806, 2814, 2822), AUUAAA (2790)

2816

1

22

AAUAAA (2798, 2806, 2814, 2822), AUUAAA (2790)

2820

1

28

2824

1

31

2836

1

48

L

4762-4837a

AUUAAA (4717)

No RL-PAT confirmationd

Not relevant

  1. aThe 3’ ends distant of less than 100 nt were merged as a single polyA site. bFor each putative polyA site, predicted canonical PAS matching in a [− 100;+ 100] window from the RNA-Seq-deduced 3′ end are indicated. cNote that for Olfr1507 3’XL isoform, the closest canonical PAS is slightly outside the 100-nt precision window. The cleavage site and polyA tail length were experimentally mapped using RL-PAT on adult male OM, further confirming the polyA site usage for most of the 3’UTR isoforms. dXL site of Olfr1507, M1 and L sites of Olfr15 could not be confirmed by RL-PAT because no specific forward primer could be designed due to repeat sequences upstream of these polyA sites. eFor each confirmed polyA site, predicted canonical PAS matching in a [− 100;0] window from the identified cleavage sites are indicated